Photodynamic therapy of cervical cancer: a scoping review on the efficacy of various molecules

Abstract

Background:

Cervical cancer poses a considerable worldwide health issue, where infection with the human papillomavirus (HPV) plays a vital role as a risk factor. Photodynamic therapy (PDT) is a minimally invasive treatment for HPV-related cervical lesions, which uses photosensitizers and light to selectively destroy abnormal cells.

Objectives:

Our objective is to present a comprehensive overview of the different types of molecules employed in PDT to reduce the occurrence and fatality rates associated with cervical cancer.

Design:

Scoping review and bibliometric analysis.

Methods:

The article explores clinical trials investigating the efficacy of PDT in treating low-grade squamous intraepithelial lesion and high-grade squamous intraepithelial lesion, as well as preclinical approaches utilizing various molecules for PDT in cervical cancer. Furthermore, the article sheds light on potential molecules for PDT enhancement, examining their properties through computer modeling simulations, molecular docking, and assessing their advantages and disadvantages.

Results:

Our findings demonstrate that PDT holds promise as a therapeutic approach for treating cervical lesions associated with HPV and cervical cancer. Additionally, we observe that the utilization of diverse dye classes enhances the anticancer effects of PDT.

Conclusion:

Among the various molecules employed in PDT, functionalized fullerene exhibits a notable inclination toward overexpressed receptors in cervical cancer cells, making it a potential candidate for intensified use in PDT. However, further research is needed to evaluate its long-term effectiveness and safety.

Plain language summary

Using light to treat cervical cancer: what you need to know

Cervical cancer is a significant global health concern, often linked to the human papillomavirus (HPV). There is a less invasive treatment called photodynamic therapy (PDT), which employs light and special substances to target and destroy abnormal cells related to HPV. In this review, we aim to give you a comprehensive look at the different substances used in PDT to reduce the occurrence and severity of cervical cancer. We have examined clinical trials focusing on treating specific types of cervical lesions and explored preclinical approaches using various substances. We have also delved into computer simulations and molecular docking to understand the strengths and weaknesses of these substances. Our findings show that PDT has potential as a treatment for HPV-related cervical lesions and cancer. Different dye classes used in this therapy enhance its effectiveness against cancer. Notably, a substance called functionalized fullerene stands out for its tendency to target receptors overexpressed in cervical cancer cells. It looks promising, but more research is necessary to ensure its long-term effectiveness and safety.

Keywords

bibliometric analysis cervical cancer human papillomavirus molecular docking photodynamic therapy squamous intraepithelial neoplasia

Introduction

Cervical cancer ranks among the leading causes of cancer-related fatalities among women worldwide.¹ The presence of human papillomavirus (HPV) represents a significant contributing factor to the development of cervical cancer.² Traditional treatment methods often encounter challenges in identifying and managing precursor lesions that precede the onset of cancer. The cervix’s cell lining can give rise to various precancerous cervical intraepithelial neoplasia (CIN), including CIN1, CIN2, and CIN3, and high-grade squamous intraepithelial lesion (HSIL), and low-grade squamous intraepithelial lesion (LSIL)³ (Table 1). LSIL denotes the mildest form of these lesions, while CIN2 falls in an intermediate category, and CIN3 signifies the most severe condition.⁴ HSIL encompasses both CIN2 and CIN3 and is considered a high-risk precursor to cervical cancer.⁵ If left untreated, HSIL poses a higher likelihood of progressing to cancer compared to LSIL or CIN1.⁶

Table 1.

Different types of cervical cancer based on histology indices³.

Abnormality	Description	Histology	Risk of progression
LSIL	Low-grade squamous intraepithelial lesion	CIN1	Low
CIN1	Cervical intraepithelial neoplasia 1	Mild dysplasia	Low
CIN2	Cervical intraepithelial neoplasia 2	Moderate dysplasia	Moderate
CIN3	Cervical intraepithelial neoplasia 3	Severe dysplasia/carcinoma in situ	High
HSIL	High-grade squamous intraepithelial lesion	CIN2–CIN3	High
ASC-US	Atypical squamous cells of undetermined significance	–	–
ASC-H	Atypical squamous cells, cannot exclude HSIL	–	–

To tackle this obstacle, scientists have devised an innovative technology aimed at enhancing the efficiency of treating underlying and precancerous lesions of the cervix linked to HPV.⁷ This technology leverages photodynamic therapy (PDT), a minimally invasive therapeutic method that employs photosensitizers and light to specifically target and eliminate abnormal cells.⁷ The novel approach incorporates a combination of a fluorescent dye and a specialized imaging system, facilitating real-time visualization of cervical lesions.^8,9 During the procedure, the cervix is coated with the photosensitizer, and subsequently, the targeted region is exposed to light of a specific wavelength.¹⁰ This process triggers the photosensitizer to generate reactive oxygen species, which selectively eradicate abnormal cells.¹¹ By precisely targeting the affected cells, this technique mitigates the risk of harm to healthy tissue, thereby enhancing treatment efficacy.¹² Furthermore, the utilized imaging system guarantees accurate and effective identification of cervical lesions correlated with HPV.¹³ Timely detection of these lesions via this technology holds the potential for enhanced treatment interventions and superior patient outcomes.^8,14

By enhancing the precision and efficacy of treatment, this technology holds the potential to decrease the global incidence and mortality rates of cervical cancer. The selection of an appropriate dye is a crucial aspect of PDT development. Over the years, various molecules have been employed in this technique. However, it is imperative to identify and assess these molecules to develop new photosensitizers that offer higher anticancer potency and greater convenience of use.¹⁵

This article aims to provide an overview of the potential advantages of PDT in reducing the occurrence and fatality rates associated with cervical cancer. We will summarize the safety and efficacy of PDT in patients with high-risk LSIL of the cervix, cervical ectropion, high-risk HPV infection, and postmenopausal women with persistent HPV infection and/or CIN1. Cervical ectropion is a benign condition considered a normal variant observed in women within the reproductive age group. In this state, the columnar epithelium, consisting of glandular cells, which typically lines the endocervix, extends onto the ectocervix, resulting in the exposure of these columnar cells to the vaginal environment.

To accomplish this, we conducted a bibliometric analysis to investigate the utilization of PDT for cervical cancer treatment. Numerous studies exploring the applications of PDT in this domain have been examined, with a focus on photochemotherapy, nanoparticles, and photosensitizing agents. Furthermore, we aimed to identify the molecules with the highest binding affinity to overexpressed receptors in cervical cancer cells, suggesting their potential as promising agents for PDT use.

Methods

Data collection and extraction for bibliometric analysis

Eligibility criteria and data source

In January 2024, an evaluation was carried out on the Scopus and Web of Science online databases to pinpoint the frequently employed keywords related to the use of PDT in the treatment of cervical cancer. We acquired all pertinent metadata in BibTeX format from Scopus and in text format from Web of Science. Subsequently, the data were consolidated using RStudio through a merging code (Supplemental Table S1) and saved as an Excel file (Supplemental Excel File).

Search strategy

In this scientific inquiry, an in-depth exploration was carried out in the Scopus and Web of Science databases utilizing advanced search functionalities. We utilized a blend of Boolean and Wildcard search operators to identify pertinent keywords for our study, as outlined in Supplemental Tables S2 and S3. The search was executed in January 2024, and the comprehensive search strategy is elucidated in Figure 1. Articles deemed irrelevant based on their titles, abstracts, and full-text content were systematically excluded. Subsequently, research articles were imported for bibliometric analyses from the obtained results.

Figure 1.

Flowchart for selecting articles in the bibliometric analysis of applications of PDT in treating cervical cancer.

Bibliometric analyses

Data management and bibliometric analysis were executed utilizing the bibliometric package (version 4.1.3) and Biblioshiny web applications within RStudio (RStudio 2023.09.1+494, PBC, Boston, MA). The analytical scope encompassed a 40-year timeframe for research articles, concentrating on publication and citation metrics, as well as citation trends.^16,17 Prolific institutions were discerned based on the quantity of articles related to the applications of PDT in treating cervical cancer.

Furthermore, collaborative networks were established among 582 leading research institutes using clustering algorithms and data normalization from 297 research articles, guided by an association parameter. Authors with noteworthy contributions were identified based on the frequency of their published articles. The evaluation also involved pinpointing the top 10 most frequently cited documents and leading journals.

This investigation delved into interactions among 10 prominent journals, fields of study, and countries contributing to research on the applications of PDT in treating cervical cancer. To depict global research collaboration, connections were visualized on a world map. A TreeMap visualization portrayed the 10 most frequently used keywords in articles published on this topic. Lastly, a ‘Thematic Map’ categorized topics into four domains: primary subjects, specialized subjects, emerging or declining subjects, and overarching foundational subjects.

Molecular interactions and docking studies of receptors that are overexpressed in cervical cancer cells and various molecules that are used in PDT

The identification of nine receptors that exhibit overexpression on the surface of cervical cancer cells was derived from previous studies including folate receptor α (FRα),¹⁸ transferrin receptor 1 (TR1),¹⁹ epidermal growth factor receptor (EGFR),²⁰ CD44,²¹ prominin 1 (CD133),²² vascular endothelial growth factor receptor 2 (VEGFR2),²³ vascular cell adhesion molecule-1 (VCAM-1),²⁴ aminopeptidase-N (CD13),²⁵ and biotin receptor (BR).²⁶

To evaluate the binding affinity between the mentioned receptors and various molecules used in PDT, AutoDock Vina²⁷ was employed. The 3D structures of the 19 molecules and nine receptors, namely, FRα, TR1, EGFR, CD44, VEGFR2, VCAM-1, CD13, BR, and CD133, were obtained from the PubChem²⁸ and Protein Data Bank (PDB) databases. The corresponding PDB codes for these receptors were 4km6, 2nsu, 7sye, 1poz, 2met, 1vsc, 4fyq, 5n7x, and UniRef90_O43490²¹ for CD133.

Following that, the receptors were remodeled using the SWISS-MODEL Server.²⁹ Nonpolar hydrogens and ionic pairs were merged, and Gasteiger partial charges were assigned to each ligand atom. Grid boxes were generated using the Computed Atlas of Surface Topography of Proteins (CASTp 3.0). Subsequently, docking was performed, resulting in nine conformations for each receptor and dye pair. The docking conformations were ranked based on their binding affinity, and the conformation with the lowest negative energy and an Root Mean Square Deviation (RMSD) value of ⩽2 Å was selected as the optimal conformation.

Visualization of intermolecular interaction

The PyMOL software (The PyMOL Molecular Graphics System, Version 1.2r3pre, Schrödinger, LLC., New York, USA) was utilized for visualizing the 3D structure of the optimal conformations. Furthermore, the detailed information regarding intermolecular interactions between the ligand and receptor was presented in a 2D format using Discovery Studio Visualizer.

In addition to the aforementioned analyses, we will address the limitations and future directions of PDT in treating cervical lesions. This includes an evaluation of the current clinical applications of PDT and a discussion of preclinical studies involving different molecules. We will also explore potential molecules for future studies on PDT application for cervical cancer, as well as evaluate the suitability of certain compounds as molecules for PDT through in silico simulations. Lastly, we will discuss the existing challenges and propose potential solutions for the application of PDT in cervical cancer treatment.

Data collection and extraction for systematic analysis of molecules for PDT of cervical cancer

Furthermore, an exhaustive and methodical literature exploration was undertaken to identify pertinent articles concentrating on the application of PDT for treating cervical lesions linked to HPV. The search spanned electronic databases, including Scopus and Web of Science, with a specific focus on articles published in the English language.

The search strategy incorporated the use of specific keywords such as ‘photodynamic therapy’, ‘cervical cancer’, ‘cervical lesions’, ‘human papillomavirus’, ‘HPV’, ‘precancerous lesions’, ‘dye’, ‘photosensitizer’, and ‘cervix’. These keywords were combined using appropriate Boolean operators (AND, OR) to refine the search outcomes. Initially, the titles and abstracts of the retrieved articles were scrutinized to identify potentially relevant studies. Subsequently, the full text of these articles was meticulously examined to ascertain their eligibility for inclusion in the analysis. Additionally, a manual exploration of the reference lists of relevant articles was conducted to uncover any additional studies meeting the predefined inclusion criteria.

The inclusion of articles in this assessment adhered to specific criteria, encompassing: (a) studies investigating the safety and efficacy of PDT in treating HPV-associated cervical lesions, (b) studies involving patients with high-risk LSIL of the cervix, cervical ectropion, high-risk HPV infection, postmenopausal women with persistent HPV infection, and/or CIN, and (c) studies published in peer-reviewed journals. Two independent reviewers conducted the article screening, and any disparities were resolved through discussion between the reviewers.

Results

Bibliometric analysis for PDT of cervical cancer

The analysis conducted using Biblioshiny classified the 297 studies (Figure 2). The findings, which explored the applications of PDT in the treatment of cervical cancer cells, revealed that ‘photodynamic therapy’ emerged as the most frequently encountered author keywords to date (Figure 3).

Figure 2.

The number of studies on photodynamic therapy in the field of treating cervical cancer cells.

Figure 3.

The most 10 frequent author keywords that have been used in the field of the usages of photo dynamic therapy in the field of treating cervical cancer cells.

Most contributing authors and their collaboration network

In our investigation of the PDT of cervical cancer, we analyzed the number of documents authored by different researchers. Among the most contributing authors of research articles, as shown in Supplemental Figure S1, Zhang Y had the highest number of articles (n = 18).

Most productive journals

Among the published articles in the field of our concern, 10 research articles were featured in the journal ‘Photodiagnosis and Photodynamic Therapy’ followed by 55 research articles in the journal, as shown in Supplemental Figure S3.

World research production

Supplemental Figure S3A illustrates the highest scholarly output related to the PDT of cervical cancer, China with emerging as the top production among the 33 countries. In our bibliometric analysis, the China emerges as the most cited country in research articles on PDT of cervical cancer (Supplemental Figure S3B).

Fullerenes, aluminum phthalocyanine chloride, and zinc phthalocyanine binding affinity to overexpressed receptors in cervical cancer cells

According to the data presented in Table 2, fullerenes demonstrated the strongest binding affinity to VEGFR, VCAM1, CD44, EGFR, and TR1 (Table 2). On the other side, aluminum phthalocyanine chloride and zinc phthalocyanine displayed the most in silico tendency to BR, CD13, and CD133 (Table 2). On the other hand, aluminum phthalocyanine chloride showed the most binding affinity to FR (Table 2). Furthermore, Figure 4 provides a visual representation of the molecules involved in the binding interactions between fullerenes, aluminum phthalocyanine chloride, and zinc phthalocyanine and mentioned receptors. The two-dimensional structures of all three remarked compounds, displaying its highest affinity to the mentioned receptors, are depicted in Figure 5.

Table 2.

The affinity of molecules that have been used in photodynamic therapy to the receptors that are overexpressed in cervical cancer cells (Kcal/mole).

Dye	Receptor
Dye	FRα*	TR1	EGFR	CD13	CD44	CD133	VCAM-1	VEGFR	BR
5-Aminolevulinic acid	−5.0	−4.9	−4.0	−4.4	−4.4	−2.8	−3.5	−3.1	−5.1
Protoporphyrin IX	−7.8	−8.3	−8.0	−10.4	−7.2	−5.0	−6.4	−5.7	−7.8
Hematoporphyrin	−8.2	−8.3	−8.0	−10.7	−7.3	−5.3	−6.2	−5.7	−7.8
Zinc phthalocyanine	−12.1	−12.2	−10.7	−13.2	−10.1	−6.8	−8.9	−7.5	−10.6
Chlorin e6	−7.4	−7.6	−8.4	−8.6	−6.5	−5.2	−7.0	−5.6	−6.7
Talaporfin Sodium	−7.4	−7.7	−6.8	−9.1	−7.3	−4.5	−5.9	−5.0	−6.8
Indocyanine Green (ICG)	−8.4	−9.5	−9.5	−10.5	−6.9	−6.0	−6.1	−6.4	−8.2
Rose Bengal	−6.6	−6.6	−7.0	−8.2	−6.2	−4.3	−5.9	−4.9	−6.4
Photofrin	−8.3	−8.0	−7.9	−10.0	−7.4	−5.2	−6.8	−5.9	−7.9
Hypericin	−10.3	−8.7	−8.9	−12.5	−8.3	−5.9	−8.7	−6.6	−9.0
Methylene Blue	−7.6	−7.3	−7.5	−7.3	−5.8	−4.4	−6.2	−4.5	−6.2
Curcumin	−7.2	−8.1	−7.0	−7.7	−6.2	−4.6	−5.8	−4.9	−6.8
Texaphyrin	−8.8	−8.5	−8.8	−10.0	−7.5	−5.6	−7.4	−6.0	−8.9
Bacteriochlorin	−8.2	−8.5	−7.1	−9.2	−7.5	−5.6	−6.6	−5.5	−8.2
Fullerene	−10.7	−13.7	−11.8	−11.0	−12.9	−6.4	−9.7	−9.3	−10.2
Eosin	−7.7	−7.4	−6.9	−8.4	−7.3	−5.0	−6.0	−5.6	−7.0
Erythrosine	−8.2	−7.8	−6.8	−8.6	−7.7	−4.9	−6.3	−5.6	−7.3
Methyl Violet	−8.7	−6.5	−7.3	−6.9	−5.9	−5.6	−6.0	−5.9	−6.3
Aluminum phthalocyanine chloride	−12.5	−12.8	−10.5	−13.2	−9.8	−6.8	−9.1	−8.3	−10.6

BR, Biotin receptor, CD13, Aminopeptidase-N, CD133, Prominin 1, EGFR, Epidermal growth factor receptor, FRα, Folate receptor α, TR1, Transferrin receptor 1, VCAM-1, vascular cell adhesion molecule 1, VEGFR, vascular endothelial growth factor receptor.

Figure 4.

The molecules and interactions that are involved in the binding site of best binding conformation fullerene, zinc phthalocyanine, and aluminum phthalocyanine chloride and the overexpressed receptors in cervical cancer. The interactions between all three mentioned receptors and following receptors: folate receptor α (FRα), Transferrin receptor 1 (TR1), epidermal growth factor receptor (EGFR), aminopeptidase-N (CD13), CD44, prominin 1 (CD133), vascular cell adhesion molecule 1 (VCAM-1), vascular endothelial growth factor receptor (VEGFR), and biotin receptor (BR) are demonstrated in detail.

Figure 5.

The 2D structure of fullerene, zinc phthalocyanine, and aluminum phthalocyanine chloride.

Clinical trials for PDT for LSIL

Numerous clinical trials, pilot studies, retrospective analyses, and prospective studies have explored the application of PDT for treating LSIL, employing various photosensitizing molecules (Table 3). These clinical trials have demonstrated promising outcomes when utilizing different photosensitizing molecules, such as 5-aminolevulinic acid (ALA), aluminum phthalocyanine chloride, photofrin, hexaminolevulinate, talaporfin sodium, and chlorin e6, for LSIL treatment. However, further investigations are necessary to validate the effectiveness and safety of these treatments and establish the optimal treatment parameters.

Table 3.

Treatment of low-grade squamous intraepithelial lesion (LSIL) with photodynamic therapy.

Dye	Patients	CR (%)	Type	Country	References
5-Aminolevulinic acid	115	79.0	Phase III	China Hungary Germany Slovakia	30
	48	88.6	Retrospective	China	31
	110	81.8	Prospective	China	32
	97	92.0	Prospective	China	33
	51	79.4	Prospective	Japan	34
	176	84.7	Pilot	China	35
	46	65.2	Retrospective	China	36
	30	73.3	Retrospective	China	37
	66	75.0	Retrospective	BrazilUSA	38
	39	76.9	Prospective	China	39
	12	33.0	Prospective	UK	40
	22	63.6	Prospective	China	41
	79	90.7	Prospective	China	42
	44	88.6	Retrospective	China	31
	30	80.0	Prospective	Mexico	43
	55	90.0	Retrospective	China	36
Aluminum phthalocyanine chloride	11	91.7	Prospective	Brazil	44
Chlorin e6	18	88.9	Prospective	China	45
	18	100	Prospective	Russia	7
Chlorin e6 + Photofrin	28	82.0	Retrospective	Russia	46
Hexaminolevulinate	262	95.0	Phase II	GermanyNorway	47
Photofrin	105	90.0	Prospective	Japan	48
Talaporfin sodium	9	88.9	Prospective	Japan	49

CR, complete response.

Clinical trials for PDT for HSIL

HSIL represents a more advanced stage of precancerous lesions with an elevated risk of developing into cervical cancer. Numerous molecules have undergone clinical trials (Table 4) to assess their suitability for PDT in treating HSIL, including ALA, chlorin e6, porphyrin, and hexaminolevulinate. While these molecules have exhibited promising outcomes in terms of complete response rates, they have also been associated with higher recurrence rates when compared to surgical interventions like Cold Knife Cone. Further investigation is warranted to enhance the efficacy and safety of PDT for HSIL.

Table 4.

Treatment of high-grade squamous intraepithelial lesion (HSIL) with photodynamic therapy.

Dye	Patients	CR (%)	Date	Type	Country	References
5-Aminolevulinic acid	148	86.5	2022	Retrospective	China	50
	32	31.0	2002	Phase I & II	United States	51
	7	42.0	1999	Prospective	Germany	52
	8	50.0	2021	Prospective	China	41
	5	80.0	2010	Prospective	China	53
	68	88.2	2022	Retrospective	China	54
	183	71.0	2022	Prospective	China	55
	96	89.5	2022	Retrospective	China	56
	99	88.9	2022	Retrospective	China	57
Porphyrin	20	91.0	2016	Retrospective	Korea	58
	88	53.4	2010	Prospective	Belarus	59
	46	87.0	2013	Retrospective	Korea	60
	34	97.1	2022	Retrospective	Korea	61
	49	90.4	2008	Prospective	Russia	62
	28	90.0	2003	Prospective	Japan	63
Chlorin e6	18	72.2	2022	Prospective	China	45
	24	70.0	2022	Prospective	Russia	7
Hexaminolevulinate	24	63.0	2008	Prospective	Germany	64

As per the records available on clinicaltrials.gov, out of the 591 registered studies on PDT for various cancer types up until the end of March 2023, only seven studies were specifically focused on cervical cancer. The relevant details of these studies can be found in Table 5. By analyzing the information gathered from clinicaltrials.gov (Table 5) along with the published clinical articles provided in Tables 4 and 5, we generated Figures 6 and 7. Figure 6 illustrates the frequency of dye applications in cervical cancer PDT, with ALA being the most commonly used. Additionally, Figure 7 reveals that China is at the forefront in terms of conducting clinical studies on PDT for cervical cancer.

Table 5.

Clinical trials on of treatment of cervical cancer with photodynamic therapy during 1999–2023 (U.S. National Library of Medicine).

Dye	NCT number	Type of cancer	Status	Country	Start date	Phase
Lutetium texaphyrin	NCT00005808	CIN 2 & 3	Terminated	United States	2000	I
Taporfin sodium	NCT00028405	CIN	Completed	United States	2001	I
Aminolaevulinic acid	NCT00369018	CIN	Completed	Germany Norway	2006	I & II
	NCT00708942	CIN	Terminated	FranceGermany Norway	2009	II
	NCT01256424	CIN	Completed	GermanyNorway	2011	II
	NCT02304770	Persistent High-Risk HPV InfectionCIN	Completed	China	2015	II
	NCT02631863	CINLSILPapillomavirus Infections	Completed	China	2016	II
	NCT04484415	CIN 2 & 3	Completed	China	2022	III

Figure 6.

Frequency of application of molecules for photodynamic therapy of cervical cancer during 1999–2023 in clinical trials.

Figure 7.

Frequency of country contributions in clinical trials on photodynamic therapy of cervical cancer during 1999–2023.

Discussion

PDT as a novel approach for cervical cancer therapy

While previous studies have acknowledged the advantages of PDT in the treatment of cervical cancer,⁶ our analysis revealed a decline in the number of studies focusing on the application of PDT for this purpose since 2022. This outcome (Figure 2) contradicts the findings reported in earlier research.

Photochemotherapy author keywords in the field of the usages of PDT for treating cervical cancer cells

This study revealed that photo chemotherapy emerged as the most frequently used MeSH author keywords in the context of PDT applications for treating cervical cancer cells. In other words, scientists have sought to enhance the effectiveness of anticancer treatment for cervical cancer by combining PDT with chemotherapy.⁶⁵ Our findings align with this result, supporting the notion that researchers have focused on improving the delivery of photosensitizing agents to enhance PDT efficacy.

Fullerenes, aluminum phthalocyanine chloride, and zinc phthalocyanine affinity on overexpressed receptors in cervical cancer

Previous studies have highlighted the efforts of scientists to enhance the delivery of photosensitizers to cancer cells, aiming to improve the efficacy of PDT.⁶⁶ Additionally, these studies have indicated that overexpressed receptors on the surface of cancer cells can serve as potential binding sites for photosensitizers.⁶⁶ Consequently, photosensitizers that exhibit a stronger tendency to attach to these overexpressed receptors facilitate their own delivery to cancer cells.⁶⁶ Thus, photosensitizers demonstrating a higher affinity for these receptors can be considered promising candidates for PDT. Through our in silico analysis, we found that fullerenes, aluminum phthalocyanine chloride, and zinc phthalocyanine displayed the highest affinity for overexpressed receptors in cervical cancer cells (Table 3). Therefore, these three identified candidates exhibit substantial potential as photosensitizers for PDT in the management of cervical cancer. However, further in vitro and in vivo studies are necessary to validate this finding.

Approved molecules for clinical approaches of PDT of cervical cancer

There are various types of molecules utilized in clinical studies of PDT for cervical cancer:

(A) 5-aminolevulinic acid: ALA is a photosensitizer employed in PDT for cervical cancer.⁶⁷ Several clinical trials have assessed the safety and efficacy of ALA-PDT in patients with CIN (Tables 4 and 5). Additional clinical studies are necessary to evaluate the long-term effectiveness of ALA-PDT in cervical cancer treatment.

(B) Aluminum phthalocyanine chloride: A second-generation photosensitizer, is utilized in PDT for various cancers, including cervical cancer.⁴⁴ Further clinical studies are required to evaluate the long-term efficacy of aluminum phthalocyanine chloride-mediated PDT in cervical cancer treatment.

(C) Photofrin: A photosensitizer approved for use in PDT for multiple cancers, including cervical cancer.⁶⁷ Additional clinical studies are needed to assess the long-term effectiveness of photofrin-mediated PDT in treating cervical cancer.

(D) Hexaminolevulinate: A photosensitizer employed in PDT for different cancers, including cervical cancer.⁶⁷ Further clinical studies are necessary to evaluate the long-term efficacy of hexaminolevulinate-mediated PDT in cervical cancer treatment.

(E) Talaporfin sodium: A photosensitizer approved for use in PDT for various cancers, including cervical cancer.⁴⁹ Studies have indicated that talaporfin-based PDT can be effective for cervical cancer treatment.⁶⁵

(F) Chlorin e6: Another photosensitizer used in PDT for cervical cancer.⁴⁵ It exhibits a high absorption rate in the near-infrared region, enabling deeper tissue penetration compared to other photosensitizers. Chlorin e6 has also demonstrated high selectivity for cancer cells over healthy cells, making it a promising candidate for PDT.⁶⁸

(G) Porphyrin derivatives: Derivatives, such as protoporphyrin IX and hematoporphyrin derivatives, are natural photosensitizers employed in PDT for cervical cancer.⁶³ These compounds naturally occur in the body and have shown higher accumulation rates in cancer cells than in healthy cells. When exposed to light of a specific wavelength, these photosensitizers generate reactive oxygen species capable of destroying cancer cells.⁶⁹

(H) Texaphyrins: Synthetic molecules investigated for their potential use in PDT for various cancers, including cervical cancer.⁷⁰ Preclinical studies have indicated that texaphyrin-based PDT can effectively induce cell death in cancer cells.⁷¹

Preclinical approaches of PDT of cervical cancer

Other types of molecules have shown promise for PDT in cervical cancer based on preclinical studies, but further research is necessary to evaluate their safety and effectiveness in human trials, as indicated in Table 6.

(A) Curcumin: A natural polyphenol compound found in turmeric. It has demonstrated anticancer properties.⁷² Studies have explored the use of curcumin-based PDT for cervical cancer.⁷³

(B) Hypericin: A compound present in St. John’s wort. It possesses photosensitizing properties and has been utilized in PDT for cervical cancer.⁷⁴ Upon activation by light, hypericin generates reactive oxygen species capable of damaging cancer cells. In vitro and animal studies have shown the effectiveness of hypericin in killing cancer cells,⁷⁵ but further investigation is required to assess its efficacy in humans.

(C) Indocyanine green (ICG): A water-soluble near-infrared dye that has been employed in PDT for various cancers, including cervical cancer.⁷⁶ Preclinical studies have indicated the potential use of ICG for PDT in cervical cancer.⁷⁷

(D) Methylene blue: A blue dye that has been utilized in medicine for several years. It has demonstrated effectiveness in PDT for cervical cancer.⁷⁸ Evidence suggests that methylene blue-mediated PDT successfully induces cell death in cervical cancer cells.^74,79 Upon light activation, methylene blue generates reactive oxygen species (ROS) that can damage cancer cells. In vitro and animal studies have shown the efficacy of methylene blue in killing cancer cells, but further research is needed to evaluate its effectiveness in humans.

(E) Rose Bengal: A red dye with photosensitizing properties. It has been used in medicine for many years and has also been employed in PDT for cervical cancer.⁷⁵ Upon light activation, Rose Bengal generates reactive oxygen species that can harm cancer cells. In vitro and animal studies have shown the effectiveness of Rose Bengal in killing cancer cells,⁷⁵ but further research is necessary to determine its effectiveness in humans.

(F) Zinc phthalocyanine: A photosensitizer that can be utilized in PDT for cervical cancer.⁶⁷ It exhibits high absorption in the red-light region, making it effective for PDT. When exposed to light at a specific wavelength, the photosensitizer generates reactive oxygen species capable of destroying cancer cells.⁶⁸

Table 6.

Comparison of different molecules for PDT in cervical cancer with approve preclinical effects.

Dye	Pros	Cons
Curcumin	Natural compound with low toxicityAnti-inflammatory and antioxidant propertiesHas been shown to induce cell death in cancer cellsPotential for tumor-selective accumulation	Limited water solubilityLow bioavailabilityRequires activation by light
Hypericin	High tumor selectivityGood tissue penetration	Requires activation by lightPotential skin photosensitivity
Methylene blue	FDA-approvedLow toxicity	Low tumor selectivityRequires high concentrations
Indocyanine green	FDA-approved for clinical useHigh water solubilityCan be activated by near-infrared lightAllowing for deeper tissue penetration	Limited tumor selectivityRapid clearance from the bodyMay require high doses for therapeutic effectPotential for skin photosensitivity and allergic reactions
Rose Bengal	Good tumor selectivityLow toxicity	Requires activation by lightPotential skin photosensitivity
Zinc phthalocyanine	High absorbance in the red spectrumGood tumor selectivity	Low water solubilityPotential toxicity

PDT, photodynamic therapy.

Potential molecules for PDT of cervical cancer

Several molecules have been the subject of preclinical studies for potential use in PDT for various cancers, although their application in cervical cancer settings remains unexplored.

(A) Other chlorophyll derivatives apart from chlorin e6: Chlorophyll and its derivatives have been investigated for their potential use in PDT for various cancers, including cervical cancer.⁸⁰ Studies have demonstrated that chlorophyll-based PDT can induce apoptosis in cancer cells.⁸¹

(B) Methyl violet: A cationic dye that has exhibited photodynamic activity.⁸² Preclinical studies have examined the use of methylene violet-based PDT for cancer treatment.⁸²

(C) Bacteriochlorins: Belong to a class of photosensitizers that have been investigated for their potential use in PDT for various cancers.⁸³ However, there is currently no research indicating the effectiveness of bacteriochlorin-based PDT for treating cervical cancer.

(D) Fullerenes: Carbon molecules that have been studied for their potential use in PDT for various cancers.⁸⁴ Preclinical studies have shown that fullerene-based PDT can effectively induce cell death in cancer cells.⁸⁵ Notably, preclinical studies have demonstrated that a particular fullerene, namely C60 fullerene, has shown significant promise in effectively inducing cell death in cancer cells.⁸⁶ C60 fullerene, also known as buckyball, is a specific type of fullerene with a spherical shape. Its unique structure and ability to generate reactive oxygen species upon light activation make it a promising candidate for targeted cancer therapy through PDT.⁸⁶

(E) Xanthene molecules: Xanthene molecules, such as eosin and erythrosine, are a class of fluorescent molecules used in various applications, including as photosensitizers in PDT for different cancers.⁸⁵

Challenges and solutions related to using molecules for PDT of cervical cancer

The limited solubility of molecules in water poses a significant challenge when using them for cancer treatment, as it can reduce their efficacy and increase their toxicity. However, nanotechnology offers a potential solution by enhancing the solubility, stability, and targeted delivery of molecules to cancer cells.⁸⁷

Nanoparticle-based delivery systems have been developed for various photosensitizers, including porphyrins, chlorophylls, and phycobilins. These nanoparticles can be designed to specifically target cancer cells, improve the solubility and stability of the photosensitizer, and enhance its distribution and pharmacokinetics. Moreover, some nanoparticles possess intrinsic anticancer properties and can augment the therapeutic effects of PDT.

Overall, the combination of photosensitizers and nanotechnology holds great promise for the development of effective and targeted PDT for cervical cancer and other types of cancer.

In addition to limited solubility, there are several other challenges associated with the use of molecules for PDT in cervical cancer. These challenges include:

Tumor targeting: Achieving specific targeting of the dye to tumor cells while minimizing uptake by healthy tissues is a challenge that needs to be addressed to avoid potential toxicity.⁸⁸

Depth of penetration: The depth to which the activating light can penetrate is limited, making it challenging to treat tumors located deep within the body.⁸⁹

Photobleaching: Molecules can undergo photobleaching, causing a loss of their ability to generate reactive oxygen species upon light exposure. This can limit their effectiveness in PDT.⁹⁰

Stability: Some molecules may exhibit instability in biological environments, affecting their efficacy and safety.⁹¹

Regulatory approval: Obtaining regulatory approval for clinical use can be a time-consuming and costly process, which can impede the availability of molecules for PDT in cervical cancer.⁹²

To address these challenges, potential solutions can be considered:

Solubility: Encapsulating the dye within lipid-based or polymeric nanocarriers can improve solubility and stability.⁹³

Tissue penetration: Exploring alternative delivery methods such as intratumoral injection or topical application may enhance tissue penetration.⁹⁴

Specificity: Enhancing specificity through ligand conjugation or utilizing activatable molecules that are selectively activated in cancer cells.⁶⁶

Photobleaching: Optimizing dye concentration, light dose, and using photostable molecules can help reduce photobleaching.⁹⁵

Toxicity: Mitigating toxicity by using lower dye and light doses, as well as optimizing drug delivery methods to minimize off-target effects.⁹⁶

Regulatory approval: Adhering to established regulatory guidelines for drug development and clinical trials is crucial to ensure safety and efficacy before seeking regulatory approval for clinical use.⁹⁷

Tumor targeting: Utilizing targeted delivery systems like nanoparticles, stem cell-derived exosomes, or liposomes can improve tumor targeting. These systems can be conjugated with specific ligands or antibodies that recognize and bind to tumor cells, increasing photosensitizer accumulation in the tumor while minimizing uptake in healthy tissues. Another approach involves using light sources with specific wavelengths that selectively activate the photosensitizer in tumors while minimizing activation in surrounding healthy tissues.^98–101

Limitations of this review

While our scoping review provides valuable insights into the applications of PDT for cervical cancer, it is essential to acknowledge certain limitations. Firstly, the scoping review primarily focuses on the analysis of author keywords and in silico binding affinities, which, while informative, may not fully capture the complexity of PDT applications. The identified molecules with high binding affinities, like fullerene, aluminum phthalocyanine chloride, and zinc phthalocyanine, demonstrate promise, but their clinical viability requires further validation through in vitro and in vivo studies. Furthermore, the discussion of approved molecules and ongoing clinical trials provides a comprehensive overview, but the landscape of PDT for cervical cancer may evolve with the emergence of new research. Therefore, while our review offers valuable insights, the field’s dynamic nature underscores the need for continuous exploration and validation of PDT approaches for cervical cancer treatment.

Conclusion

The findings suggest that research on PDT for cervical cancer has been ongoing for several years, although its pace may have slowed down recently. Photo chemotherapy, nanoparticles, and photosensitizing agents have emerged as commonly employed approaches in these studies. Notably, fullerene shows promise as a dye for PDT due to its strong binding affinity to overexpressed receptors in cervical cancer cells. However, further research is needed to validate Fullerene’s potential and develop effective PDT treatments for cervical cancer. The utilization of PDT, combining a fluorescent dye with a specialized imaging system, represents a significant advancement in the treatment of HPV-associated cervical lesions. This minimally invasive approach offers targeted therapy for abnormal cells while minimizing harm to healthy tissue. Furthermore, research has shown that ALA-PDT provides a safe and effective alternative for treating CIN and HSIL associated with HPV. Through early detection and treatment of these lesions, PDT and ALA-PDT have the potential to reduce the global incidence and mortality of cervical cancer. Continued research and development in this area will likely drive further progress in the treatment of HPV-related cervical lesions, leading to improved patient outcomes and a decreased global burden of cervical cancer.

Supplemental Material

sj-docx-1-taj-10.1177_20406223241233206 – Supplemental material for Photodynamic therapy of cervical cancer: a scoping review on the efficacy of various molecules

Supplemental material, sj-docx-1-taj-10.1177_20406223241233206 for Photodynamic therapy of cervical cancer: a scoping review on the efficacy of various molecules by Nasrulla Abdullaevich Shanazarov, Afshin Zare, Nadiar Maratovich Mussin, Rustam Kuanyshbekovich Albayev, Asset Askerovich Kaliyev, Yerbolat Maratovich Iztleuov, Sandugash Bakhytbekovna Smailova and Amin Tamadon in Therapeutic Advances in Chronic Disease

Supplemental Material

sj-xlsx-1-taj-10.1177_20406223241233206 – Supplemental material for Photodynamic therapy of cervical cancer: a scoping review on the efficacy of various molecules

Supplemental material, sj-xlsx-1-taj-10.1177_20406223241233206 for Photodynamic therapy of cervical cancer: a scoping review on the efficacy of various molecules by Nasrulla Abdullaevich Shanazarov, Afshin Zare, Nadiar Maratovich Mussin, Rustam Kuanyshbekovich Albayev, Asset Askerovich Kaliyev, Yerbolat Maratovich Iztleuov, Sandugash Bakhytbekovna Smailova and Amin Tamadon in Therapeutic Advances in Chronic Disease

Footnotes

Acknowledgements

None.

Declarations

ORCID iD

Amin Tamadon

Supplemental material

Supplemental material for this article is available online.

References

Arbyn

Weiderpass

Bruni

, et al. Estimates of incidence and mortality of cervical cancer in 2018: a worldwide analysis. Lancet Glob Health 2020; 8: e191–e203.

Okunade

KS.

Human papillomavirus and cervical cancer. J Obstet Gynaecol 2020; 40: 602–608.

Alrajjal

Pansare

Choudhury

MSR

, et al. Squamous intraepithelial lesions (SIL: LSIL, HSIL, ASCUS, ASC-H, LSIL-H) of uterine cervix and bethesda system. Cytojournal 2021; 18: 16.

Vanajothi

Srikanth

Vijayakumar

, et al. HPV-mediated cervical cancer: a systematic review on immunological basis, molecular biology, and immune evasion mechanisms. Curr Drug Targets 2022; 23: 782–801.

Demarco

Lorey

Fetterman

, et al. Risks of CIN 2+, CIN 3+, and cancer by cytology and human papillomavirus status: the foundation of risk-based cervical screening guidelines. J Low Genit Tract Dis 2017; 21: 261–267.

Unanyan

Pivazyan

Davydova

, et al. Efficacy of photodynamic therapy in women with HSIL, LSIL and early stage squamous cervical cancer: a systematic review and meta-analysis. Photodiagnosis Photodyn Ther 2021; 36: 102530.

Gilyadova

Ishchenko

Shiryaev

, et al. Phototheranostics of cervical neoplasms with Chlorin e6 photosensitizer. Cancers (Basel) 2022; 14: 211.

Matsui

Tamoto

Iwasa

, et al. Nonlinear optics with near-infrared excitation enable real-time quantitative diagnosis of human cervical cancers. Cancer Res 2020; 80: 3745–3754.

Feng

Tamadon

Hsueh

AJW

. Imaging the ovary. Reprod Biomed Online 2018; 36: 584–593.

10.

Yurttaş

Sevim

Çınar

, et al. The effects of zinc(II)phthalocyanine photosensitizers on biological activities of epitheloid cervix carcinoma cells and precise determination of absorbed fluence at a specific wavelength. Dyes Pigm 2022; 198: 110012.

11.

Zhang

, et al. Reactive oxygen species-based nanotherapeutics for head and neck squamous cell carcinoma. Mater Des 2022; 223: 111194.

12.

Cang

Hong

, et al. Effectiveness of photodynamic therapy with 5-aminolevulinic acid on HPV clearance in women without cervical lesions. Photodiagnosis Photodyn Ther 2021; 34: 102293.

13.

Wang

, et al. Advances in nanomaterials for the diagnosis and treatment of head and neck cancers: a review. Bioact Mater 2023; 25: 430–444.

14.

Ling

, et al. Effectiveness of photodynamic therapy in women of reproductive age with cervical high-grade squamous intraepithelial lesions (HSIL/CIN2). Photodiagnosis Photodyn Ther 2021; 36: 102517.

15.

Lan

Zhao

Liu

, et al. Photosensitizers for photodynamic therapy. Adv Healthc Mater 2019; 8: e1900132.

16.

Donthu

Kumar

Mukherjee

, et al. How to conduct a bibliometric analysis: an overview and guidelines. J Bus Res 2021; 133: 285–296.

17.

Lim

Kumar

Guidelines for interpreting the results of bibliometric analysis: a sensemaking approach. Global Bus Organizational Excellence. Epub ahead of print August 2023. DOI: 10.1002/joe.22229.

18.

Liu

Ding

Bai

, et al. Folate receptor alpha is associated with cervical carcinogenesis and regulates cervical cancer cells growth by activating ERK1/2/c-Fos/c-Jun. Biochem Biophys Res Commun 2017; 491: 1083–1091.

19.

Huang

Wei

Cheng

, et al. Iron metabolism protein transferrin receptor 1 involves in cervical cancer progression by affecting gene expression and alternative splicing in HeLa cells. Genes Genomics 2022; 44: 637–650.

20.

Souza

Martins-Cardoso

Guimaraes

, et al. Interplay between EGFR and the platelet-activating factor/PAF receptor signaling axis mediates aggressive behavior of cervical cancer. Front Oncol 2020; 10: 557280.

21.

Yoon

Kim

Jeong

, et al. CD44 receptor-mediated/reactive oxygen species-sensitive delivery of nanophotosensitizers against cervical cancer cells. Int J Mol Sci 2022; 23: 3594.

22.

Javed

Sood

Rai

, et al. ALDH1 & CD133 in invasive cervical carcinoma & their association with the outcome of chemoradiation therapy. Indian J Med Res 2021; 154: 367–374.

23.

Liu

Cai

, et al. Anti-tumour effect of in situ vaccines combined with VEGFR inhibitors in the treatment of metastatic cervical cancer. Int Immunopharmacol 2021; 101: 108302.

24.

VanHeyst

Choi

Kingsley

, et al. Ectopic tumor VCAM-1 expression in cancer metastasis and therapy resistance. Cells 2022; 11: 3922.

25.

Yang

Zhang

Zou

, et al. Synthesis and evaluation of (68)Ga-labeled dimeric cNGR peptide for PET imaging of CD13 expression with ovarian cancer xenograft. J Cancer 2021; 12: 244–252.

26.

Liu

Jin

, et al. Chlorin e6-biotin conjugates for tumor-targeting photodynamic therapy. Molecules 2021; 26: 7342.

27.

Trott

Olson

AJ.

AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J Comput Chem 2010; 31: 455–461.

28.

Kim

Chen

Cheng

, et al. PubChem 2023 update. Nucleic Acids Res 2023; 51: D1373–D1380.

29.

Kopp

Schwede

The SWISS-MODEL Repository of annotated three-dimensional protein structure homology models. Nucleic Acids Res 2004; 32: D230–D234.

30.

Chen

Zhang

, et al. 5-aminolevulinic acid-mediated photodynamic therapy effectively ameliorates HPV-infected cervical intraepithelial neoplasia. Am J Transl Res 2022; 14: 2443–2451.

31.

Zhang

Tong

, et al. Effect and rational application of topical photodynamic therapy (PDT) with 5-aminolevulinic acid (5-ALA) for treatment of cervical intraepithelial neoplasia with vaginal intraepithelial neoplasia. Photodiagnosis Photodyn Ther 2022; 37: 102634.

32.

Liu

Zheng

Chen

, et al. Comparison of the efficacy of ALA and high-frequency electric ion operating on cervical intraepithelial neoplasia grade I. Int J Clin Exp Med 2016; 9: 16782–16786.

33.

Gao

Geng

, et al. Efficacy and safety of photodynamic therapy mediated by 5-aminolevulinic acid for the treatment of cervical intraepithelial neoplasia 2: a single-center, prospective, cohort study. Photodiagnosis Photodyn Ther 2021; 36: 102472.

34.

Mizuno

Mitsui

Kajiyama

, et al. Efficacy of 5-aminolevulinic acid and LED photodynamic therapy in cervical intraepithelial neoplasia: a clinical trial. Photodiagnosis Photodyn Ther 2020; 32: 102004.

35.

Niu

Cheng

Hong

, et al. The effect of 5-aminolaevulinic acid photodynamic therapy versus CO(2) laser in the treatment of cervical low-grade squamous intraepithelial lesions with high-risk HPV infection: a non-randomized, controlled pilot study. Photodiagnosis Photodyn Ther 2021; 36: 102548.

36.

Wang

You

Zhang

, et al. Evaluation of 5-aminolevulinic acid-mediated photodynamic therapy on cervical low-grade squamous intraepithelial lesions with high-risk HPV infection. Photodiagnosis Photodyn Ther 2022; 38: 102807.

37.

Liu

, et al. Topical 5-aminolevulinic acid-mediated photodynamic therapy versus loop electrosurgical excision procedure in the treatment of cervical intraepithelial neoplasia: a retrospective study, 2012–2019. Authorea Preprints 2022. DOI: 10.22541/au.165910686.62658552/v1

38.

Inada

Buzza

Leite

MFM

, et al. Long term effectiveness of photodynamic therapy for CIN treatment. Pharmaceuticals (Basel) 2019; 12: 107.

39.

Bao

Hui

, et al. Topical photodynamic therapy with 5-aminolevulinic acid for cervical high-risk HPV infection. Photodiagnosis Photodyn Ther 2016; 13: 29–33.

40.

Barnett

Haller

Cairnduff

, et al. A randomised, double-blind, placebo-controlled trial of photodynamic therapy using 5-aminolaevulinic acid for the treatment of cervical intraepithelial neoplasia. Int J Cancer 2003; 103: 829–832.

41.

Ran

Wang

, et al. A prospective study of photodynamic therapy for cervical squamous intraepithelial lesion. Photodiagnosis Photodyn Ther 2021; 34: 102185.

42.

Cai

Che

Sun

, et al. Clinical outcome of photodynamic therapy for the treatment of cervical intraepithelial neoplasia grade 2. Photodiagnosis Photodyn Ther 2022; 39: 102906.

43.

Maldonado Alvarado

Osorio Peralta

Moreno Vazquez

, et al. Effectiveness of photodynamic therapy in elimination of HPV-16 and HPV-18 associated with CIN I in Mexican women. Photochem Photobiol 2017; 93: 1269–1275.

44.

Vendette

ACF

Piva

Muehlmann

, et al. Clinical treatment of intra-epithelia cervical neoplasia with photodynamic therapy. Int J Hyperthermia 2020; 37: 50–58.

45.

Yao

Yan

Zhou

, et al. A chlorin e6 derivative-mediated photodynamic therapy for patients with cervical and vaginal low-grade squamous intraepithelial lesions: a retrospective analysis. Translational Biophotonics 2022; 5: e202200006.

46.

Afanasiev

Dushkin

Grishacheva

, et al. Photodynamic therapy for early-stage cervical cancer treatment. Photodiagnosis Photodyn Ther 2022; 37: 102620.

47.

Hillemanns

Garcia

Petry

, et al. A randomized study of hexaminolevulinate photodynamic therapy in patients with cervical intraepithelial neoplasia 1/2. Am J Obstet Gynecol 2015; 212: 465 e1–465 e7.

48.

Yamaguchi

Tsuda

Takemori

, et al. Photodynamic therapy for cervical intraepithelial neoplasia. Oncology 2005; 69: 110–116.

49.

Nakamura

Oinuma

Usefulness of photodynamic diagnosis and therapy using talaporfin sodium for an advanced-aged patient with inoperable gastric cancer (a secondary publication). Laser Ther 2014; 23: 201–210.

50.

Zhang

Tang

, et al. The effect of high-risk HPV E6/E7 mRNA on the efficacy of topical photodynamic therapy with 5-aminolevulinic acid for cervical high-grade squamous intraepithelial lesions. Photodiagnosis Photodyn Ther 2022; 39: 102974.

51.

Keefe

Tadir

Tromberg

, et al. Photodynamic therapy of high-grade cervical intraepithelial neoplasia with 5-aminolevulinic acid. Lasers Surg Med 2002; 31: 289–293.

52.

Hillemanns

Korell

Schmitt-Sody

, et al. Photodynamic therapy in women with cervical intraepithelial neoplasia using topically applied 5-aminolevulinic acid. Int J Cancer 1999; 81: 34–38.

53.

Wang

Chen

, et al. Successful photodynamic therapy with topical 5-aminolevulinic acid for five cases of cervical intraepithelial neoplasia. Arch Gynecol Obstet 2010; 282: 307–312.

54.

Wang

Liu

Zhang

, et al. Evaluation of the efficacy and safety of 5-aminolevulinic acid-mediated photodynamic therapy in women with high-risk HPV persistent infection after cervical conization. Photodiagnosis Photodyn Ther 2022; 40: 103144.

55.

Wang

Zhang

, et al. The effect of local photodynamic therapy with 5-aminolevulinic acid in treating different grades of cervical intraepithelial neoplasia. Photodiagnosis Photodyn Ther 2022; 40: 103196.

56.

Wang

Qiu

, et al. Efficacy of photodynamic therapy with 5-aminolevulinic acid for the treatment of cervical high-grade squamous intraepithelial lesions with high-risk HPV infection: a retrospective study. Photodiagnosis Photodyn Ther 2022; 40: 103068.

57.

Tang

, et al. Therapeutic effects of topical photodynamic therapy with 5-aminolevulinic acid on cervical high-grade squamous intraepithelial lesions. Photodiagnosis Photodyn Ther 2022; 39: 102884.

58.

Park

CH.

Clinical efficacy of photodynamic therapy. Obstet Gynecol Sci 2016; 59: 479–488.

59.

Istomin

Lapzevich

Chalau

, et al. Photodynamic therapy of cervical intraepithelial neoplasia grades II and III with Photolon. Photodiagnosis Photodyn Ther 2010; 7: 144–151.

60.

Choi

Jung

Park

, et al. Photodynamic therapy for management of cervical intraepithelial neoplasia II and III in young patients and obstetric outcomes. Lasers Surg Med 2013; 45: 564–572.

61.

Kim

Choi

Lee

, et al. Long-term outcomes of photodynamic therapy for a positive resection margin after conization for cervical intraepithelial neoplasia grade 3. Photodiagnosis Photodyn Ther 2022; 37: 102639.

62.

Trushina

Novikova

Sokolov

, et al. Photodynamic therapy of virus-associated precancer and early stages cancer of cervix uteri. Photodiagnosis Photodyn Ther 2008; 5: 256–259.

63.

Ichimura

Yamaguchi

Kojima

, et al. Eradication and reinfection of human papillomavirus after photodynamic therapy for cervical intraepithelial neoplasia. Int J Clin Oncol 2003; 8: 322–325.

64.

Soergel

Wang

Stepp

, et al. Photodynamic therapy of cervical intraepithelial neoplasia with hexaminolevulinate. Lasers Surg Med 2008; 40: 611–615.

65.

Guo

Sun

Jiang

, et al. Recent developments of nanoparticles in the treatment of photodynamic therapy for cervical cancer. Anticancer Agents Med Chem 2019; 19: 1809–1819.

66.

Gierlich

Mata

Donohoe

, et al. Ligand-targeted delivery of photosensitizers for cancer treatment. Molecules 2020; 25: 5317.

67.

Zhang

Tang

, et al. Comparative study of topical 5-aminolevulinic acid photodynamic therapy (5-ALA-PDT) and surgery for the treatment of high-grade vaginal intraepithelial neoplasia. Photodiagnosis Photodyn Ther 2022; 39: 102958.

68.

Hodgkinson

Kruger

Mokwena

, et al. Cervical cancer cells (HeLa) response to photodynamic therapy using a zinc phthalocyanine photosensitizer. J Photochem Photobiol B 2017; 177: 32–38.

69.

Gallegos

DeLeon Rodriguez

Martinez Guzman

, et al. In vitro study of biosynthesis of protoporphyrin IX induced by delta-aminolevulinic acid in normal and cancerous cells of the human cervix. Arch Med Res 1999; 30: 163–170.

70.

Rosenthal

Nurenberg

Becerra

, et al. A phase I single-dose trial of gadolinium texaphyrin (Gd-Tex), a tumor selective radiation sensitizer detectable by magnetic resonance imaging. Clin Cancer Res 1999; 5: 739–745.

71.

Cheng

MHY

Overchuk

Rajora

, et al. Targeted Theranostic (111)In/Lu-Nanotexaphyrin for SPECT imaging and photodynamic therapy. Mol Pharm 2021; 19: 1803–1813.

72.

de Matos

RPA

Calmon

Amantino

, et al. Biomed Res Int 2018; 2018: 4057959.

73.

Yuan

, et al. Effects of notch signaling pathway in cervical cancer by curcumin mediated photodynamic therapy and its possible mechanisms in vitro and in vivo. J Cancer 2019; 10: 4114–4122.

74.

Jiao

Chen

, et al. Methylene blue-mediated photodynamic therapy induces mitochondria-dependent apoptosis in HeLa cell. J Cell Biochem 2008; 105: 1451–1460.

75.

Chan

BCL

Dharmaratne

Wang

, et al. Hypericin and pheophorbide a mediated photodynamic therapy fighting MRSA wound infections: a translational study from in vitro to in vivo. Pharmaceutics 2021; 13: 1399.

76.

Fan

Chen

, et al. New indocyanine green therapeutic fluorescence nanoprobes assisted high-efficient photothermal therapy for cervical cancer. Dyes Pigm 2022; 200: 110174.

77.

Ghorbani

Attaran-Kakhki

Sazgarnia

The synergistic effect of photodynamic therapy and photothermal therapy in the presence of gold-gold sulfide nanoshells conjugated Indocyanine green on HeLa cells. Photodiagnosis Photodyn Ther 2017; 17: 48–55.

78.

Lim

DJ.

Methylene blue-based nano and microparticles: fabrication and applications in photodynamic therapy. Polymers (Basel) 2021; 13: 3955.

79.

Hsu

Huang

, et al. Development of therapeutic Au-methylene blue nanoparticles for targeted photodynamic therapy of cervical cancer cells. ACS Appl Mater Interfaces 2015; 7: 432–441.

80.

Chaturvedi

Kim

, et al. Phototoxic effects of pyropheophorbide-a from chlorophyll-a on cervical cancer cells. J Porphyrins Phthalocyanines 2014; 18: 182–187.

81.

Alam

Minocha

Yadav

, et al. Therapeutic potential of chlorophyll functionalized carbon quantum dots against cervical cancer. Chemistryselect 2022; 7: e202204562.

82.

Kiriyanthan

Sharmili

Balaji

, et al. Photocatalytic, antiproliferative and antimicrobial properties of copper nanoparticles synthesized using Manilkara zapota leaf extract: a photodynamic approach. Photodiagnosis Photodyn Ther 2020; 32: 102058.

83.

Huang

Balasubramanian

Yang

, et al. Stable synthetic bacteriochlorins for photodynamic therapy: role of dicyano peripheral groups, central metal substitution (2H, Zn, Pd), and Cremophor EL delivery. ChemMedChem 2012; 7: 2155–2167.

84.

Huang

Sharma

Yin

, et al. Functionalized fullerenes in photodynamic therapy. J Biomed Nanotechnol 2014; 10: 1918–1936.

85.

Otake

Sakuma

Torii

, et al. Effect and mechanism of a new photodynamic therapy with glycoconjugated fullerene. Photochem Photobiol 2010; 86: 1356–1363.

86.

Fernandes

Shenoy

RUK

Kajampady

, et al. Fullerenes for the treatment of cancer: an emerging tool. Environ Sci Pollut Res Int 2022; 29: 58607–58627.

87.

Baghban

Khoradmehr

Nabipour

, et al. The potential of marine-based gold nanomaterials in cancer therapy: a mini-review. Gold Bulletin 2022; 55: 53–63.

88.

Hong

Choi

Shim

MS.

Targeted and effective photodynamic therapy for cancer using functionalized nanomaterials. Acta Pharm Sin B 2016; 6: 297–307.

89.

Gunaydin

Gedik

Ayan

Photodynamic therapy-current limitations and novel approaches. Front Chem 2021; 9: 691697.

90.

Abrahamse

Hamblin

MR.

New photosensitizers for photodynamic therapy. Biochem J 2016; 473: 347–364.

91.

Dereje

Pontremoli

Moran Plata

, et al. Polymethine dyes for PDT: recent advances and perspectives to drive future applications. Photochem Photobiol Sci 2022; 21: 397–419.

92.

van Straten

Mashayekhi

de Bruijn

, et al. Oncologic photodynamic therapy: basic principles, current clinical status and future directions. Cancers (Basel) 2017; 9: 19.

93.

Huh

KM.

Polymeric nanocarrier systems for photodynamic therapy. Biomater Res 2014; 18: 19.

94.

Huang

Meyers

, et al. Photodynamic therapy for treatment of solid tumors–potential and technical challenges. Technol Cancer Res Treat 2008; 7: 309–320.

95.

Tasso

Schlothauer

Junqueira

, et al. Photobleaching efficiency parallels the enhancement of membrane damage for porphyrazine photosensitizers. J Am Chem Soc 2019; 141: 15547–15556.

96.

Algorri

Lopez-Higuera

Rodriguez-Cobo

, et al. Advanced light source technologies for photodynamic therapy of skin cancer lesions. Pharmaceutics 2023; 15: 2075.

97.

Selker

Eichler

Stockbridge

, et al. Efficacy and effectiveness too trials: clinical trial designs to generate evidence on efficacy and on effectiveness in wide practice. Clin Pharmacol Ther 2019; 105: 857–866.

98.

Baghban

Khoradmehr

Afshar

, et al. MRI tracking of marine proliferating cells in vivo using anti-Oct4 antibody-conjugated iron nanoparticles for precision in regenerative medicine. Biosensors (Basel) 2023; 13: 268.

99.

Afshar

Zare

Farrar

, et al. Exosomes of mesenchymal stem cells as nano-cargos for anti-SARS-CoV-2 asRNAs. Mod Med Lab J 2021; 4: 11–18.

100.

Salehpour

Balmagambetova

Mussin

, et al. Mesenchymal stromal/stem cell-derived exosomes and genitourinary cancers: a mini review. Front Cell Dev Biol 2022; 10: 1115786.

101.

Nowzari

Wang

Khoradmehr

, et al. Three-dimensional imaging in stem cell-based researches. Front Vet Sci 2021; 8: 657525.

Supplementary Material

Please find the following supplemental material available below.

For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.

For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.

0.00 MB

0.24 MB

0.38 MB