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Abstract

Chemokine ligand 11 is a member of the CXC chemokine family and exerts its biological function mainly through binding to CXCR3 and CXCR7. The CXCL11 gene is ubiquitously overexpressed in various human malignant tumors; however, its specific mechanisms vary among different cancer types. Recent studies have found that CXCL11 is involved in the activation of multiple oncogenic signaling pathways and is closely related to tumorigenesis, progression, chemotherapy tolerance, immunotherapy efficacy, and poor prognosis. Depending on the specific expression of its receptor subtype, CXCL11 also has a complex 2-fold role in tumours; therefore, directly targeting the structure-function of CXCL11 and its receptors may be a challenging task. In this review, we summarize the biological functions of CXCL11 and its receptors and their roles in various types of malignant tumors and point out the directions for clinical applications.

Plain language summary

CXCL11 is found in many types of cancer and affects how cancer cells grow and respond to treatments. This paper delves into the intricate dance between CXCL11 and its receptors in various types of cancer. Like a versatile actor playing different roles on stage, CXCL11 can either promote or hinder cancer growth depending on its interaction with specific receptors. Understanding how CXCL11 works could help develop new treatments for cancer, but it's a complex challenge because CXCL11 can have different effects depending on the type of cancer and which receptors it binds to.

Keywords

CXCL11 malignant tumor chemokine chemokine receptor targeted therapy

Introduction

With changes in global demographic characteristics and lifestyles, the risk of malignant tumors is increasingly becoming a serious burden on the lives and economies of people in all countries. According to estimates by the World Health Organization, in 2019, cancer was the leading or second leading cause of death in 183 countries worldwide.¹ And according to projections, these burdens are still expected to continue to increase, with 22 million new cancer cases and associated deaths with 13 million cancers expected by 2030.² A recent study found that CXCL11 of the chemokine family is significantly more expressed in most types of malignant tissues than in non-tumour tissues.³

Unlike the earliest beliefs that it only participates in the intrinsic inflammatory response or functions as an immunosurveillance mediator, CXCL11 not only regulates the directional movement of cancer cells but also participates in the entry and exit of cancer cells into and out of blood vessels, immune evasion, proliferation, and angiogenesis.⁴ Meanwhile, CXCL11 exhibits two sides in tumor development depending on the different receptors or receptor subtypes to which it binds; thus, chemokines are not only confounding with their receptors (multiple chemokines can share the same receptor), but also the same ligand itself is pleiotropic (binds to different receptors or receptor subtypes and thus mediates different effects), which poses an even greater challenge for its clinical application.

It is currently believed that CXCL11 overexpression in a variety of human malignant tumors leads to an imbalance between cell proliferation and apoptosis, and in particular, its effects on immune cells are involved in a variety of tumorigenesis and developmental processes. Although current studies have made some progress, the main mechanism of action of CXCL11 on malignant tumors of different tissue types is not the same. We have conducted a comprehensive review of CXCL11 and its receptors with a focus on their biological functions, relevance in various malignancies (Table 1), and clinical value.

Table 1.

Role of CXCL11 and its Receptors in Human Malignancies.

Tumour type	Ligand - Receptors	Meaning	Mechanism of action	Results	Ref.
COADREAD	CXCL11	Tumor promotor	Colon cancer cells overexpressing RBP-Jκ induce the expression of TGF-β1 in TAMs through the secretion of CXCL11, enhancing the infiltration of TAMs into the tumor environment	Promotes EMT of cancer and facilitates tumor metastasis	^5,6
	CXCL11–CXCR3	Associates with tumor	CXCR3-A and CXCR3-B have antagonistic effects on each other, with CXCR3-B being more expressed in non-tumor tissues	Elevated expression of CXCR3-A signifies a poor prognosis, whereas CXCR3-B suggests the opposite	⁷
STAD	CXCL11–CXCR3	Tumour inhibitor	CXCL11 activates CXCR3 in GC cells, upregulating PD-L1 expression through STAT and PI3K-Akt pathways	Enhancing the effectiveness of immunotherapy	⁸
		Tumour inhibitor	Mediates the infiltration of cytotoxic T lymphocytes and inhibits angiogenesis, which can be inhibited by H. pylori	Inhibition of tumor growth	^9,10
	CXCL11	Tumour inhibitor	Activates Th1 and promotes M1 polarization in macrophages	Inhibition of tumor growth	¹¹
HCC	CXCL11–CXCR3	Tumor promotor	α2δ1⁺ HCC TIC promotes tumor stem cells through a self-secretory pathway, activating the ERK1/2 pathway	Promotes tumor self-renewal and chemotherapy resistance	¹²
	CXCL11	Tumor promotor	Promotes HCC cell proliferation and migration through the LINC00152/miR-205-5p/CXCL11 axis	Promotes tumor growth and metastasis	¹³
			Promotes HCC cell migration through the circUBAP2/miR4756/IFIT1/3 axis	Promotes tumor metastasis	¹³
		Associates with tumor	Elevated expression in viral hepatitis and liver cirrhosis	Elevated with the progression of liver inflammation or fibrosis	^14-16
BLCA	CXCL11-CXCR3	Tumour inhibitor	Highly active CD8 ⁺ cells in the tumor microenvironment express more CXCR3-alt	Improvement in chemotherapy sensitivity	¹⁷
	CXCL11	Tumour inhibitor	BCG treatment enhances the presentation of BCG-cancer cell conjugates to antitumor immune cells	Inhibition of tumor growth	¹⁸
RC	CXCL11	Tumor promotor	EP300/CBP modifies and enhances the expression of RBM15, stabilizes the level of CXCL11 mRNA, and ultimately leads to M2 polarization of macrophages	Promotes tumor proliferation and migration	¹⁹
	CXCL11-CXCR3	Tumor promotor	Highly expressed in the tumor vasculature	Promotes tumor angiogenesis	²⁰
	CXCL11-CXCR3	Tumour inhibitor	CXCR3-B has immunosuppressive tumor vasculature activity	Inhibition of tumor angiogenesis	²¹
LUNG	CXCL11-CXCR3	Tumour inhibitor	CXCL11-CXCR3 induces infiltration of CD8 ⁺ T cells and suppresses angiogenesis	Augmenting the efficacy of immunotherapy	²²
	CXCL11	Tumour inhibitor	DOC upregulates the secretion of HMGB1/NF-Κb/CXCL11 via the ROS pathway, resulting in increased infiltration of CD8 ⁺ T cells	Enhances chemotherapy sensitivity	²³
		Tumor inhibitor	Knocking out the RUNX3 gene leads to downregulation of CXCL11 mRNA expression and increases osteoclast activity	Counteracts the osteolytic activity of tumor cells	²⁴
HNSCC	CXCL11-CXR3	Tumor promotor	Tumorinflamed LEC overexpress MMP7 and activate the JAK-STAT and AKT pathways, inducing tumor cell EMT	Promotes lymph node metastasis of tumors	²⁵
OC	CXCL11-CXCR3	Tumor promotor	Markedly elevated OC expression, promoting intracellular D274 and IDO1 expression	Promotes tumor growth and immune escape	²⁶
			Significantly elevated expression in oral mucosal leukoplakia	Promotion of precancerous lesions
	CXCL11-CXCR7	Tumor promotor	Expression gradually increases in premalignant oral lesions and advanced-stage oral cancer	Promotes early malignant transformation and tumor development	²⁷
SKCM	CXCL11	Associates with tumor	Associations with immune infiltration and inverse correlation with prognosis	Suggests poor prognosis (Bioinformatics analysis)	^28,29
	CXCL11-CXCR3	Tumor promotor	Induces cellular cytoskeletal remodeling	Promotes tumor metastasis	³⁰
	CXCL11	Tumor Inhibitor	Recruits immune cells, promotes marrow activation, and enhances antitumor immune responses	Inhibition of tumor growth	³¹
BC	CXCL11	Tumor Inhibitor	The IFI16-STING pathway promotes CD8 ⁺ T cell infiltration and enhances memory T cell abundance	Influence on the efficacy of targeted therapy	³²
		Associates with tumor	Serum CXCL11 levels are lower in HR⁺ breast cancer patients compared to HR^- patients	Predicts treatment efficacy	³³
		Associates with tumor	Expression levels of I-TAC are downregulated in tissue and negatively correlate with staging of BC	Suggests tumor progression	³⁴
	CXCL11-CXCR3	Tumor promotor	Aged endothelial cells release through the chemokine receptor axis, activating the ERK pathway	Enhances tumor invasion	³⁵
MM	CXCL11	Tumor promotor	Activates tyrosine kinase, inducing secretion of MMP-2 and MMP-9	Promotes tumor growth and metastasis	³⁶
	CXCL11-CXCR3	Tumor inhibitor	Chemotaxis attracts immunoreactive cells	Inhibition of tumor growth
CLL	CXCL11	Associates with tumor	GHV mutation significantly correlates with CXCL11	Predicts prognosis	³⁷
DLBCL	CXCL11	Associates with tumor	Expresses higher levels in advanced-stage tumours; associates with tumor diagnosis	Diagnostic support; Assess the extent of tumor progression	³⁸
OV	CXCL11-CXCR7	Tumor promotor	ERα enhances the expression of the CXCL11–CXCR7 axis, promoting tumor cell EMT through a feedforward regulatory mechanism	Promotes tumor metastasis	³⁹
	CXCL11-CXCR3	Tumor promotor	High expression of CXCR3-A in endometriosis inhibits cytotoxic T cells	Promotion of precancerous lesions	^40,41
PAAD	CXCL11	Associations with tumor development	Elevated serum CXCL11 levels in patients	Diagnostic support	⁴²
PRAD	CXCL11	Associates with tumor	Elevated serum CXCL11 levels in patients	Diagnostic support	⁴³
BCC	CXCL11-CXCR3	Tumor promotor	Promotes the proliferation of human immortalized keratinocytes	Promotes tumor growth	⁴⁴
THCA	CXCL11-CXCR7	Tumor promotor	Promotes angiogenesis in metastatic THCA through an EGF-EGFR positive feedback loop	Promotes tumor angiogenesis	⁴⁵
	CXCL11	Tumor inhibitor	Induction of CXCL11 release by IFN-γ or PPARγ agonists inhibits endothelial cell proliferation, suppresses basal cell migration, and induces apoptosis	Inhibition of tumor growth and migration	⁴⁶

Carcinoma abbreviations: COADREAD: colon adenocarcinoma and rectal adenocarcinoma, STAD: stomach adenocarcinoma, HCC: hepatocellular carcinoma, BLCA: bladder urothelial carcinoma, RC: renal carcinoma, LUNG: lung cancer, HNSCC: head and neck squamous cell carcinoma, OC: oral cancer, SKCM: skin cutaneous melanomas, BC: breast cancer, MM: multiple myeloma, CLL: chronic lymphocytic leukemia, DLBCL: diffuse large B-cell lymphoma, OV: ovarian cancer, PAAD: pancreatic adenocarcinoma, PRAD: prostate adenocarcinoma, BCC: basal cell carcinoma, THCA: thyroid carcinoma.

Composition and Role of the Chemokine Family

Chemokines refer to a group of small-molecule proteins that are secreted. To date, over 50 chemokines and 20 chemokine receptors have been characterized. These chemokines are categorized into four distinct subfamilies, namely CC, CXC, CX₃C, and XC, based on the specific configuration of their two N-terminal cysteine residues.^47,48 They mediate signaling events through seven-transmembrane structures, specifically G protein-coupled receptors (GPCRs), which are on the cellular surface. These receptors, known as chemokine receptors, have extracellular and cytoplasmic N termini. Their interaction with chemokine ligands initiates the activation of the G protein-coupled receptor (GPCR) signaling pathway. This activation typically starts with the disassociation of classical G protein subunits, specifically Gα, Gβ, and Gγ. Subsequently, this cascade eventuates in the generation of a secondary messenger, which in turn activates various effector enzymes (Figure 1). This intricate series of intracellular events encompasses calcium efflux and culminates in the orchestration of many biological effects.⁴⁹ Chemokine receptors are commonly expressed on tumor cells, vascular endothelial cells and leukocytes, which also secrete some chemokine ligands by autocrine or paracrine means. As a class of structurally related small molecules, they are approximately 20%–50% identical, meaning that they share genetic and amino acid sequences. Chemokines assist in this process called “chemotaxis” by regulating the transport of various types of leukocytes ,⁴⁸ allowing cells to NF-κB rate to the source of the chemokine along with signals of increased chemokine concentration when the body is clearing invading pathogens or performing autoimmunity. However, the functions of chemokines in the growth and spread of a variety of tumors have also been confirmed in recent studies ,^50,51and they are also closely associated with tumor chemoresistance and poor prognosis. These qualities have made chemokines increasingly the focus of clinical therapy, and understanding their mechanisms of action may lead to new therapies for various human malignancies.

Figure 1.

Receptors for CXCL11 act through multiple signaling pathways. (1). Typical chemokine receptors, such as CXCR3, function as G-protein-coupled receptors and exert their biological effects through multiple downstream signaling pathways. (2). CXCR7 was previously thought to be incapable of activating typical G-protein signaling pathways. However, recent studies have found that it can activate ERK through the β-arrestin pathway. The figure was partly generated using Servier Medical Art, provided by Servier, licensed under a Creative Commons Attribution 3.0 unported license. GTP, guanosine triphosphate; GDP, guanosine diphosphate; ATP, adenosine triphosphate; cAMP, cyclic adenosine monophosphate.

Structure and Biological Function of CXCL11 and its Receptor

CXCL11

The gene encoding C-X-C Motif Chemokine Ligand 11 is located on human chromosome 4q21.2 and contains four exons and at least three polyadenylation signals, IFN-γ, IFN-α and IFN-β are effective inducers of transcription of the gene, but the induction of IFN-α is relatively weak; therefore, CXCL11 is also known as an IFN-inducible T-cell α-chemoattractant. In the human body, it is secreted mainly by monocytes, endothelial cells, fibroblasts, and cancer cells in response to IFNs. The CXC chemokine family is subdivided into two subfamilies based on the presence or absence of the Glu-Leu-Arg (ELR) amino acid sequence before the first cysteine residue. In general, ELR + chemokines preferentially attract neutrophils and act as pro-angiogenic, whereas ELR chemokines act on lymphocytes but are vaso-inhibitory.^50,52 Meanwhile, CXCL11 belongs to the latter.⁵³ The CXCL11 protein comprises 94 amino acids and has a molecular weight of approximately 10,365 Da. It has a typical chemokine sheeting structure, as determined by an NMR spectroscopy study, with a three-stranded antiparallel β-sheet opposite an α-helix, a long N-terminal end stabilized by two disulfide bonds, and a 310-helix just at the N-terminal end of the first β-sheet.⁵⁴ The classical receptor for CXC11 is predominantly CXCR3, and it also has the strongest affinity of the multiple chemokines that share this receptor. It has recently been shown to bind to another chemokine receptor, CXCR7. Given the undeniable role of CXCL11 in modulating the body’s immune response, extensive evaluations have been conducted regarding the potential of targeting CXCL11 in cancer immunotherapy. Immune checkpoint inhibitors (ICIs) play a crucial role in this context (Table 2). However, the role of CXCL11 in neoplastic diseases cannot yet be generalized, and although there is a large body of evidence that CXCL11 is associated with the development of a variety of tumours, some studies have demonstrated that CXCL11 can bind to some proteins to exert anti-tumour effects,⁶⁰ which makes it necessary to maintain a more cautious approach when intending to use it as a target for targeted tumour therapy. We will elaborate on its relationship with malignant diseases in subsequent chapters.

Table 2.

Associations Between ICIs and CXCL11 in Cancer Immunotherapy.

Tumor Type	Association	ref
Gastric cancer	1. The CXCL11–CXCR3 axis may upregulate the expression of PD-L1 in gastric cancer (GC) cells through the activation of STAT and PI3K– Akt signaling pathways	⁸
Gastric cancer	2. A significant positive correlation was observed between the expression levels of PD-L1 and CXCR3 in gastric cancer tissues	⁸
Lung cancer	1. Silencing CXCL11 and CXCR3 in tumor cells can suppress the antitumor and antiangiogenic effects of PD-L1 inhibitors. Upregulation of IFN-γ-stimulated CXCL11 expression is associated with sensitivity to PD-L1 receptor blockade	^22,55
Lung cancer	2. Early elevation of peripheral blood levels of CXCL11 and IFN-γ may serve as indicators of increased immune-related adverse events	^22,55
Head and neck squamous cell carcinoma	1. The low expression of the immune-related lncRNA TRG-AS1 can induce the expression of CXCL11 in the tumor microenvironment and serve as a novel biomarker for predicting the efficacy of PD-1 treatment	^56,57
Head and neck squamous cell carcinoma	2. Patients with a history of smoking exhibit a lower number of PD-1+-positive cells, possibly because of a weakened ability of CXCL11 to recruit cytotoxic T cells and NK cells	^56,57
Oral leukoplakia (precancerous lesions)	Knocking down CXCL11 inhibits the expression of intracellular immune checkpoints, primarily CD274 and IDO1	²⁶
Skin melanoma	1. Early elevation of peripheral blood levels of CXCL11 and IFN-γ may serve as indicators of increased immune-related adverse events	^22,58
Skin melanoma	2. Tumor microenvironments rich in CD16 ⁺ macrophages can enhance the response to combined immune therapy targeting PD-1 and CTLA-4. Upregulation of CXCL11 gene expression is observed in this context	^22,58
Breast cancer	1. Exercise training can enhance CD8 ⁺ T cell infiltration in breast cancer, making it more responsive to ICI treatment through the CXCL11-CXCR3 signaling pathway	⁵⁹

CXCR3

The gene encoding CXCR3 is located on human X chromosome q13.1.⁶¹ In tumourous tumorous, CXCR3 and its ligands are expressed on tumor cells, stromal cells, blood vessels and recruited leukocytes.⁶² CXCR3 has at least three variable splicesomes: CXCR3A,CXCR3B, and CXCR3-alt,⁶³ with CXCL11 having higher affinity potency for CACR3-A. CXCRA/B has opposing roles in tumor function due to mediating different signaling cascade pathways or affinity for different cell types.^64,65 Usually, CXCR3-A, which is mainly expressed in T lymphocytes and NK cells,⁶⁶ transmits signals that promote cell proliferation and chemotaxis. CXCR3-B, which is mainly expressed in fibroblasts, endothelial cells, and epithelial cells, mainly inhibits cell proliferation and migration and induces apoptosis. CXCR3-B has a high structural similarity to CXCR3-A, which contains a longer NH2-terminal extracellular domain,⁶⁷ but the rest of the structure is highly overlapping.CXCR3-alt has a very different structure, which contains a truncated C-terminus and only four transmembrane helices, and has been found to bind only to CXCL11,^63,68 and as with its most recent discovery, its function has not yet been thoroughly investigated. CXCL11 interacts with its receptor CXCR3 at two successive sites in its structure,^69,70 with the receptor first being recognized and bound by the N-loop region of the protein, followed by activation of the CXCR3 receptor by the flexible N-terminal region of the chemokine, which presents a “two-step” mode of action .⁵⁴ The two main variants mediating CXCR3 may be expressed in the tumor microenvironment; therefore, it cannot be simply asserted that CXCR3 is an oncogenic or a manostatic factor (Figure 2).

Figure 2.

Role of the CXCL11–CXCR3 axis in the tumor microenvironment. (A): CXCR3 composition. According to the difference in the fragment of the amino terminus of the receptor protein, CXCR3 can be classified into three isoforms: CXCR3-A, CXCR3-B, and the truncated variant CXCR3-alt. CXCR3A promotes the proliferation and migration of cancer cells, whereas CXCR3B inhibits the proliferation and migration of cells, and the function of CXCR3-alt has not yet been fully clarified. (B&C): CXCL11-CXCR3 axis: The CXCL11–CXCR3 axis acts in two main directions: the direction of paracrine signaling for the promotion of immune responses and the direction of autocrine signaling for the proliferation and metastasis of cancer cells. (B): Paracrine secretion of CXCR3. Mediated by IFNs, CXCL 11 is secreted mainly by monocytes, endothelial cells, fibroblasts, and cancer cells. The main function of this axis is to stimulate the migration, differentiation, and activation of immune cells. It acts as a tumor suppressor by recruiting CTL, NK cells and macrophages. Simultaneously secreted CXCL11 recruits CD8⁺ CTLs to local tissues, and IFN-γ produced by CD8⁺ CTLs further stimulate tissue cells to produce more CXCL11. Increased release of chemokines and enhanced inflammatory response leads to further accumulation of anti-tumor immune cells expressing CXCR3, forming a tumor-suppressive microenvironment. (C): Autocrine secretion of CXCR3. In the direction of autocrine signaling, CXCR3 (mainly CXCR3A) can make cancer cells susceptible and further grow and metastasize. Tumour-derived CXCL11 is also responsible for the recruitment of Th cells, Tregs, and MDSCs, which play a role in creating a tumour-friendly microenvironment. The figure was partly generated using Servier Medical Art, provided by Servier, licensed under a Creative Commons Attribution 3.0 unported license. CTL, cytotoxic lymphocytes; NK, natural killer cells; Th1, T help1; Th2, T help2; Tregs, regulatory T cells; MDSC, myeloid-derived suppressor cells.

CXCR7

CXCR7 was first cloned from a dog thyroid cDNA library by Liber et al. in 1989.⁷¹ However, its biological function was not thoroughly understood for a long time. Initially, it was believed to be the receptor for vasoactive intestinal peptide,^72,73 but this hypothesis was not supported by subsequent research. Until 2005, CXCR7 was found to be a high-affinity receptor for CXCL12.⁷⁴ Prior to this, CXCL12 was thought to only interact with CXCR4. Subsequently, Burns demonstrated that CXCR7 also has a certain affinity for CXCL11.⁷⁵ The human CXCR7 gene is at position 2q37.3 on the chromosome and contains 7 exons, but only the last exon is responsible for translation.⁷⁶ Unlike other classical chemokine receptors, CXCR7 has been shown to not induce calcium flux in various cell lines; hence, it may not signal through the traditional G protein-mediated pathway. Currently, one possible mechanism by which CXCR7 exerts its effects is through the β-arrestin pathway.⁷⁷ It has also been renamed as atypical chemokine receptor 3 (ACKR3) by the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology.⁷⁸ In multiple malignant tumor diseases, CXCR7 has been found to be associated with cancer cell growth, metastasis, or angiogenesis, such as colorectal cancer,⁷⁹ breast cancer,⁸⁰ prostate cancer,⁸¹ melanoma,⁸² etc.

Role of CXCL11 in Human Malignant Tumors

CXCL11 in Colon Adenocarcinoma and Rectal Adenocarcinoma (COADREAD)

RBP-Jκ is a protein that can bind to a DNA fragment carrying the immunoglobulin Jκ recombination signal sequence. In addition, it plays a pivotal role as a core factor in the classical Notch signaling pathway.⁸³ Overexpression of RBP-Jκ in colorectal cancer can lead to the secretion of CXCL11 by cancer cells, enhancing the metastatic potential of colorectal cancer. CXCL11 can induce a high degree of infiltration of tumor-associated macrophages (TAMs) in colorectal tumors and stimulate these macrophages to secrete TGF-β1. This ultimately promotes the epithelial– mesenchymal transition (EMT), migration, and invasion of colorectal cancer cells.⁵ Neuroendocrine differentiation in colorectal cancer is a significant factor leading to poor prognosis in patients. Studies have shown that CXCL11 is also a key chemokine in neuroendocrine-like cells. Similarly, it can recruit tumorassociated macrophages to infiltrate tumor tissues, leading to more malignant biological behavior.⁶ Similarly, as with its role in other parts of the tumor, the receptor of CXCL11, CXCR3, exhibits a dual role of tumor suppression or promotion in colorectal cancer because of its different splice variants. Rupertus found that colorectal cancer cells locally exposed to CXCL11 significantly increased their invasiveness, but there was no obvious angiogenic effect. Furthermore, if the blockage of CXL11 and CXCL12 is combined, a decrease in tumor growth and invasive growth characteristics of the tumor can be observed.⁸⁴ Moreover, due to the independent regulatory role of CXCL12 on tumor angiogenesis mediated by CXCR7,⁸⁵ it is possible that the CXCL11–CXCR7 axis plays a significant role in the angiogenesis of colorectal tumors rather than the CXCL11–CXCR3 axis. Given the potential for competitive expression between CXCR3-B and CXCR3-A, the interplay within the CXCL11–CXCR3 axis in colorectal cancer and its implications for tumor progression in patients are rendered more intricate. Presently, research has revealed a marked upregulation of CXCR3-A within tumor tissues as compared to their adjacent counterparts, whereas CXCR3-B exhibits a contrasting pattern of expression.⁷ Concurrently, analyses have indicated that upregulation of CXCL11 gene expression is associated with a favorable prognosis in patients with colon adenocarcinoma. This phenomenon may be attributed to a higher proportion of anticancer immune cells in the tumor microenvironment (TME).⁸⁶ Across different datasets, it becomes clear that the levels of CXCL11 expression defy simplistic categorization as merely “good” or “bad”. In summary, the impact of CXCL11 on colorectal cancer is multifaceted, involving diverse pathways and bidirectional effects. The potential avenue for future drug development may be the exploration of CXCL11 as a combinatorial inhibitor with CXCL12.

CXCL11 in Stomach Adenocarcinoma (STAD)

In gastric cancer, adenocarcinoma constitutes 90% of all cases. The most prominent risk factor is Helicobacter pylori infection. This pathogen induces recurrent inflammation of the gastric mucosa, subsequently progressing to atrophic gastritis. The IFN-γ-inducible ELR⁻ CXCR3 ligands are considered to exert an influence on tumor growth by mediating the infiltration of cytotoxic T lymphocytes and suppressing angiogenesis.⁹ In contrast, in vitro experiments have revealed that Helicobacter pylori can suppress the induction of IFN-γ.¹⁰ The CXCL11–CXCR3 axis may upregulate PD-L1 expression in gastric cancer (GC) cells by activating STAT and PI3K– Akt signaling pathways. This could aid the application of checkpoint inhibitors for patients with advanced gastric cancer. Furthermore, a significant positive correlation was observed between PD-L1 and CXCR3 expression levels in gastric cancer tissues.⁸ Moreover, in a study that combined data array analysis and expression detection, CXCL11 was identified as an independent prognostic marker for gastric cancer. Lower expression of CXCL11 was associated with poor prognosis. This could be attributed to a reduction in Th1 activation and alterations in macrophage polarization.¹¹ Hence, CXCL11 appears to play a more proactive role in gastric cancer. Further research into this topic could potentially enhance our understanding of clinical strategies for gastric cancer.

CXCL11 in Liver Cancer (LC)

Similar to gastric cancer, the onset of liver cancer also has distinct risk factors, including alcohol and hepatitis virus infection. Both can cause chronic hepatitis, leading to cirrhosis and ultimately to malignant liver tumors, a progression often referred to as the “trilogy of liver cancer”. In a controlled trial involving patients with chronic hepatitis caused by various etiologies, the serum concentration of CXCL11 was found to be higher than that in the healthy control group and was also found to be significantly elevated in the late stages of cirrhosis.¹⁴ In addition, Chalin, Helbig, and others have found that the expression of CXCL11 is elevated in hepatitis C (CHC).^15,87 Most liver cancers are hepatocellular carcinoma (HCC). Berres et al. further discovered that the level of CXCL11 increases with the severity of liver fibrosis¹⁶ CXCL11 exhibits the capability to engage the CXCR3 receptor located on α2δ1+ Hepatocellular Carcinoma Tumor Initiating Cells (α2δ1+ HCC TICs) through an autocrine secretion mechanism. This instigates the activation of the ERK1/2 signaling pathway, exerting regulatory control over tumor stem cell populations and ultimately sustaining the self-renewal, tumorigenic potential and chemoresistance traits of HCC TICs.¹² In hepatocellular carcinoma cancer-associated fibroblasts (HCC CAFs), CXCL11 secreted by CAFs can promote HCC cell proliferation and migration through the LINC00152-miR-205-5p-CXCL11 axis. In vitro experiments and mouse models showed that LINC00152 knockdown reduced the expression of CXCL11, thereby inhibiting HCC cell vitality, colony formation, and migration ability. In addition, miR-205-5p can bind to the 3′UTR of LINC00152 and CXCL11 RNA, inhibiting the expression of CXCL11. In this context, LINC00152 may act as a ceRNA to counteract the miR-205-5p-mediated inhibition of CXCL11.¹³ Coincidentally, research has found that CXCL11 can also activate the circUBAP2-miR4756-IFIT1/3 axis in tumor cells to promote HCC migration and metastasis.¹³ This suggests that CXCL11 could serve as key mediator integrating CAF cells to influence the invasive ability of HCC. In summary, the role of CXCL11 in the pathogenesis and progression of liver cancer suggests that it could serve as a potential drug target to contribute to patient disease control.

CXCL11 in Bladder Urothelial Carcinoma (BLCA)

Bladder cancer, a high-risk tumor, has an incidence rate in men that is approximately four times that in women. The inner wall of the bladder is mainly composed of epithelial cells, known as urothelial cells. It has been reported that BLCA is one of the most immunogenic tumors. Currently, BCG has become one of the most important biological therapies for treating BLCA. tumor cells may bind and internalize BCG and present BCG and tumor antigens to immune cells through the secretion of chemokines. In this treatment, the CXCL11 gene was significantly upregulated, leading to Th1 chemotaxis. This process ultimately exerts an anti-tumour effect by inducing tumour-suppressive cells (CTLs, NKs, etc.).¹⁸ In muscle invasive bladder cancer (MIBC), high expression of CXCL11-CXCR3alt is associated with high efficacy of neoadjuvant chemotherapy. This may be because highly active CD8⁺ T cells in the tumor microenvironment (especially TSCM) express more CXCR3-alt.¹⁷ The intratumoural CD3 content can predict the abundance of CXCL11, suggesting a potential role of immunogenic cell death (ICD).⁸⁸ Besides, a survival analysis of the GEO and TCGA databases indicated that high levels of CXCL11 mRNA expression are significantly associated with poorer patient overall survival (OS).⁸⁹ These studies could aid in the development of more precise immunotherapeutic strategies for bladder cancer patients in the future, such as T cell adoptive therapy and immune checkpoint inhibitors.

CXCL11 in Renal Carcinoma (RC)

The value of chemokines in targeted therapy for renal cell carcinoma has been confirmed by multiple studies.^90,91 We have also conducted a comprehensive evaluation of the diagnostic, therapeutic, and prognostic capabilities of CXCL11 and its receptors in renal malignancies. Zeng et al. found that EP300/CBP, as a histone acetyltransferase, can modify the promoter of RNA-binding motif protein 15 (RBM15), leading to enhanced expression of RBM15. This process stabilizes the mRNA levels of CXCL11. The secretion of CXCL11 further induces macrophage infiltration and M2 polarization, ultimately promoting the proliferation and migration of clear cell renal cell carcinoma (ccRCC).¹⁹ Research has also found that CXCL11 is highly expressed in the vascular system of human renal cell carcinoma. Given the high affinity of CXCL11 for CXCR3, the CXCL11–CXCR3 axis plays a significant physiological and pathological role in the occurrence and development of renal cell carcinoma. In fact, RT-PCR has also shown significant upregulation of CXC11 and CXCR3 mRNA in RCC samples.²⁰ As another example, a system evaluation model based on ICL scores indicates that overexpression of CXCL11 predicts adverse clinical outcomes in ccRCC patients.⁹² This is consistent with the examples mentioned earlier. A variant splice receptor of CXCL11, CXCR3-B, has been found to have immunovascular inhibitory activity in non-metastatic human renal cell carcinoma.²¹ Therefore, we believe that CXCL11 and its receptors are valuable for the prognostic analysis and targeted therapy of renal cell carcinoma.

CXCL11 in Lung Cancer (LUNG)

Over the past several decades, the concept of early diagnosis and the advent of many novel biopharmaceuticals have greatly improved the survival rate of lung cancer patients. However, lung cancer remains a major health hazard for humans, with an estimated 2 million new cases and 1.76 million deaths annually.⁹³ Immune checkpoint inhibitors (ICIs) play a pivotal role for treating lung cancer. In an animal experiment involving ICI-sensitive cell lines, CXCL11 was upregulated by PD-L1 blockade. Silencing CXCL11 in tumor cells can inhibit the antitumor and vascular inhibitory effects of PD-L1 inhibitors.²² The researchers also used anti-CXCR3 antibodies in conjunction with PD-L1 antibodies and found that blocking CXCR3 can yield similar results. This may be due to the fact that although early treatment with ICIs requires the antitumor ability of CD8⁺ T cell infiltration induced by CXCL11-CXCR3, the antiangiogenic ability of CXCL11 dominates in the late stage. In vitro experiments corroborated this result, with the upregulation of CXCL11 expression stimulated by IFN-γ being associated with sensitivity to PD-L1 receptor blockade. At the same time, serum CXCL11 levels in lung cancer patients may also be a potential biomarker for clinical treatment with ICIs.²² In 2023, through a prospective multicenter study, researchers identified that the early elevation of peripheral blood levels of CXCL11 and IFN-g may serve as indicators for the increased occurrence of immune-related adverse events (irAEs).⁵⁵ This conclusion is primarily drawn from the clinical data of patients with non-small-cell lung cancer (NSCLC) and cutaneous melanoma who underwent ICI treatment. In another comprehensive study on NSCLC, docetaxel increased the release of HMGB1 in a ROS-dependent manner. HMGB1 further stimulated the secretion of CXCL11 by activating NF-κB, ultimately leading to an increase in CD8⁺ T cell infiltration.²³ In a control study that included various types of malignant effusions, CXCL11 was found to be present in higher concentrations in malignant effusions than in non-malignant effusions.⁹⁴ CXCL11 also participates in the malignant biological behavior of lung cancer. The human runt-related transcription factor (RUNX) protein is instrumental in both normal development and tumor progression, among which RUNX3 is a tumor suppressor. The receptor activator of nuclear factor-κB ligand (RANKL) serves as an important pathway to mediate the differentiation of osteoclasts, thereby stimulating bone resorption.⁹⁵ This process requires the binding of RANKL to the receptor activator of nuclear factor-κB (RANK) to initiate, whereas osteoprotegerin (OPG) can prevent this process. Kim et al. found that in non-small-cell lung cancer, knocking out RUNX3 can downregulate CXCL11 mRNA expression. This affects the relative ratio of RANKL/OPG in osteoclasts, increasing the metastasis of tumors to bone tissue.²⁴ This suggests that CXCL11 can also counteract the osteolytic effects of NSCLC. In summary, CXCL11 is closely related to the prognosis of patients with lung cancer, the efficacy of immunotherapy, chemotherapy-induced immune cell infiltration, and anti-malignant biological behavior.

CXCL11 in Head and Neck Squamous Cell Carcinoma (HNSCC) (excluding Oral Carcinoma)

General head and neck tumors encompass three major parts: neck tumors otolaryngological tumours and oral and maxillofacial tumors. Most head and neck tumors are squamous cell carcinomas. Surgery and concurrent chemoradiotherapy are the main treatment methods for HNSCC. However, the era of immuno-oncology also highlights the limitations of traditional preclinical HNSCC models. Lymphatic endothelial cells (LECs) play a crucial role in lymph node metastasis of tumors. Inflammatory LECs in tumors can produce more CXCL11, promoting the expression of various carcinogenic factors such as MMP7. The overexpressed CXCR3 receptor in HNSCC ‘responds’ to these stimuli, activating the JAK-STAT and AKT pathways, further inducing EMT and chemotaxis toward LECs.²⁵ In fact, CXCL11 is widely expressed in head and neck tumor cell lines. Cao et al⁵⁶ found that low expression of an immune-related lncRNA, TRG-AS1, can cause the expression of CXCL11 in the tumor environment, which may be a new marker for predicting the efficacy of PD-1 treatment.In another control experiment on the impact of smoking on HNSCC, tobacco inhibited the expression of CXCR3 ligands in the immune microenvironment. Patients with a history of smoking have a lower number of PD-1+ positive cells, which may be due to the weakened ability of CXCL11 to recruit cytotoxic T cells and NK cells.⁵⁷ In summary, the CXCL11–CXCR3 axis has great potential for treating head and neck squamous cell carcinoma, and the specific inhibition of its expression in tumour cells without affecting the recruitment of immune cells should be a key research objective.

CXCL11 in oral cancer (OC)

Oral squamous cell carcinoma (OSCC) is a common pathological type of oral cancer. In OSCC, the expression of CXCL11 in tumor tissues is increased compared with that in normal tissues, and the content of its receptor subtype CXCR3-A, rather than CXCR3-B or CXCR-alt, is significantly increased. Moreover, the same trend is also observed in important precancerous lesions, oral leukoplakia (OLK). Simultaneously, knocking down CXCL11 inhibits the expression of intracellular immune checkpoints (mainly CD274 and IDO1).²⁶ This could be a potential mechanism causing immune escape in OSCC. Similarly, another receptor of CXCL11, CXCR7, has also been found to have increased expression in OSCC and OLK tissues. The CXCL11–CXCR7 axis is significantly correlated with the developmental stages of oral cancer and may start to play a role from the early stage of malignant transformation in the oral cavity.²⁷ Furthermore, the autoimmune regulator (AIRE) can interact with the oncogene ETS1 to promote the expression of CXCL11 in OSCC, but the mechanism of this mixed transcriptional activation is not yet fully understood.⁹⁶

CXCL11 in Skin Melanoma (SKCM)

Melanoma, the most malignant type of skin cancer, has always been the focus of attention for the development of treatment methods. Melanoma is one of the most sensitive malignant tumors to immune regulation. Although immunotherapy is currently widely used for treating unresectable or metastatic melanoma, its high cost and immune resistance of tumors limit its further clinical promotion. In a comprehensive study combining qRT–PCR and TCGA data analysis, CXCL11 was identified as one of the differentially expressed genes (DEGs) related to immune cell infiltration, and it has a negative correlation with the prognosis of melanoma.²⁸ In a similar fashion, Zhou et al. identified that SKCM patients with a lower transcription level of CXCL11 exhibited a more favorable prognosis in a bioinformatics analysis.²⁹ In an in vitro study using the M24Met melanoma cell line, it was discerned that the receptor CXCR3, a known target of CXCL11, could potentiate the migratory and invasive phenotypes of tumor cells.³⁰ However, researchers have also found that CXCL11 may enhance the immune response to melanoma by recruiting immune cells (CD8⁺ T cells) or serving as a marker for bone marrow activation (MA).^31,97 CD13, a myeloid cell marker and metalloprotease, truncates CXCL11. This truncation not only results in the loss of chemotaxis of lymphocytes such as NK cells but also promotes local angiogenesis in the environment.⁹⁸ Additionally, current research has confirmed that a tumor microenvironment enriched with CD16⁺ macrophages enhances the response to combined PD-1 and CTLA-4 immune therapies. In melanomas with a higher density of CD16⁺ macrophages, an upregulation of CXCL11 gene expression is observed.⁵⁸ This indicates the functional role of CXCL11 in recruiting immune cells. Jacquelot et al. reported that the loss of CXCR3 on circulating T cell subsets was associated with skin or lymph node metastases.⁹⁹ The complexity of CXCL11 function in tumors may be related to the expression location of its receptor CXCR3. The expression of CXCR3 on locally infiltrating immune cells usually inhibits the development of melanoma, but the expression of this receptor on melanoma cells themselves can lead to metastatic invasion. These findings reveal new molecular strategies for the impact of impact on tumors and are expected to further promote the development of immunotherapy in melanoma.

CXCL11 in Other Malignant Tumors

We have also found that I-TAC plays a role in other types of tumors through various pathways. Anti-HER2 monoclonal antibody therapy has an important role in the comprehensive treatment of breast cancer (BC). In HER2 + BC tumourstumors low expression of the IFI16–CXCL11 axis can result in higher drug resistance. Suppression of the STING pathway mediated by Interferon-γ inducible protein 16 (IFI16) can lead to insufficient expression of CXCL11, thereby reducing the infiltration of CD8⁺ T cells and memory T cells.³² If it is possible to ‘reverse’ its abnormal regulation through molecular means, this may be a new direction for future targeted drug research. The serum CXCL11 levels in HR + breast cancer patients are lower than those in HR patients, suggesting that CXCL11 may exhibit HR- dependent regulatory expression in breast cancer.³³ Chu et al. observed in their animal studies that the expression level of I-TAC in breast cancer tissues was downregulated, exhibiting a negative correlation with breast cancer staging. Furthermore, the injection of cells overexpressing I-TAC into juvenile Balb/c mouse tumors ultimately led to tumor regression.³⁴ However, another study found that senescent endothelial cells could enhance the invasiveness of breast cancer cells through the release of the CXCL11–CXCR3 axis. This process is achieved through activation of the ERK pathway.³⁵ Furthermore, intriguing findings suggest that exercise training can enhance the infiltration of CD8⁺ T cells into the tumor microenvironment (TME) through the CXCL11–CXCR3 axis. This augmentation contributes to an increased responsiveness of breast cancer to ICI treatment.⁵⁹ I-TAC can influence the progression of breast cancer through various molecular signaling pathways, and the above evidence provides a new direction for the treatment of breast cancer. In the hematological system, CXCL11 has also been studied in diffuse large B-cell lymphoma (DLBCL), chronic lymphocytic leukemia (CLL), and multiple myeloma (MM). I-TAC can activate tyrosine kinase and induce the secretion of MMP-2 and MMP-9 in MM cells, which contributes to the progression and metastasis of MM. However, if the surrounding immune cells express more CXCR3, then CXCL11 can induce immune-active cells to enter the tumor site and exert anticancer effects.³⁶ The mutation status of the immunoglobulin heavy chain variable region (IGHV-mutated) is a prognostic biomarker related to CLL, and CXCL11 is significantly associated with CLL.³⁷ CXCL11 can also serve as a diagnostic and progression prediction factor for diffuse large B-cell lymphoma. Zhou et al. found that CXCL11 is expressed more in patients with later-stage DLBCL and has a high diagnostic prediction ability (AUC = 1.000).³⁸ Additionally, an animal study demonstrated that CXCL11 can exert an anti-lymphoma effect through the recruitment of CD8⁺ cells.¹⁰⁰ Postmenopausal estrogen replacement therapy is an important risk factor for women to develop ovarian cancer (OV). Estrogen receptor α (ERα) can enhance the expression of the CXCL11–CXCR7 axis and promote EMT and invasion of OV cells in a feed-forward regulatory manner.³⁹ Simultaneously, it has been discovered that CXCL11–CXCR3 is pathologically elevated in OV with pre-lesions of endometriosis. Among them, the CXCR3A subtype is predominantly expressed in cancer cells and infiltrating lymphocytes, which may be related to the suppression of cytotoxic T cells in the local inflammatory environment.^40,41 In pancreatic cancer (PAAD), which can be considered one of the most lethal malignant tumors, serum CXCL11 levels have been found to serve as an effective diagnostic indicator.⁴² Similar findings have been observed in prostate adenocarcinoma (PRAD), where the serum CXCL11 content in patients with advanced prostate cancer is higher than that in healthy controls.⁴³ Basal cell carcinoma is the most common malignant skin tumor. In BCC (Basal Cell Carcinoma) cells, there is a significant upregulation of CXCL11 and all subtypes of its receptor CXCR3. At the same time, CXCL11 has been found in in vitro cell experiments to promote the proliferation of human immortalized keratinocytes. This indicates that the CXCL11–CXCR3 axis is an important signal transduction mechanism in BCC.⁴⁴ The positive feedback loop of CXCL11-EGF-EGFR promotes angiogenesis in anaplastic thyroid carcinoma (THCA), with the receptor CXCR7 involved. This provides a new approach for alotinib-targeted therapy for thyroid cancer.⁴⁵ In papillary thyroid carcinoma (PTC), the release of CXCL11 induced by IFN-γ inhibits tumor proliferation and spread, and PPARγ agonists can also cause similar effects.⁴⁶ However, the role of CXCL11 and its receptors in the aforementioned tumors requires further study.

Discussions

As an important mediator of leukocyte attraction in the body, CXCL11 undoubtedly plays an indispensable role in the tumor microenvironment. In addition to their chemotactic attraction, chemokines can guide the biological functions of immune cells that have receptors. In fact, as an IFN-induced chemokine, it often promotes or inhibits the occurrence and development of tumors by affecting lymphocyte infiltration. Li et al. found that CXCL11 is positively correlated with almost all immune-related genes in almost all cancers.³ The application of immune checkpoint inhibitors such as PD-L1 has been associated with CXCL11 in various tumors. It can be imagined that if a method is found to enhance the release of CXCL11 in the local environment, immune checkpoint inhibitors can play a greater role for treating malignant tumors.

When we are looking for new ‘druggable’ targets in tumor treatment, we are often looking for proteins that can be regulated. Currently, antitumor treatments targeting chemokines and their receptors have been studied in tumors such as breast cancer,¹⁰¹ kidney cancer,⁹⁰ acute lymphoblastic leukemia¹⁰² and ovarian cancer.¹⁰³ At the outset, research on highly targeted therapeutic interventions for CXCL11 did not show significant advancement. However, as investigations progressed, the preclinical challenges associated with CXCL11 and its receptors garnered sustained attention. CXCR3 gained early clinical attention, and in 2009, a randomized double-blind pharmacokinetic study involving 9 volunteers was conducted for the oral administration of AMG 487 (a selective bioavailable CXCR3 antagonist). The study also observed dose- and time-dependent kinetics, particularly at high doses.¹⁰⁴ Melanoma is a highly immunogenic cutaneous malignancy. In addition, melanoma vaccines play a crucial role for treating late-stage patients. A clinical study aimed at evaluating intratumoral injection of IFN-γ during vaccination in patients with metastatic melanoma (Identifier: NCT00977145, https://ClinicalTrials.gov) indicates that IFN-γ can induce the expression on tumor antigen-specific T cells. In subsequent investigations, researchers reiterated that the administration of the peptide vaccine in montanide adjuvant induces peripheral CD8⁺ T cells, with a predominant positive expression of CXCR3.¹⁰⁵ This outcome suggests that enhancing the induction of circulating CXCR3 + immune cells represents a viable avenue for controlling malignant tumors. In studies constructing relevant biological indicators, CXCL11 and its receptors receive comparatively more comprehensive evaluation. A clinical trial measuring the expression levels and prognostic value of CXCR3 in renal cell carcinoma (Identifier: NCT01339975, https://ClinicalTrials.gov) has completed recruitment. They posit that a low CXCR3 tumor expression level is associated with unfavorable prognostic factors in RCC; however, further evidence is required. At present, clinical studies primarily consider CXCL11 as an accompanying indicator for evaluating treatments in metastatic NSCLC, peritoneal surface malignancies, and non-melanoma skin cancer (Identifier: NCT03168464; NCT03458117; NCT02151448, https://ClinicalTrials.gov). Researchers incorporate the levels in peripheral blood or local tissues as crucial indicators for observation. The expression levels of CXCL11 and its receptors may reflect the biological behavior of malignant tumors, providing predictive information on treatment outcomes. In glioblastoma, Wang et al¹⁰⁶ experimentally equipped oncolytic adenoviruses with the chemokine CXCL11 to enhance CAR-T cell infiltration and modify the immunosuppressive TME.These advancements are expected to prompt increased attention from clinical research toward the application of CXCL11 and its receptors in the field of oncology, thereby driving a deeper understanding of chemokine.

The main receptor of CXCL11, CXCR3, has different subtypes. We found that CXCR3-A often promotes the occurrence and migration of tumors through the autocrine axis, whereas CXCR3-B does the opposite. CXCR3 can recruit CTL, NK cells, macrophages and other anti-tumour immune cells to increase the inflammatory response. Simultaneously, CXCR3-B can also inhibit tumor angiogenesis. This process may be mediated by activation of the MAPK pathway.¹⁰⁷ The onset and progression of neoplastic diseases are often associated with dysregulation of the body’s immune functions. In the early tumorigenic microenvironment, the activity of immune cells may be compromised, leading to insufficient immune responses against tumors. In fact, the occurrence of tumors is often accompanied by a change in the ratio of CXCR3-A/CXCR3-B from low to high.⁶² Changes in the tumor microenvironment, such as the degree of inflammation and immune cell infiltration, may influence the expression and activity of CXCR3 subtypes. Dynamically monitoring changes in CXCR3 subtypes can aid in predicting tumor development and behavior, particularly in the significant prediction of tumor migration and metastasis. Furthermore, a comprehensive understanding of CXCR3 subtypes can provide a basis for designing personalized treatment strategies and enhance the predictability of antitumor treatment outcomes. However, as mentioned earlier in this article, the realization of such concepts may pose challenges because of the high structural similarity between CXCR3-A and CXCR3-B. Returning to the discussion, considering the distinct cellular localization of CXCR3 expression, it is hypothesized that the regulation of CXCL11 to selectively bind with a specific receptor holds promising therapeutic potential. We acknowledge that one of the core goals of precision medicine is to avoid unnecessary treatment side effects. By understanding the molecular interaction between CXCL11 and CXCR3 subtypes, it may be possible to circumvent treatment approaches that may not be suitable for certain patients, thus reducing treatment risks. Shifting the topic to CXCR7, as a seven-transmembrane receptor (7TMR), they are the most common targets in medical treatment.¹⁰⁸ Contrary to the long-held belief that CXCR7 could not signal through the traditional heterotrimeric G protein, thereby diminishing its pharmacological significance, this receptor exhibits unique value in malignant tumors such as ovarian cancer or thyroid cancer.^39,45 Initially identified as negative regulators of G protein signaling, β-arrestings were later found to positively regulate cellular signaling. In our evaluation of the medicalization or diaphanization of CXCR7, we may have only focused on the measurement of G protein-mediated effects. In the future, observing the biological characteristics of both G proteins and β-arrestins will help us gain a more comprehensive understanding of CXCR7 pharmacology.

Most of the research on CXCL11 in oncology is based on correlation studies at the molecular expression level, bioinformatics analysis data, and in vitro experiments. There is still a lack of direct evidence to promote its other practical applications. Given the complexity of chemokine regulatory mechanisms, CXCL11 often has a bidirectional effect on tumor development (and often may be the same receptor). Therefore, its clinical application has been in a relatively limited situation for a long time. As mentioned earlier in this article, it is worth exploring agonists or neutralizing antibodies against CXCL11, and even high-targeting antagonists against different receptor subtypes. At the same time, gradually available scientific models are being built. Some clinical studies have used it as an indicator of biological effects. This progress has a positive effect on the ability to establish tumor risk stratification, predict treatment responses and assess patient prognosis. At the same time, the relationship between CXCL11 and chemotherapy resistance sensitivity should not be ignored, and the study of I-TAC’s auxiliary role in existing therapies is also a direction worth exploring. Several prospective studies have clearly indicated that CXCL11 plays an important role in various diseases. However, to deeply understand its specific molecular biological mechanisms and related signaling pathways, further research is required.

Conclusions and Prospects

Tumors are not merely composed of a single type of abnormal cells; rather, they resemble a multidimensional community that brings together members of various cell types. In particular, growing research in recent years has demonstrated that CXCL11 influences tumor cell functions through various downstream signaling pathways. Their aberrant differential expression in malignant tumors results in the recruitment of leukocytes, angiogenesis, epithelial– mesenchymal transition, proliferation, and metastasis of cancer cells, but can also evoke anti-tumor effects. It is worth emphasizing that the role of chemokines is no longer limited to a single molecular regulatory pathway. They can not only serve as independent predictors for diagnosis but also can become new targets for tumor treatment. An in-depth understanding of the molecular mechanisms of CXCL11 in various tumor types will contribute to the design of personalized therapeutic strategies for cancer.

Footnotes

Author Contributions

JW: As the first author, responsible for overall paper writing and organization. XO: Involved in literature review and data collection. Made significant contributions to the content modification and revision of the paper. WZ: Involved in data collection and drew the tables. QY: Designed and drew the figures. Corresponding Author (JZ): Responsible for the research design and supervision, actively participated in paper writing and revision, and took responsibility for the paper’s modifications and submission process and the access to funding. All authors have read and agreed to the published version of the manuscript.

Declaration of conflicting interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This research was funded by the National Natural Science Foundation of China (grant number 82260604) and the Natural Science Foundation of Jiangxi Province (grant number 20192BAB205053).

Ethical Statement

ORCID iD

Jiaqi Wang

Appendix

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The Role of CXCL11 and its Receptors in Cancer: Prospective but Challenging Clinical Targets

Abstract

Plain language summary

Keywords

Introduction

Composition and Role of the Chemokine Family

Structure and Biological Function of CXCL11 and its Receptor

CXCL11

CXCR3

CXCR7

Role of CXCL11 in Human Malignant Tumors

CXCL11 in Colon Adenocarcinoma and Rectal Adenocarcinoma (COADREAD)

CXCL11 in Stomach Adenocarcinoma (STAD)

CXCL11 in Liver Cancer (LC)

CXCL11 in Bladder Urothelial Carcinoma (BLCA)

CXCL11 in Renal Carcinoma (RC)

CXCL11 in Lung Cancer (LUNG)

CXCL11 in Head and Neck Squamous Cell Carcinoma (HNSCC) (excluding Oral Carcinoma)

CXCL11 in oral cancer (OC)

CXCL11 in Skin Melanoma (SKCM)

CXCL11 in Other Malignant Tumors

Discussions

Conclusions and Prospects

Footnotes

Author Contributions

Declaration of conflicting interests

Funding

Ethical Statement

ORCID iD

Appendix

References