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Abstract

NUCKS (nuclear, casein kinase, and cyclin-dependent kinase substrate) is implicated in the tumorigenesis of several human malignancies, but its role in ovarian cancer remains unknown. We aim to investigate NUCKS expression and its clinical significance in ovarian cancer. The messenger RNA expression of NUCKS was determined in normal and malignant ovarian tissues using quantitative polymerase chain reaction assay. Immunohistochemistry was applied to detect the status of NUCKS protein expression in 121 ovarian cancer tissues. NUCKS protein high expression was detected in 52 (43.0%) of 121 patients. NUCKS messenger RNA expression was gradually upregulated in non-metastatic ovarian cancers (n = 20), metastatic ovarian cancers (n = 20), and its matched metastatic lesions (n = 20) in comparison with that in normal ovarian tissues (n = 10; p < 0.05). Elevated expression of NUCKS in ovarian cancer was associated significantly with the Federation of Gynecology and Obstetrics stage (p = 0.037), histological grade (p = 0.003), residual disease (p = 0.013), lymph node metastasis (p = 0.002), response to chemotherapy (p < 0.001), and recurrence (p = 0.013). In the multivariate Cox analysis, NUCKS expression was an independent prognostic marker for overall survival and disease-free survival in ovarian cancer with p values of <0.001 for both. Especially, NUCKS overexpression had prognostic potential for overall survival and disease-free survival (p < 0.001 for both) in advanced ovarian cancers and only for disease-free survival in early ovarian cancers (p = 0.017). Our data suggest that NUCKS overexpression may contribute to progression and poor prognosis in ovarian cancer especially in advanced ovarian cancer.

Keywords

Ovarian cancer NUCKS prognosis lymph node metastasis resistance

Introduction

Ovarian cancer (OC) is the most lethal gynecologic malignancy.¹ Due to a lacking of methods for early detection, nearly 70% of patients present with advanced stage at diagnosis, with a result of poor prognosis. Despite advances in surgery and new chemotherapy regimens during the last few decades, the reported 5-year survival rate for patients with OC was still 25%–30% or even less.^2,3 Identification of new prognostic factors to select patients with good or bad outcome might help improve treatment. However, clinicopathological indicators alone do not enable clinicians to make precise prognoses for individual OC patients. The advent of molecularly targeted therapies, however, could dramatically alter clinical outcome. Thus, novel prognostic and predictive markers are needed to better assess patient outcome and guide individual therapies.

The NUCKS (nuclear, casein kinase, and cyclin-dependent kinase substrate) gene, a vertebrate specific gene, is located on human chromosome 1q32.1 and is a highly phosphorylated protein present in a number of mammalian cell types and tissues.^4–6 NUCKS1 is a chromatin-associated protein with a role in the DNA damage response and in homologous recombination (HR), a DNA repair pathway critical for tumor suppression.⁷ And it was proved to involve in cell-cycle control and DNA repair with regard to the identification of CK2 and PIKK kinases as kinases phosphorylating NUCKS in vivo.⁸ Furthermore, NUCKS is implicated in tumorigenesis, proliferation, invasion, and prognosis of many human malignancies.^9–17 Our previous study had reported that NUCKS overexpressed in endometrial cancer and played a role in predicting prognosis and recurrence.¹⁸ However, up to date, there have been no published reports evaluating its expression in OC tissues and the clinical significance in OC patients.

This study was performed to investigate the expression of NUCKS in OC and to analyze its relationship to various clinicopathological features, including patient outcome.

Materials and methods

Samples and patients

In the current retrospective study, 121 patients with OC who were surgically treated in the Department of Gynecologic Oncology (Harbin Medical University Cancer Hospital, Harbin, China) from January 2008 to December 2009 were enrolled. Fresh tissues from 10 normal ovaries, 20 non-metastatic OCs, 20 metastatic OCs, and their matched metastatic lesions (n = 20) were collected for quantitative polymerase chain reaction (qPCR) analysis. Patients with normal ovaries underwent hysterectomy with oophorectomy for benign uterine disease. All of the patients with OC underwent primary cytoreduction followed by standard platinum-based combination chemotherapy. OC patients without lymph node dissection were excluded in this study. No patients received chemotherapy, radiotherapy, or immunotherapy before the surgery.

All the paraffin-embedded tissues and fresh tissues were taken with the consent from each patient. This study was approved by the Medical Ethics Committee of Harbin Medical University. Clinicopathological features of the OC cohort are outlined in Table 1. Histological typing was carried out according to World Health Organization (WHO) classification standards.¹⁹ The grading and staging of tumors were assigned according to the Federation of Gynecology and Obstetrics (FIGO) rules.²⁰ The status of residual disease was divided into R0 (no residual tumor nodule), R1 (the largest residual tumor nodule measuring 1 cm or less), and R2 (the largest residual tumor nodule measuring more than 1 cm). This definition is the most widely accepted among gynecologic oncologists.

Table 1.

Relationships of NUCKS protein expression status and clinicopathological variables in OC.

Parameters	Patients (n = 121)	NUCKS expression		p value
Parameters	Patients (n = 121)	Low (%; n = 69)	High (%; n = 52)	p value
Age (years)				0.687
≤54	51	28 (54.9)	23 (45.1)
>54	70	41 (58.6)	29 (41.4)
Histological type				0.688
Serous	78	43 (62.8)	35 (37.2)
Mucinous	18	12 (61.1)	6 (38.9)
Endometrioid	16	10 (31.3)	6 (68.7)
Clear cell	9	4 (44.4)	5 (55.6)
FIGO stage				0.037
I	20	13 (85.0)	2 (15.0)
II	26	13 (50.0)	9 (50.0)
III–IV	75	43 (52.0)	41 (48.0)
Histological grade				0.003
G1/G2	44	33 (47.8)	11 (31.8)
G3	77	36 (52.2)	41 (53.2)
Residual disease (RD)				0.013
R0	28	20 (71.4)	8 (28.6)
R1	54	34 (62.9)	20 (37.1)
R2	39	15 (38.5)	24 (61.5)
Ascites				0.379
No	39	20 (51.3)	19 (48.7)
Yes	82	49 (59.8)	33 (40.2)
Serum CA-125 level (U/mL)				0.985
≤35	42	19 (45.2)	23 (57.8)
>35	79	50 (63.3)	29 (36.7)
Lymph node metastasis				0.002
No	54	39 (72.2)	15 (27.3)
Yes	67	30 (44.8)	37 (55.2)
Response to chemotherapy
Platinum sensitive	86	61 (70.9)	25 (29.1)	<0.001
Platinum resistant	35	8 (22.9)	27 (77.1)
Recurrence				0.031
No	76	49 (64.5)	27 (35.5)
Yes	45	20 (44.4)	25 (55.6)

FIGO: the Federation of Gynecology and Obstetrics; G1: well differentiated; G2: moderately differentiated; G3: poorly differentiated; OC: ovarian cancer.

All the patients were followed up on regular basis and the last follow-up was carried out in December 2015, with the median observation period of 44 months (2–92 months) and 79 cancer-related deaths.

Immunohistochemical staining and evaluation

Immunohistochemistry staining was carried out using the Two-Step IHC Detection Reagent Kit (Zhong Shan Golden Bridge Biological Technology Inc., Beijing, China) following the manufacturer’s protocols. Experimental steps had been described in our previous study¹⁸ with a primary antibody specific for NUCKS (dilution 1:700; Abcam, Cambridge, MA, USA). Two independent pathologists blinded to the clinical variables conducted the immunoreactivity score for NUCKS expression. When there was disagreement, a senior pathologist was reached until a consensus. Immunoreactivity was scored by counting the percentage of positive cells as follows:¹⁸ 0, fewer than 10% of positive nuclei of epithelial cells were detected; 1, 11%–30% were detected at low staining intensity; 2, more than 30% but less than 60% were detected with moderate staining intensity; and 3, more than 60% of positive nuclei were detected with high staining intensity. For statistical analysis, the score of NUCKS expression was defined as low expression if the overall score was 0–1 and high expression if the sum was 2–3.

RNA extraction, reverse transcription, and qPCR

Total RNA from fresh tissues was extracted using the TRIzol reagent (Invitrogen, Carlsbad, CA) according to the manufacturer’s instruction. About 2 µg RNA from each sample was used for complementary DNA (cDNA) synthesis with 2× Power Taq PCR MasterMix kit (PR1702; BioTeke, Beijing, China). qPCR was employed to quantify the fold change of NUCKS messenger RNA (mRNA) level by Exicycler 96 real-time reverse transcription polymerase chain reaction (RT-PCR) system (Bioneer, Daejeon, Korea) with SYBR Green Mastermix (SY1020; Solarbio, Beijing, China). Expression data were normalized to the geometric mean by β-actin. The qPCR primers for NUCKS were listed as follows: forward, 5′-TCTGATGATGCAGATGAAGATTA-3′; reverse, 5′-CTGCTGAGTGAGAATCATCC-3′. The primers for β-actin were also listed as follows: forward, 5′-CTTAGTTGCGTTACACCCTTTCTTG-3′; reverse, 5′-CTGTCACCTTCACCGTTCCAGTTT-3′. All genes were tested in triplicate.

Statistical analyses

All statistical analyses were carried out with SPSS software package (Chicago, IL, USA, 17.0). For continuous variables, student’s t-test was performed. The chi-square test and Fisher’s test were used to analyze the differences in categorical variables. Survival curves were plotted by the Kaplan–Meier method and compared by the log-rank test. Multivariate survival analysis was carried out for all the variables that were significant in the univariate analysis using the Cox regression model. A two-sided probability value of p < 0.05 was considered statistically significant.

Results

Elevated expression of NUCKS mRNA in OC tissues

To investigate the potential role of NUCKS in the tumorigenesis, qPCR was carried out in normal ovarian tissues (n = 10), non-metastatic OCs (n = 20), metastatic OCs (n = 20), and its matched metastatic lesions (n = 20). As shown in Figure 1(a), NUCKS mRNA level was gradually increased from normal ovarian tissues to primary carcinomas and from non-metastatic OCs to metastatic OCs (p < 0.001 for all). Furthermore, NUCKS mRNA expression was concomitantly upregulated from metastatic OCs to its matched metastatic lesions (p = 0.001, Figure 1(b)).

Figure 1.

(a) Comparison of NUCKS mRNA relative expression levels in normal ovary (N = 10), non-metastatic ovarian cancer (OC; nT = 20), metastatic OC (mT = 20), and its matched metastatic lesion (M = 20). (b) Increased trend of NUCKS mRNA expression in metastatic OC and its matched metastatic lesion.

NUCKS expression and its association with the clinicopathological features of OC

NUCKS was localized in the nuclei of tumor cells (Figure 2). In a few slides, weak or moderate NUCKS expression was observed in cytoplasm of tumor cells accompanied by nuclear staining of tumor cells. In the same specimen, nuclear staining intensity in tumor cells is higher than cytoplasm. Of the OC specimens examined, low nuclear NUCKS expression was detected in 69 (57.0%) of 121 patients, whereas high nuclear NUCKS expression was detected in 73 (43.0%) of 121 patients.

Figure 2.

The representative images for NUCKS protein expression. (a) Low expression in ovarian cancer (OC). (b) High expression in OC. (c) Low expression in non-metastatic OC. (d) High expression in metastatic OC.

Significant correlation was observed between NUCKS expression level and several prognostic risk factors such as FIGO stage (p = 0.037), histological grade (p = 0.003), residual disease (p = 0.013), and lymph node metastasis (p = 0.002). Furthermore, response to chemotherapy (p < 0.001) and recurrence (p = 0.013) was correlated with NUCKS expression level (Table 1).

Survival analysis for the prognosis of patients with OC

To assess NUCKS as a predictor of survival, the Kaplan–Meier analysis method was used to investigate the correlation between NUCKS expression and overall survival (OS)/disease-free survival (DFS). The log-rank test showed that the 5-year OS and DFS rates were 18.8% and 15.2%, respectively, in patients with a high level of NUCKS expression, compared with the 53.4% and 49.4% in their counterparts (p < 0.001 for both). In addition to NUCKS, FIGO stage (p < 0.001), histological grade (p = 0.001), residual disease (p < 0.001), and lymph node metastasis (p < 0.001) are correlated with prognosis of OC (Table 2). We also performed a stage-stratified analysis and revealed that NUCKS overexpression was significantly associated with both OS and DFS (p < 0.001 for both) in advanced OC (FIGO stages III–IV). In early-stage OC (FIGO stages I–II), it only had prognostic value of DFS (p = 0.017) instead of OS (p = 0.079; Figure 3).

Table 2.

Univariate survival analysis of OS and DFS in 121 patients with OC.

Parameters	OS		p value	DFS		p value
Parameters	Mean ± SE	5 years (%)	p value	Mean ± SE	5 years (%)	p value
Age (years)			0.806			0.639
≤54	49.360 ± 4.485	29.4		40.597 ± 4.863	29.2
>54	50.263 ± 4.235	42.9		43.534 ± 4.326	37.9
Histological type			0.253			0.182
Serous	49.999 ± 4.076	40.9		44.761 ± 4.323	38.9
Mucinous	55.389 ± 8.350	50.0		48.872 ± 8.384	46.2
Endometrioid	53.312 ± 5.670	43.8		37.281 ± 6.056	21.9
Clear cell	30.889 ± 6.247	11.1		20.778 ± 6.228	11.1
FIGO stage			<0.001			<0.001
I	88.800 ± 3.091	93.3		88.571 ± 3.304	92.9
II	70.091 ± 5.969	59.1		69.721 ± 7.483	56.7
III–IV	36.183 ± 3.013	23.3		28.299 ± 2.901	17.6
Histological grade			0.002			0.001
G1/G2	64.826 ± 4.302	56.4		57.645 ± 5.117	50.0
G3	41.417 ± 3.880	28.4		33.733 ± 3.840	25.5
Residual disease (RD)			<0.001			<0.001
R0	68.123 ± 4.745	60.7		62.165 ± 5.976	58.9
R1	59.794 ± 4.398	51.4		51.164 ± 4.787	44.1
R2	22.385 ± 3.599	5.10		16.064 ± 3.144	3.80
Ascites			0.386			0.344
No	43.974 ± 5.875	33.3		36.850 ± 5.654	32.8
Yes	52.639 ± 3.553	41.2		44.824 ± 3.908	35.1
Serum CA-125 level (U/mL)			0.233			0.206
≤35	43.857 ± 5.398	31.0		37.364 ± 5.696	29.0
>35	51.576 ± 3.528	42.6		44.753 ± 3.839	37.4
Lymph node metastasis			<0.001			<0.001
No	70.977 ± 3.972	66.7		67.312 ± 4.443	62.6
Yes	32.430 ± 3.270	15.4		23.202 ± 3.124	11.5
NUCKS expression			<0.001			<0.001
Low	62.907 ± 3.646	53.4		57.120 ± 4.190	49.4
High	32.607 ± 4.290	18.8		20.980 ± 2.967	15.2

FIGO: the Federation of Gynecology and Obstetrics; G1: well differentiated; G2: moderately differentiated; G3: poorly differentiated; OS: overall survival; DFS: disease-free survival; OC: ovarian cancer; SE: standard error.

Figure 3.

Subgroup analyses for the overall survival (OS) and disease-free survival (DFS) of ovarian cancer (OC) patients with high and low NUCKS expression: (a) OS in all OCs, (b) DFS in all OCs, (c) OS in early-stage OCs, (d) DFS in early-stage OCs, (e) OS in advanced-stage OCs, and (f) DFS in advanced-stage OCs.

Multivariate Cox regression analysis showed that the high NUCKS expression was considered as an independent prognostic marker for both OS and DFS of patients with OC (p = 0.003 and p < 0.001, respectively; Table 3). Other variables such as FIGO stage (p = 0.001 and p = 0.002, respectively), residual disease (p = 0.002 for both), and lymph node metastasis (p = 0.003 and p < 0.001, respectively) were also identified as independent prognostic factors for OS and DFS.

Table 3.

Multivariate survival analysis of OS and DFS in 121 patients with OC.

Parameters	OS			DFS
Parameters	HR	95% CI	p value	HR	95% CI	p value
FIGO stage			0.001			0.002
I	1.000			1.000
II	6.360	0.799–50.608	0.080	8.676	1.088–69.189	0.041
III–IV	17.169	2.337–126.131	0.005	20.183	2.725–149.491	0.003
Residual disease (RD)			0.002			0.002
R0	1.000			1.000
R1	1.317	0.674–2.573	0.421	1.455	0.740–2.860	0.277
R2	2.962	1.470–5.968	0.002	3.096	1.525–6.285	0.002
Lymph node metastasis
No	1.000			1.000
Yes	2.442	1.364–4.372	0.003	3.043	1.700–5.447	<0.001
NUCKS expression
Low	1.000			1.000
High	2.028	1.270–3.238	0.003	2.891	1.765–4.733	<0.001

FIGO: the Federation of Gynecology and Obstetrics; OS: overall survival; DFS: disease-free survival; OC: ovarian cancer; HR: hazard ratio; CI: confidence interval.

Discussion

In this study, we showed, for the first time, that the expression of NUCKS was gradually upregulated in non-metastatic OCs, metastatic OCs, and its matched metastatic lesions at mRNA level in comparison with that in normal ovarian tissues. High expression level of NUCKS was significantly associated with FIGO stage, histological grade, residual disease, lymph node metastasis, response to chemotherapy, and recurrence. High expression level of NUCKS served as independent prognostic factors for short OS and DFS rates in patients with OC. Moreover, a stage-stratified analysis showed that NUCKS overexpression correlated with DFS in early-stage OC, OS and DFS in advanced-stage OC. In the light of these findings, we demonstrated that NUCKS has the potential to be a novel predictor of progression as well as survival in OC patients.

Increased NUCKS expression has been reported in several cancers,^11–18,21 including OC.⁹ However, the dynamic and complex phosphorylation of NUCKS implies that NUCKS has the possibility to interact with several binding partners and hence being involved in multiple biological functions. NUCKS overexpression was observed in the majority of invasive carcinomas, including atypical ductal hyperplasia, ductal carcinoma in situ, and invasive ductal cancer.^11,22 Also, it was associated with high-invasive phenotype in mouse lung adenocarcinoma cell strains.¹⁰ Furthermore, increased NUCKS expression was associated with high-invasive factors in cervical cancer¹³ and was highly upregulated in colon cancer patients with distant metastasis.¹² A similar observation was also made in gastric cancer tissue. In addition to that NUCKS correlated with high-invasive factors such as FIGO stage, histological grade, residual disease, and lymph node metastasis in OC, we interestingly found that NUCKS mRNA expression gradually increased in tissues as follows: normal ovary, non-metastatic OC, metastatic OC, and its matched metastatic lesion. Furthermore, elevated NUCKS protein expression indicated a suboptimal cytoreduction in OCs with larger residual disease. All these may indicated a significant role of this gene in the neoplastic progression.

NUCKS appears to be important for cell-cycle progression²³ and is involved in facilitating and maintaining the transcription activity of some genes during rapid proliferation.⁹ NUCKS as well as p53 is phosphorylated on multiple sites in proliferating cells in vivo.^4,24,25 Zduniak et al.¹⁵ emphasized that NUCKS abundance in malignant skin tumors is higher than that of the well-known proliferation marker Ki67, thus suggesting that NUCKS protein as a novel proliferation marker for skin tumor specimens. In gastric cancers, NUCKS expression was associated with Ki67 and the combination of these two makers might further distinguish a subgroup of patients with poor prognosis.¹⁴ Additionally, there is evidence that the NUCKS might be involved in facilitating and maintaining the activity of transcription of some genes.^9,21 However, what is the exact underlying mechanism of the interaction of NUCKS with Ki67 remains to be clarified.

To further characterize the clinically prognostic implication of NUCKS in OC, we used stage-stratified analysis to evaluate the prognostic value of NUCKS protein expression. The data suggest that NUCKS provide a prognostic potential in OC especially in advanced OC. NUCKS overexpression was associated with recurrence-related survival in cervical cancer, endometrial cancer, colon cancer, and gastric cancer. Yet, its overexpression served as a predictor of overall survival only in endometrial cancer and gastric cancer in addition to advanced OC.

In our study, we also reported that NUCKS overexpression was associated with response to platinum-based chemotherapy. In accordance with this finding, Shen et al.¹⁷ showed that miR-137 sensitizes chemosensitivity to paclitaxel and cisplatin in lung cancer through inhibiting PI3K/AKT pathways via targeting NUCKS1. The levels of NUCKS correlated with the levels of Bax and activated caspase-3, which are indicative of apoptosis. Moreover, NUCKS was upregulated very early during neuronal apoptosis in vitro.²⁶ These suggest that NUCKS plays complex roles in cell homeostasis.

Taken together, we believe that this study provides the first clinical evidence that NUCKS is an independent prognostic marker for OS and DFS in OC patients. Our findings suggest that NUCKS is highly associated with progression, response to chemotherapy, and prognosis; is a new biomarker for this disease; and is a potential therapeutic target.

Footnotes

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 study was supported by the grants of National Natural Science Foundation of China (81502225), the Postdoctoral Foundation of China (2015M581480), the Postdoctoral Foundation of Heilongjiang Province of China (LBH-Z15123), the Haiyan Foundation of Harbin Medical University Cancer Hospital (JJMS2016-01), the Innovation Foundation for Talents of Harbin Medical University (2016lczx77), and the Youth Elite Training Foundation of Harbin Medical University Cancer Hospital (JY2016-03).

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NUCKS nuclear elevated expression indicates progression and prognosis of ovarian cancer

Abstract

Keywords

Introduction

Materials and methods

Samples and patients

Immunohistochemical staining and evaluation

RNA extraction, reverse transcription, and qPCR

Statistical analyses

Results

Elevated expression of NUCKS mRNA in OC tissues

NUCKS expression and its association with the clinicopathological features of OC

Survival analysis for the prognosis of patients with OC

Discussion

Footnotes

Declaration of conflicting interests

Funding

References