J Cancer 2019; 10(1):131-137. doi:10.7150/jca.28216

Research Paper

Prognostic Value of PDZ-Binding Kinase/T-LAK Cell-Originated Protein Kinase (PBK/TOPK) in Patients with Cancer

Yi Zhang, Xianjin Yang, Rong Wang Corresponding address, Xu Zhang Corresponding address

Department of General Surgery, the First People's Hospital of Neijiang, Neijiang 641000, Sichuan Province, P. R. China.

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How to cite this article:
Zhang Y, Yang X, Wang R, Zhang X. Prognostic Value of PDZ-Binding Kinase/T-LAK Cell-Originated Protein Kinase (PBK/TOPK) in Patients with Cancer. J Cancer 2019; 10(1):131-137. doi:10.7150/jca.28216. Available from http://www.jcancer.org/v10p0131.htm

Abstract

Background: PDZ-binding kinase/T-LAK cell-originated protein kinase (PBK/TOPK) plays a critical role in tumorigenesis and cancer progression. However, the prognostic roles in cancer patients are inconsistent or even controversial. Therefore, we performed a meta-analysis to investigate the prognostic value of PBK/TOPK in cancers.

Methods: Literature search was performed using several online databases (PubMed, Web of Science, Embase, Cochrane Library, and Google Scholar, National Knowledge Infrastructure and Wanfang) for eligible articles published up to May 1, 2018. The relationship between PBK/TOPK expression and prognosis in cancers was investigated by using pooled hazard ratios (HRs) with 95% confidence intervals (CIs) through STATA 12.0 software.

Results: Totally 20 eligible studies were included in this meta-analysis. The pooled results showed that carriers with high protein expression of PBK/TOPK were significantly associated with poor OS (HR: 1.69, 95% CI: 1.33-2.04) in various cancers, and patients with increased PBK/TOPK protein expression were significantly correlated with inferior RFS (HR: 1.63, 95% CI: 1.02-2.24) and short DFS (HR: 1.69, 95% CI: 1.16-2.23).

Conclusions: The findings suggest that PBK/TOPK protein expression might serve as a prognostic tumor marker in cancers.

Keywords: PBK/TOPK, solid tumor, prognosis, meta-analysis

Introduction

PBK (PDZ-binding kinase), also known as T-lymphokine-activated killer cell-originated protein kinase (TOPK), is a 322 amino-acid and mitogen- activated serine/threonine protein kinase [1-2]. PBK/TOPK protein is generally difficult to detect in normal tissues but frequently elevated in cancer tissues, such as breast cancer, lymphoma and bladder cancer [3-5]. Furthermore, PBK/TOPK has been reported to play vital roles in inflammation, cell apoptosis, and cell-cycle regulation and high expression of PBK/TOPK contributes to tumor growth, proliferation, and metastasis [6-9]. Accumulating evidence has reported that PBK/TOPK protein expression was correlated with clinical outcomes in various solid cancers, such as colorectal cancer, cholangiocarcinoma and lung cancer [10-12]. However, the potential prognostic value of PBK/TOPK in human solid tumors is inconsistent and even contradictory. For example, Hayashi et al [13] reported that over-expression of TOPK protein was significantly related with poor prognosis in glioma, which was consistent with the results conducted in lung adenocarcinoma by Wei et al [12], but there was no significant association between PBK/TOPK protein expression and OS in prostate, gastric and epithelial ovarian cancer [14-16]. Conversely, PBK/ TOPK up-regulation was reported to be correlated with longer overall survival in cholangiocarcinoma and oral squamous cell carcinoma [10,17].

To date, there is no study to comprehensively assess the correlation between PBK/TOPK protein expression and prognosis in cancer patients. And considering the limited number of individual study and varied results. Herein, we conducted the meta-analysis with published data to clarify the influence of high PBK/TOPK expression and its impact on the outcomes of different cancers as well as provide an overview of the current roles of PBK/TOPK in tumor prognosis and as a promising therapeutic target.

Materials and Methods

Search strategy and study selection

The literature search was performed by two authors (Zhang Y and Wang R) in the electronic platforms of PubMed, Web of Science, Embase, Cochrane Library, Google scholar, Wanfang and National Knowledge Infrastructure (CNKI). The last search date was May 1, 2018. The search strategy was used as: 'PDZ binding kinase', 'PBK', 'TOPK', 'T-LAK cell-originated protein kinase', 'lymphokine-activated killer T-cell-originated protein kinase', 'Nori-3 protein', 'TOPK' and 'cancer', 'tumour', 'carcinoma', 'neoplasm', 'tumor', 'neoplasia'. Article language was limited to English and Chinese. The references of all relevant articles were manually reviewed to find potentially relevant studies.

Inclusion criteria

(1) studies concerning the prognostic values of PBK/TOPK protein expression in tissues from primary solid cancer; (2) studies with complete information for assessment of hazard ratios (HRs) and their 95% confidence intervals (CIs) for overall survival (OS), progression-free survival (PFS), disease-free survival (DFS) or recurrence-free survival (RFS); (3) original articles in English or Chinese.

Exclusion criteria

(1) articles focused on hematologic neoplasms; (2) study only detected the mRNA expression of PBK/TOPK; (3) letters, editorials, case reports, reviews, comments or abstracts.

Data extraction and quality assessment

The following extracted information was recorded by two independent authors (Zhang Y and Wang R): first author's surname, publication year, number of sample size, number of patients with overexpression of PBK/TOPK protein, country or region, clinical stage or tumor grade, detection method, cut-off value, analytical method, HRs with their 95 % CIs for OS/RFS/DFS/PFS.

To evaluate the quality of studies, the Newcastle- Ottawa Scale (NOS) was applied. We assigned the studies of high quality a scored ≥6.

Statistical analysis

In the meta-analysis, the pooled HRs and their 95% CIs were calculated to investigate the impact of PBK/TOPK expression on the survival of patients using STATA (Version 11.0; StataCorp, College Station, TX). I2 test and Q test were used to assess heterogeneity among the studies, Phet<0.10 and/or I2 > 50% indicates obvious heterogeneity among studies, and then the random effect model was used for significant heterogeneity. Otherwise, a fixed-effect model was applied. Egger's test and Begg's test were conducted to assess potential publication bias. Sensitivity analysis was carried out to explore the stability of the combined results. A p-value < 0.05 was considered as statistically significant.

Results

The study selection procedure is outlined in Figure 1. According to the selection criteria, the potential relevant full-texts were reviewed and further examined. Finally, 20 [10-29] eligible studies which fulfilled all inclusion criteria were selected into this systematic review and meta-analysis.

Up to 3470 participants from 20 studies were enrolled in this meta-analysis. The included articles were published from 2010 to 2018. The sample size varied from 24 to 520. A total of 20 studies investigated the association of PBK/TOPK expression with overall survival (OS) [10-29], and for the correlations between PBK/TOPK expression and secondary outcomes, 2 studies reported progression-free survival (PFS) [13, 16], 3 studies focused on recurrence-free survival (RFS) [12, 20, 28] and 4 studies covered disease-free survival (DFS) [18, 22, 24, 29]. As for cancer type, 12 different kinds of human solid cancers were investigated, including colorectal cancer (CRC) [10, 22, 25], cholangiocarcinoma (CCA) [11], lung cancer (LC) [12, 18, 19, 21], breast cancer (BC) [20], prostate cancer (PCa) [14, 28], oral squamous cell carcinoma (OSCC) [17], epithelial ovarian cancer (EOC) [16], esophageal squamous cell carcinoma (ESCC) [23], nasopharyngeal carcinoma (NPC) [24], gastric cancer (GC) [15, 26, 27], hepatocellular carcinoma (HCC) [29] and glioma [13]. The principal characteristics of all included studies are summarized in Table 1.

PBK/TOPK protein and OS

A total of 20 studies with 3470 patients reported the relationship between PBK/TOPK protein and OS in various cancers. The random-effects model was applied for large heterogeneity existed (I2 = 71.7%; Phet =0.000). As shown in Figure 2, the overall results showed that high PBK/TOPK expression was significantly correlated with poorer OS in various cancers (HR: 1.69, 95% CI: 1.33-2.04).

 Figure 1 

Flow diagram of studies selection procedure.

J Cancer Image (Click on the image to enlarge.)
 Figure 2 

Forest plots of PBK/TOPK protein and OS in various cancers.

J Cancer Image (Click on the image to enlarge.)
 Table 1 

Characteristics of eligible studies in this meta-analysis.

First authorYearCancer typeCountrySample sizeNumber of OEClinical stage/ tumor gradeCriterion of OETest methodsOutcome measuresMVANOS score
Zlobec et al [10]2010CRCSwitzerland8736NAdiffuse cytoplasmic TOPK staining in >90% of colorectal tumor cellsIHCOSYes6
He et al [11]2010CCAChina2411tumor grade 1-2-3> the percentages of TOPK-positive cells (10 %)IHCOSYes6
Wei et al [12]2012LACChina203136IIHC score >3IHCOS, RFSYes7
Shih et al [18]2012LCChina11972I-II-III-IVIHC score (2, 3)IHCOS, DFSYes6
Lei et al [19]2013NSCLCChina279125I-II-III-IV> the median percentage of positively stained cells ( 11.5%)IHCOSYes8
O Leary et al [20]2013BCIreland290104tumor grade 1-2-3percentage of cells stained multiplied by intensity score >48IHCOS, RFSYes8
Lei et al [21]2015LACChina12767I-II-III-IV> the average percentages of TOPK-positive cells (13.3%)IHCOSYes7
Chen et al [14]2015PCaChina98NANAimmunoreactivity scores (IRS)IHCOSNo6
Xiao et al [22]2015CRCChina186135tumor grade 1-2-3IHC score >3IHCOS, DFSYes7
Chang et al [17]2016OSCCChina28775I-II-III-IVmean PBK/TOPK expression scoreIHCOSYes7
Ikeda et al [16]2016EOCJapan16384I-II-III-IV2+, 3++IHCOS, PFSNo7
Ohashi et al [23]2016ESCCJapan54100-I-II-III-IVintensity plus proportion scores ≥5IHCOSYes6
Wang et al [24]2016NPCChina18592NANAIHCOS, DFSYes7
Zou et al [25]2017CRCChina8043NANAIHCOSNo6
Kwon et al [15]2017GCKorea38579I-II-III+,++IHCOSYes8
Su et al [26]2017GCChina7973I-II-III-IV+,++,+++,++++IHCOSNo6
Ohashi et al [27]2017GCJapan14424I-II-IIIPBK/TOPK presenting scores ⩾5 tumor cellsIHCOSYes7
Pirovano et al [28]2017PCaUK128NANA> the median score of PBK IHC scoreIHCOS, RFSYes7
Yang et al [29]2017HCCChina520292I-II-III-IV> the median score of PBK IHCIHCOS, DFSYes8
Hayashi et al [13]2018GliomaJapan3223II--III-IV> median percentage of TOPK-positive cells (12.7%)IHCOS, PFSYes6

CRC: colorectal cancer; CCA: cholangiocarcinoma; LAC: lung adenocarcinoma; LC: lung cancer; NSCLC: non-small-cell lung cancer; BC: breast cancer; PCa: prostate cancer; OSCC: oral squamous cell carcinoma; EOC: epithelial ovarian cancer; ESCC: esophageal squamous cell carcinoma; NPC: nasopharyngeal carcinoma; GC: gastric cancer; HCC: hepatocellular carcinoma; IHC: immunohistochemistry; OS: overall survival; RFS: recurrence-free survival; PFS: progression-free survival; DFS: disease-free survival; OE: over-expression; MVA: multivariate analysis NA: not available.

We also investigated the prognostic values of PBK/TOPK in several subgroups (Table 2). We found that PBK/TOPK expression level could serve as a prognostic biomarker in lung cancer (HR=2.30, 95% CI: 1.79-2.81) and CRC (HR=2.39, 95% CI: 1.81-2.97). However, there was no significant difference but a strong trend between PBK/TOPK expression level and OS in prostate cancer (HR=1.61, 95% CI: 0.12-3.10) and gastric carcinoma (HR=1.13, 95% CI: 0.86-1.41). Furthermore, increased expression of PBK/TOPK was related to poor OS in Asia cohorts (HR=1.65, 95% CI: 1.28-2.03) but no significant association was found for European cohorts (HR=2.08, 95% CI: 0.94-3.23). Interestingly, PBK/TOPK expression could be an independent predictor for OS in multiple cancers (HR=1.88, 95% CI:1.42-2.34).

PBK/TOPK protein and DFS/PFS/RFS

The pooled HR for secondary outcomes in cancer patients are presented in Table 3.

Patients with elevated expression of PBK/TOPK protein were significantly associated with inferior RFS (HR: 1.63, 95% CI: 1.02-2.24) and shorter DFS (HR: 1.69, 95% CI: 1.16-2.23), and there was a strong trend but not statistical difference between PBK/TOPK expression and PFS (HR: 2.56, 95% CI: 0.80-4.32).

Publication bias

We performed the Begg's and Egger's test to identify potential publication bias. The visible plots were shown in Figure 3 and Figure 4, the test results all indicated that there was no significant publication bias in this meta-analysis (Pr Begg's test > |z| = 0.538 (continuity corrected); Pr Egger's test > |z|=0.111).

Sensitivity analysis

The results (Figure 5) showed that the exclusion of any individual study did not change the statistical significance, suggesting the robustness of our results.

 Figure 3 

Begg's funnel plot for OS.

J Cancer Image (Click on the image to enlarge.)
 Figure 4 

Egger's publication bias plot for OS.

J Cancer Image (Click on the image to enlarge.)
 Figure 5 

Sensitivity analysis for OS.

J Cancer Image (Click on the image to enlarge.)
 Table 2 

Meta-analysis results of the relationship between PBK/TOPK protein and OS.

Group/ subgroupNo. of data setNo. of casesPooled HR (95%CI)p-valueModelPhetI² (%)
Overall [10-29]2034701.69 (1.33-2.04)<0.001Random71.70.0
Lung cancer [12, 18, 19, 21]47282.30 (1.79-2.81)<0.001Fixed0.5240.0
Prostate cancer [14, 28]22261.61 (0.12-3.10)NSFixed0.8530.0
Gastric carcinoma [15, 26, 27]36081.13 (0.86-1.41)NSFixed0.14149
Colorectal cancer [10, 22, 25]33532.39 (1.81-2.97)<0.001Fixed0.6430.0
European cohorts [10, 20, 28]35052.08 (0.94-3.23)NSFixed0.5930.0
Asia cohorts [11-19, 21-27, 29]1729651.65 (1.28-2.03)<0.001Random0.00074.9
Multivariate analysis [10-13, 15, 17-24, 27-29]1630501.88 (1.42-2.34)<0.001Random0.00077.0
 Table 3 

Analyses of secondary outcomes for PBK/TOPK protein in tumors.

Secondary outcomesNo. of data setNo. of casesPooled HR (95% CI)p-valueModelPhetI2 (%)
RFS [12, 20 ,28]36211.63 (1.02-2.24)<0.001Fixed0.4900.0
DFS [18, 22, 24, 29]410101.69 (1.16-2.23)<0.001Fixed0.6770.0
PFS [13, 16]21952.56 (0.80-4.32)NSFixed0.5940.0

Discussion

Since the prognosis potential of PBK/TOPK protein in human solid cancers is inconsistent and debatable, a quantitative meta-analysis is employed in our study. To our knowledge, this is the first meta-analysis to comprehensively evaluate the effect of PBK/TOPK protein level on prognosis in various tumors. By searching against several online databases, a total of 20 observational studies were ultimately included in our work altogether 3470 subjects, containing 12 different cancer types. After analyzing the data extracted from those eligible articles, we revealed that PBK/TOPK protein expression level was associated with clinical outcomes in solid tumors.

The pooled HR results suggested that a high expression level of PBK/TOPK protein was significantly associated with poor OS (HR: 1.69, 95% CI: 1.33-2.04) in human cancers. According to different cancer types, we found the prognostic value of PBK/TOPK in LC (HR=2.30, 95% CI: 1.79-2.81) and CRC (HR=2.39, 95% CI: 1.81-2.97). But no significant differences were found between PBK/TOPK expression and OS in prostate and gastric cancer, this might be for the relatively small number of studies and needed to be explored by future larger studies. As for different ethnicities, the current findings showed that PBK/TOPK expression might be a significant prognostic predictor in Asian patients but not in Caucasian populations, the findings of different ethnic background should be confirmed by future multi-center researches. In addition, we also found that PBK/TOPK protein might be an independent predictor for OS in human cancers (HR=1.88, 95% CI:1.42-2.34). Meanwhile, the relationships between PBK/TOPK protein level and secondary outcomes were also investigated, and PBK/TOPK was found to be a useful prognostic factor for RFS (HR: 1.63, 95% CI: 1.02-2.24) and DFS (HR: 1.69, 95% CI: 1.16-2.23), but not significant for PFS (HR: 2.56, 95% CI: 0.80-4.32). Generally, PBK/TOPK exhibited the potential clinical utility as a candidate molecular marker in human malignancies.

This present study showed that PBK/TOPK expression was associated with patients' clinical outcomes. A number of researches have studied the roles of PBK/TOPK in cancer development, PBK/TOPK acts as an oncogene in multiple cancers and contributes to tumor progression [8, 21, 23, 30-31]. PBK/TOPK is reported to be highly expressed in cancer tissues and cell lines, and high PBK/TOPK expression tends to indicate higher biological malignant aggressiveness [19, 32]. TOPK knockdown could significantly inhibit tumor growth, invasion and metastasis in vitro and in vivo, conversely, PBK up-regulation displays multiple tumorigenic properties, it could promote cell growth, metastasis and enhance tumor transformation [23-26, 30-31]. PBK/TOPK also correlates with drug response and tumor resistance and showed to be the valid target for antineoplastic kinase inhibitors and serves as a potential therapeutic target for various cancers, such as CRC [33-36], lung cancer [37-38], breast cancer [39] and prostate cancer [40-41].

Nevertheless, there are several limitations in our study. First, we only included the studies published in English or Chinese, and most of the studies included came from the Asian countries. Second, the total sample size was not sufficient enough and all enrolled were retrospective studies. Third, the prognostic potentials of PBK/TOPK protein in other special types of cancers were needed for further investingation. Fourth, there was obvious heterogeneity for OS. Finally, the definition of PBK/TOPK protein overexpression varied in different studies.

In summary, the current meta-analysis indicates that elevated PBK/TOPK protein expression is correlated with poor cancer prognosis, and PBK/TOPK protein might be a promising candidate to predicate the cancer survival. If replicated in future larger-scale, multicenter prospective studies, this finding may support the clinical value of PBK/TOPK as a biomarker in tumors.

Competing Interests

The authors have declared that no competing interest exists.

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Author contact

Corresponding address Corresponding authors: Rong Wang, E-mail: 460532929com and Xu Zhang, E-mail: 1990486976com


Received 2018-6-30
Accepted 2018-10-24
Published 2019-1-1