PSCA rs2294008 C > T polymorphism contributes to gastric and bladder cancer risk

Abstract

Background

Previous studies suggested genetic variations in PSCA (prostate stem cell antigen) may confer the susceptibility of cancer. Many case–control studies have reported the relationship between PSCA rs2294008 C > T polymorphism and cancer, especially gastric cancer and bladder cancer. However, the results are inconsistent. This meta-analysis is aimed at evaluating the association of rs2294008 polymorphism with cancer risk.

Methods

The databases of PubMed, ISI Web of Knowledge, EMBASE, and Chinese National Knowledge Infrastructure (CNKI) were searched for related publications. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to estimate the strength of the associations. Fixed models were used when heterogeneity among studies was not detected, otherwise the random model was used.

Results

Twenty-six studies from 24 articles with 30,050 multiple cancer cases and 51,670 controls were pooled into this meta-analysis. The results showed that the rs2294008 polymorphism was associated with increased cancer risk in any genetic model (T vs C, OR: 1.18, 95% CI: 1.08–1.28; TT vs CC, OR: 1.36, 95% CI: 1.14–1.62; TC vs CC, OR: 1.29, 95% CI: 1.17–1.44; TT + TC vs CC, OR: 1.32, 95% CI: 1.18–1.49; TT vs TC + CC, OR: 1.15, 95% CI: 1.02–1.30). In stratified analysis by cancer type, we found that the T allele had a significant high risk of gastric and bladder cancer, but not in other cancers. In subgroup analysis by ethnicity, increased cancer risk was found in both Asians and Caucasians.

Conclusion

Our study suggested that the PSCA rs2294008 C > T polymorphism is a risk factor for cancer, especially in gastric and bladder cancer.

Introduction

Cancer has become one of the most serious diseases threatening human health. According data from GLOBOCAN 2008, about 12.7 million new cancer cases and 7.6 million cancer deaths have occurred.1 Unfortunately, the mechanisms of cancer still need intensive study. Interactions between genetic and environmental factors were proved to play a dominant role in the occurrence and progression of cancer.2,3 It seems that discovering the effects of genes and the environment on humans would result in a big step being taken toward healing cancer.

Prostate stem cell antigen (PSCA) is a prostate-specific gene, which was initially discovered by Reiter et al by representational difference analysis.4 PSCA encodes a 123 amino acid cell surface protein with 30% homology to stem cell antigen 2 (SCA-2) that belongs to the Thy-1/Ly-6 family and is located on chromosome 8q24.2. PSCA is not only overexpressed in prostate cancer, but was also demonstrated to be highly expressed in other malignancies such as bladder, renal, pancreatic, and ovarian cancers.4–8 The most extensively studied single nucleotide polymorphism (SNP) in PSCA is rs2294008 C > T. Although in vitro experiments have revealed that the variant rs2294008T could reduce the transcriptional activity of an upstream fragment of PSCA, its mechanism and physiological function are still unknown.5,9 Previously, genome-wide association studies (GWAS) have found that the rs2294008 polymorphism in PSCA is significantly associated with gastric and bladder cancers. Although several studies have described the relationship between the rs2294008 polymorphism and other cancers, the sample sizes of these studies were small. More recently, five meta-analyses have assessed the relationship between the polymorphism of PSCA rs2294008 C > T and the susceptibility to gastric cancer.10–14 However, the results of these meta-analyses were not entirely consistent. Especially the results of subgroup analysis by ethnicity are controversial. Furthermore, there is a lack of evidence of a relationship between the rs2294008 polymorphism and cancer overall. Additionally, the genetic variant of rs2294008 may be correlated with cancer risk in different cancer type and/or ethnicity. Herein, we carried out a meta-analysis to derive a more precise evaluation on the relationship between the rs2294008 polymorphism and cancer risk.

Materials and methods

Publication search strategy

We searched the databases of PubMed, ISI Web of Knowledge, EMBASE, and Chinese National Knowledge Infrastructure (CNKI) for related articles with the keywords: “PSCA/Prostate stem cell antigen”, “rs2294008”, “single nucleotide polymorphism/SNP/variation/genotype”, and “cancer/carcinoma/tumor/neoplasm”. The last search was updated on September 30, 2014. All published papers with available full text matching the eligible criteria were retrieved. Furthermore, the references of relevant reviews and eligible articles that our search retrieved were checked.

Inclusion and exclusion criteria

The following criteria were used to select the eligible literature for this meta-analysis: 1) original papers investigating the associations between PSCA (rs2294008) polymorphisms and cancer risk; 2) case–control studies; and 3) full-text published articles and included detailed genotyping data.

Accordingly, the exclusion criteria were: 1) no control group; 2) no available or detailed genotype frequency; and 3) reviews and duplicated studies.

Data extraction and synthesis

The literature were carefully extracted from all eligible studies independently by two reviewers according to the inclusion and exclusion criteria mentioned above. If these two reviewers could not reach an agreement, another reviewer was consulted to resolve the controversy. The following information were extracted from all included studies: first author, published year, country of origin, cancer type, ethnicity, genotyping methods, source of control, sample size of cases and controls, and the distribution of each genotype in case and control groups. The subgroups grouped according to cancer types included gastric cancer, bladder cancer, and others. With regard to ethnicity, the studies included Caucasian, Asian, and mixed ethnicity (ie, the ethnicity was unclear).

Statistical analysis

The associations between the PSCA (rs2294008) polymorphism and cancer risk were measured by the odds ratio (OR) with 95% confidence intervals (CIs) according to allele contrast (T vs C), homozygote (TT vs CC), heterozygote (TC vs CC), recessive (TT vs CC + TC), and dominant (CC vs TC + TT) models. The significance of the overall OR was determined by the Z test. Heterogeneity among studies was evaluated with the Q and I² statistic tests. If the P-value of the heterogeneity test was greater than 0.05 (P>0.05), the pooled OR estimate of each study was calculated by the fixed effects model. Otherwise, the random effects model was used.15 Furthermore, sources of heterogeneity were investigated by stratified analysis based on cancer type and ethnicity as mentioned above. A funnel plot was used to evaluate publication bias. All statistical analyses were carried out with Review Manager (Revman; v5.2; The Cochrane Collaboration, Oxford, UK).

Results

Characteristics of studies

As shown in Figure 1, a total of 38 potential articles were extracted after the initial search. Fourteen articles were excluded after further screening. Six studies were excluded because they were systematic review articles. One article was excluded because it was not a case–control study. Seven articles were excluded because of a lack of detailed genotyping data. Finally, 26 studies from 24 publications9,16–38 including 30,050 multiple cancer cases and 51,670 controls were included in this meta-analysis.

Figure 1.

Flow chart of study selection.

Abbreviation: CNKI, Chinese National Knowledge Infrastructure.

The characteristics of the included studies are summarized in Table 1. Among the 26 studies, there were 17 studies of gastric cancer, five studies of bladder cancer, two studies of esophageal cancer, two studies of gallbladder cancer, and one study of colorectal cancer. As for subjects, 19 studies had an Asian background, seven studies had a Caucasian background, and only one had a ‘mixed’ background. Furthermore, there were eleven hospital-based studies and 15 population-based studies.

Table 1.

Characteristics of studies included in the meta-analysis

Study	Year	Country	Ethnicity	Study design	Genotyping method	Source of control	Cancer type	Sample size (case/control)
Dai et al16	2014	People’s Republic of China	Asian	CC	TaqMan	Population	EC	2,083/2,220
Wang et al17	2014	People’s Republic of China	Asian	CC	TaqMan	Population	BC	1,210/1,008
Ma et al18	2013	People’s Republic of China	Asian	CC	iPLEX	Population	BC	184/962
Zhao et al19	2013	People’s Republic of China	Asian	CC	DHPLC	Population	GC	717/951
Rizzato et al20	2013	Venezuela	Mixed	CC	TaqMan	Hospital	GC	180/1,061
Rai et al21	2013	India	Asian	CC	TaqMan	Population	GBC	405/247
Ono et al22	2013	Japan	Asian	CC	TaqMan	Hospital	GBC	44/173
Fu et al23	2012	Europe	Caucasian	CC	TaqMan	Population	BC	5,393/7,324
Li et al24	2012	People’s Republic of China	Asian	CC	iPLEX	Hospital	GC	300/300
Smith et al25	2012	Scotland	Caucasian	CC	TaqMan	Hospital	CRC	77/804
Sala et al26	2012	Europe	Caucasian	CC	SNP array	Population	GC	411/1,530
Zhao et al27	2012	People’s Republic of China	Asian	CC	DHPLC	Population	GC	185/200
Tanikawa et al28	2012	Japan	Asian	CC	SNP array	Hospital	GC	2,300/16,567
Song et al29	2011	Korea	Asian	CC	PCR-RFLP	Hospital	GC	3,245/1,700
Zeng et al30	2011	People’s Republic of China	Asian	CC	PCR-RFLP	Hospital	GC	460/549
Lochhead et al31a	2011	Poland	Caucasian	CC	TaqMan	Population	GC	312/383
Lochhead et al31b	2011	USA	Caucasian	CC	TaqMan	Population	Upper GIC	468*/211
Wang et al32	2010	People’s Republic of China	Asian	CC	PCR-RFLP	Hospital	BC	581/580
Ou et al33	2010	People’s Republic of China	Asian	CC	PCR/LDR	Hospital	GC	196/246
Lu et al34	2010	People’s Republic of China	Asian	CC	PCR-RFLP	Population	GC	1,053/1,100
Chen et al35	2010	People’s Republic of China	Asian	CC	PCR-RFLP	Hospital	GC	460/549
Wu et al36	2009	Europe	Caucasian	CC	TaqMan	Population	BC	5,038/9,363
Matsuo et al37	2009	Japan	Asian	CC	TaqMan	Hospital	GC	708/708
Wu et al38	2009	People’s Republic of China	Asian	CC	PCR-RFLP	Population	GC	1,736/1,020
Sakamoto et al9a	2008	Japan	Asian	CC	TaqMan	Population	GC	1,531/1,399
Sakamoto et al9b	2008	Korea	Asian	CC	TaqMan	Population	GC	871/390

Notes:

^*Including 309 gastric cancer cases and 159 esophageal cancer cases. Lochhead et al31a refers the study evaluated association of the rs2294008 polymorphism with gastric cancer risk and Lochhead et al31b refers to the study evaluated association of the rs2294008 polymorphism with upper GI cancer risk. Sakamoto et al9a refers to the study evaluated association of the rs2294008 with gastric cancer types in Japan and Sakamoto et al9b refers to the study evaluated association of the rs2294008 with gastric cancer types in Korea.

Abbreviations: BC, bladder cancer; CC, case–control; CRC, colorectal cancer; DHPLC, denaturing high-performance liquid chromatography; EC, esophageal cancer; GBC, gallbladder cancer; GIC, gastrointestinal cancers; GC, gastric cancer; LDR, ligation detection reaction; PCR, polymerase chain reaction; RFLP, restriction fragment length polymorphism; SNP, single nucleotide polymorphism.

Quantitative data synthesis

As shown in Table 2, the frequency of the minor allele varied widely across the 26 eligible studies, ranging from 0.23 to 0.71. The average frequency of the minor allele in gastric cancer, bladder cancer, and other cancers were 0.45, 0.47, and 0.27, respectively. The average frequency of the T allele was 0.40, 0.49, and 0.63 in Asians, Caucasians, and the mixed group, respectively.

Table 2.

PSCA rs2294008 polymorphism genotype distribution and allele frequency in cases and controls

Study	Genotype (N)								Allele frequency (N)				MAF
	Case				Control				Case		Control
	Total	CC	CT	TT	Total	CC	CT	TT	C	T	C	T
Gastric cancer
Zhao et al19	717	275	342	100	951	465	401	85	892	542	1,331	571	0.38
Rizzato et al20	180	23	86	69	1,061	231	507	319	132	224	969	1,145	0.63
Li et al24	300	124	141	35	300	168	111	21	389	211	447	153	0.35
Sala et al26	411	93	198	118	1,530	491	714	310	384	434	1,696	1,334	0.53
Zhao et al27	185	74	90	21	200	108	79	13	238	132	295	105	0.37
Tanikawa et al28	2,300	1,030	1,073	197	16,567	6,620	7,587	2,360	3,133	1,467	20,827	12,307	0.32
Song et al29	3,245	576	1,620	1,049	1,700	414	818	468	2,772	3,718	1,646	1,754	0.57
Zeng et al30	460	202	216	42	549	289	223	37	620	300	801	297	0.33
Lochhead et al I31	312	47	143	102	383	101	166	115	237	347	368	396	0.59
Lochhead et al II31	309	85	129	94	211	49	110	49	299	317	208	208	0.51
Ou et al33	196	85	93	18	246	132	96	18	263	129	360	132	0.33
Lu et al34	1,053	547	404	72	1,110	605	387	77	1,498	548	1,597	541	0.27
Chen et al35	460	202	216	42	549	289	223	37	620	300	801	297	0.33
Matsuo et al37	708	330	329	49	708	273	338	97	989	427	884	532	0.30
Wu et al38	1,736	759	819	132	1,020	506	412	77	2,337	1,083	1,424	566	0.32
Sakamoto et al I9	1,531	96	700	728	1,399	210	650	536	892	2,156	1,070	1,722	0.71
Sakamoto et al II9	871	133	461	277	390	122	176	92	727	1,015	420	360	0.58
Bladder cancer
Wang et al17	1,210	604	509	97	1,008	566	376	66	1,717	703	1,508	508	0.29
Ma et al18	184	84	80	11	962	543	355	64	248	102	1,441	483	0.29
Fu et al23	5,393	1,363	2,804	1,226	7,324	2,107	3,645	1,572	5,530	5,256	7,859	6,789	0.49
Wang et al32	581	272	259	50	580	316	220	44	803	359	852	308	0.31
Wu et al36	5,038	1,288	2,613	1,137	9,363	2,842	4,668	1,853	5,189	4,887	10,352	8,374	0.49
Other cancers
Esophageal cancer
Dai et al16	2,083	1,232	724	127	2,220	1,222	851	147	3,188	978	3,295	1,145	0.23
Lochhead et al II31	159	61	63	34	211	49	110	49	185	131	208	208	0.41
Gallbladder cancer
Rai et al21	405	104	233	68	247	79	126	42	441	369	284	210	0.46
Ono et al22	44	12	23	9	173	68	75	30	47	41	211	135	0.47
Colorectal cancer
Smith et al25	77	25	39	13	804	287	387	130	89	65	961	647	0.42

Notes: C represents the major allele, T represents the minor allele.

Abbreviation: MAF, minor allele frequencies; M–H, Mantel–Haenszel.

In terms of overall analysis, a significant association was found in all genetic models (T vs C, OR: 1.18, 95% CI: 1.08–1.28, P=0.0001; TT vs CC, OR: 1.36, 95% CI: 1.14–1.62, P=0.0008; TC vs CC, OR: 1.29, 95% CI: 1.17–1.44, P<0.00001; dominant model TT + TC vs CC, OR: 1.32, 95% CI: 1.18–1.49, P<0.00001; recessive model TT vs TC + CC, OR: 1.15, 95% CI: 1.02–1.30, P=0.02).

In subgroup analysis by cancer type, we found that the T allele had a significantly high risk of gastric cancer and bladder cancer, but null association in other cancers (Table 3). For gastric cancer, our meta-analysis contained 17 studies with 14,886 cases and 28,782 controls. The rs2294008 polymorphism was associated with gastric cancer risk in four genetic models (T vs C, OR: 1.26, 95% CI: 1.10–1.45, P=0.001; TT vs CC, OR: 1.51, 95% CI: 1.10–2.08, P=0.01; TC vs CC, OR: 1.39, 95% CI: 1.19–1.63, P<0.0001; TT + TC vs CC, OR: 1.44, 95% CI: 1.19–1.74, P=0.0002). However, the recessive model showed that there was no association between rs2294008 and gastric cancer (OR: 1.22, 95% CI: 0.99–1.49, P=0.06).

Table 3.

Meta-analysis results

Comparisons	OR	95% CI	P-value	Heterogeneity		Effects model
				I2	P-value
T vs C	1.18	1.08–1.28	0.0001	91%	<0.00001	R
Gastric cancer	1.26	1.10–1.45	0.001	94%	<0.00001	R
Bladder cancer	1.13	1.06–1.21	0.0005	63%	0.03	R
Others	0.97	0.81–1.16	0.75	62%	0.03	R
Asian	1.19	1.05–1.35	0.007	93%	<0.00001	R
Caucasian	1.15	1.04–1.26	0.004	75%	0.0005	R
Mixed	1.44	1.14–1.81	0.002	NA	NA
TT vs CC	1.36	1.14–1.62	0.0008	90%	<0.00001	R
Gastric cancer	1.51	1.10–2.08	0.01	94%	<0.00001	R
Bladder cancer	1.28	1.20–1.37	<0.00001	0%	0.57	F
Others	0.91	0.75–1.10	0.33	39%	0.16	F
Asian	1.37	1.03–1.82	0.03	92%	<0.00001	R
Caucasian	1.32	1.10–1.59	0.003	73%	0.001	R
Mixed	2.17	1.32–3.59	0.002	NA	NA
TC vs CC	1.29	1.17–1.44	<0.00001	85%	<0.00001	R
Gastric cancer	1.39	1.19–1.63	<0.0001	87%	<0.00001	R
Bladder cancer	1.23	1.17–1.30	<0.00001	0%	0.65	F
Others	0.98	0.68–1.41	0.90	77%	0.001	R
Asian	1.36	1.18–1.57	<0.0001	88%	<0.00001	R
Caucasian	1.13	0.95–1.34	0.16	79%	<0.0001	R
Mixed	1.70	1.05–2.77	0.03	NA	NA
TT + TC vs CC	1.32	1.18–1.49	<0.00001	90%	<0.00001	R
Gastric cancer	1.44	1.19–1.74	0.0002	92%	<0.00001	R
Bladder cancer	1.25	1.19–1.31	<0.00001	0%	0.64	F
Others	0.98	0.69–1.38	0.90	77%	0.002	R
Asian	1.38	1.17–1.62	0.0001	92%	<0.00001	R
Caucasian	1.18	1.00–1.40	0.05	80%	<0.0001	R
Mixed	1.88	1.19–2.99	0.007	NA	NA
TT vs CC + TC	1.15	1.02–1.30	0.02	83%	<0.00001	R
Gastric cancer	1.22	0.99–1.49	0.06	89%	<0.00001	R
Bladder cancer	1.13	1.07–1.20	<0.0001	0%	0.56	F
Others	0.95	0.79–1.14	0.57	0%	0.96	F
Asian	1.13	0.93–1.36	0.87	87%	<0.00001	R
Caucasian	1.15	1.09–1.22	<0.00001	47%	0.08	F
Mixed	1.46	1.05–2.03	0.02	NA	NA

Note: P-values in bold indicate nonsignificance.

Abbreviations: F, fixed; NA, not applicable; R, random; CI, confidence interval; OR, odds ratio; M–H, Mantel–Haenszel.

Five studies with 12,397 cases and 19,237 controls were used to evaluate the relationship between the rs2294008 polymorphism and bladder cancer risk. As shown in Table 3 and Figure 2, there was a significant association between rs2294008 and bladder cancer risk in all genetic models (T vs C, OR: 1.13, 95% CI: 1.06–1.21, P=0.0005; TT vs CC, OR: 1.28, 95% CI: 1.20–1.37, P<0.00001; TC vs CC, OR: 1.23, 95% CI: 1.17–1.30, P<0.00001; TT +TC vs CC, OR: 1.25, 95% CI: 1.19–1.31, P<0.00001; TT vs TC + CC, OR: 1.13, 95% CI: 1.07–1.20, P<0.0001).

Figure 2.

Forest plots of the PSCA rs2294008 polymorphism and cancer risk in the overall population and each subgroup stratified by cancer type (T vs C).

Notes: The squares and horizontal lines correspond to the study-specific OR and 95% CI. The area of the squares reflects the weight (inverse of the variance). The diamonds represent the summary OR and 95% CI.

Abbreviations: CI, confidence interval; OR, odds ratio; GC, gastric cancer; BC, bladder cancer; M–H, Mantel–Haenszel.

In the stratified analysis by ethnicity, pooled analysis of Asians showed that the T allele of the PSCA rs2294008 polymorphism was associated with increased cancer risk under all genetic models except for the recessive model (T vs C, OR: 1.19, 95% CI: 1.05–1.35, P=0.007, Figure 3; TT vs CC, OR: 1.37, 95% CI: 1.03–1.82, P=0.03; TC vs CC, OR: 1.36, 95% CI: 1.18–1.57, P<0.0001; TT + TC vs CC, OR: 1.38, 95% CI: 1.17–1.62, P=0.0001). PSCA rs2294008 showed a significant association among Caucasians based on three models (T vs C, OR: 1.15, 95% CI: 1.04–1.26, P=0.004, Figure 3; TT vs CC, OR: 1.32, 95% CI: 1.10–1.59, P=0.003; TT vs TC + CC, OR: 1.15, 95% CI: 1.09–1.22, P<0.00001). However, there was no significant association in Caucasians in the other two genetic models (TC vs CC, OR: 1.13, 95% CI: 0.95–1.34; TT + TC vs CC, OR: 1.18, 95% CI: 1.00–1.40).

Figure 3.

Forest plots of PSCA rs2294008 polymorphism and cancer risk in the overall population and each subgroup stratified by ethnicity (T vs C).

Notes: The squares and horizontal lines correspond to the study specific OR and 95% CI. The area of the squares reflects the weight (inverse of the variance). The diamonds represent the summary OR and 95% CI.

Abbreviations: CI, confidence interval; OR, odds ratio; M–H, Mantel–Haenszel.

Tests of heterogeneity

The Q and I² statistic tests were used to evaluate heterogeneity. For the overall studies, there was statistically significant heterogeneity in this meta-analysis (T vs C, P<0.00001, I²=91%; TT vs CC, P<0.00001, I²=90%; TC vs CC, P<0.00001, I²=85%; dominant model TT + TC vs CC, P<0.00001, I²=90%; recessive model TT vs CC + TC, P<0.00001, I²=83%). Therefore, we carried on further subgroup analyses by cancer type and ethnicity, respectively. When the P-value of the heterogeneity test was more than 0.05 (P>0.05) in the following analyses, a fixed effects model was performed. Otherwise, the random effects model was used (shown in Table 3).

Publication bias

A funnel plot was used performed to evaluate publication bias in this meta-analysis. According to the funnel plot generated for the genetic models, there was an absence of obvious asymmetries for the distributions of ORs from every study (Figure 4). Therefore, the results indicated that publication bias had little effect in this meta-analysis.

Figure 4.

Funnel plot assessing evidence of publication bias from 26 studies (T vs C).

Abbreviations: OR, odds ratio; SE, standard error.

Discussion

PSCA is a member of the Thy-1/Ly-6 family of glycosylphosphatidylinositol (GPI)-anchored surface proteins, comprising three exons and two introns. Proteins in the Thy-1 family and GPI-anchored proteins have been proven to play a role in T cell activation.39 It has been demonstrated to be upregulated in prostate cancer and several other tumors and plays an important role in cell adhesion, proliferation, and survival.11 Recently, many cancer GWAS and replication studies have revealed the relationship between PSCA and risk of different cancers. A study performed by Sakamoto et al indicated that the mechanism of PSCA-suppressing cancers may be involved in cell proliferation inhibition and/or cell death induction.9 The findings of our meta-analysis may demonstrate that rs2294008 acts as an effect modifier in the development of different cancers. Of course, further biologically functional studies are warranted to verify the molecular mechanisms.

This comprehensive meta-analysis, involving 26 studies from 24 articles with 30,050 multiple cancer cases and 51,671 controls, showed that the rs2294008 polymorphism is significantly associated with overall cancer risk based on all genetic models. Further stratified analyses by cancer type revealed that the polymorphism was associated with an increased risk for gastric and bladder cancer; no association was found with other cancers in all genetic models. Studies from Dai et al16 and Lochhead et al31 indicated that the variant rs2294008C may have a protective role in esophageal cancer, but large well-designed studies are warranted to confirm this conclusion. The stratified analysis by ethnicity showed that the rs2294008 polymorphism was associated with an increased risk of cancer in both Asians and Caucasians. However, there was no study based on patients with an African background. Larger scale multicenter studies based on Africans are warranted to further validate the association between the rs2294008 polymorphism and cancer risk.

So far, there have been five meta-analyses that have investigated the role of the PSCA rs2294008 polymorphism in gastric cancer risk.10–14 All of them had the same finding that the rs2294008 polymorphism is associated with increased risk of gastric cancer. The stratified analyses by ethnicity were performed in four meta-analyses.10–12,14 Significantly increased risks were found for rs2294008 both among Asians and Caucasians in three articles,10–12 which is congruous with our results. However, one study showed no significant associations with the rs2294008 polymorphism and Caucasians.14 The latest research in these five published meta-analyses was performed by Gu et al.14 Their last search update was on August 2013, and in total, they identified 16 studies, including 18,820 gastric cases and 35,756 controls for the rs2294008 polymorphism. Compared to these five meta-analyses, we added another nine studies on other cancers in addition to gastric cancer. Our updated meta-analysis extracted data from all the published studies including 26 studies from 24 articles with 30,050 cancer cases and 51,671 controls. This meta-analysis provided evidence on the overall cancer risk of rs2294008 and contained the newest data and largest sample size on the relationship between rs2294008 and cancer. Thus, our results are more comprehensive and persuasive.

Although the pooled analysis was performed to show the association between rs2294008 and cancer risk, some limitations still inevitably exist in this meta-analysis. Firstly, we excluded some studies because of the limits of raw data. Secondly, we could not obtain all articles. Some unpublished literature and relevant published reports in other languages except English and Chinese that may be eligible for this meta-analysis were missed. Thirdly, there were only two studies on esophageal cancer, two on gallbladder cancer, and one on colorectal cancer. Additionally, there was a lack of studies on other types of cancers. Hence, the final OR was largely contributed by the ORs of gastric or bladder cancer; more evidence is needed to prove whether the rs2294008 polymorphism is association with cancer overall. Further large-scale multicenter studies based on a variety of cancer types are needed. Fourthly, the sources of the controls were not consistent. Both population-based healthy individuals and hospital patients without cancer were included in the control groups. Controls enrolled from hospitals may not always truly represent the underlying source populations, especially when the polymorphism was also expected to affect the risk of other diseases. Fifthly, the genotyping methods of the eligible studies were not identical, which may influence the results. Finally, because of the limit of individual data, the ORs of this meta-analysis were not strictly adjusted by the same potential confounders, such as age, sex, and stage of tumor. Additionally, a more precise analysis could be performed to eliminate the confounding bias.

Conclusion

In conclusion, the present meta-analysis demonstrated that the PSCA rs2294008 C > T polymorphism is a risk factor for cancer in both Asians and Caucasians. Furthermore, rs2294008 is associated with an increased risk of gastric and bladder cancer. Further large case–control studies are needed to assess the relationship between rs2294008 and other cancer types.