Dopamine receptor D2 genetic variations is associated with the risk and clinicopathological variables of urothelial cell carcinoma in a Taiwanese population

被引:8
|
作者
Tung, Min-Che [1 ,2 ]
Wen, Yu-Ching [3 ,4 ]
Wang, Shian-Shiang [5 ,6 ,7 ]
Lin, Yung-Wei [3 ,4 ]
Liu, Yu-Cheng [1 ,2 ]
Yang, Shun-Fa [7 ,8 ]
Chien, Ming-Hsien [1 ,9 ]
机构
[1] Taipei Med Univ, Coll Med, Grad Inst Clin Med, Taipei, Taiwan
[2] TungsTaichung Metro Harbor Hosp, Dept Surg, Taichung, Taiwan
[3] Taipei Med Univ, Wan Fang Hosp, Dept Urol, Taipei, Taiwan
[4] Taipei Med Univ, Coll Med, Sch Med, Dept Urol, Taipei, Taiwan
[5] Taichung Vet Gen Hosp, Dept Surg, Div Urol, Taichung, Taiwan
[6] Chung Shan Med Univ, Sch Med, Taichung, Taiwan
[7] Chung Shan Med Univ, Inst Med, 110 Chien Kuo N Rd,Sect 1, Taichung 402, Taiwan
[8] Chung Shan Med Univ Hosp, Dept Med Res, Taichung, Taiwan
[9] Taipei Med Univ, Wan Fang Hosp, Dept Med Educ & Res, Taipei, Taiwan
来源
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES | 2018年 / 15卷 / 11期
关键词
Dopamine receptor D2 gene; Polymorphism; Susceptibility; Clinicopathologic development; Urothelial cell carcinoma; BLADDER-CANCER; POLYMORPHISMS; DRD2; IDENTIFICATION; METAANALYSIS; RECURRENCE; MUTATIONS; SMOKING; BINDING;
D O I
10.7150/ijms.26895
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dopamine receptor D2 (DRD2) is overexpressed in several kinds of cancers and was correlated with the prognosis of these cancers. Polymorphisms within the DRD2 gene were shown to be associated with lung and colon cancers. The purpose of this study was to explore effects of DRD2 gene polymorphisms on the susceptibility to and clinicopathological characteristics of urothelial cell carcinoma (UCC). In total, 369 patients diagnosed with UCC and 738 healthy controls were enrolled to analyze DRD2 genotypes at four loci (rs1799732, -141C>del; rs1079597, TaqIB; rs6277, 957C>T; and rs1800497, TaqIA) using a TaqMan-based real-time polymerase chain reaction (PCR). We found a significantly lower risk for UCC in individuals with the DRD2 rs6277 CT genotype compared to those with the wild-type CC genotype (adjusted odds ratio (AOR)=0.405, 95% confidence interval (CI): 0.196 similar to 0.837, p=0.015). In 124 younger patients (aged < 65 years) of the recruited UCC cohort, patients who carried at least one T allele of DRD2 rs1800497 were at higher risk (AOR=2.270, 95% CI: 1.060 similar to 4.860, p=0.033) of developing an invasive stage (pT2 similar to pT4). In 128 female patients of the recruited UCC cohort, patients who carried at least one deletion allele of DRD2 rs1799732 showed a higher incidence of having an invasive stage (AOR=2.585, 95% CI: 1.066 similar to 6.264, p=0.032) and a large tumor (AOR=2.778, 95% CI: 1.146 similar to 6.735, p=0.021). Further analyses of The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) datasets revealed correlations of the expression of DRD2 with an invasive tumor, tumor metastasis, and the lower survival rate in patients with UCC. Our findings suggest that DRD2 levels might affect the progression of UCC, and the polymorphisms rs6277, rs1800497, and rs1799732 of DRD2 are probably associated with the susceptibility and clinicopathologic development of UCC in a Taiwanese population.
引用
收藏
页码:1187 / 1193
页数:7
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