Urinary Bladder Cancer Susceptibility Markers. What Do We Know about Functional Mechanisms?

被引:25
作者
Dudek, Aleksandra M. [1 ,2 ,3 ]
Grotenhuis, Anne J. [2 ,4 ]
Vermeulen, Sita H. [2 ,4 ]
Kiemeney, Lambertus A. L. M. [1 ,2 ,4 ]
Verhaegh, Gerald W. [1 ,3 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Urol, NL-6525 GA Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Hlth Evidence, NL-6525 EZ Nijmegen, Netherlands
[3] Nijmegen Ctr Mol Life Sci, NL-6525 GA Nijmegen, Netherlands
[4] Nijmegen Ctr Evidence Based Practice, NL-6525 GA Nijmegen, Netherlands
关键词
bladder cancer; GWAS; risk variants; GENOME-WIDE ASSOCIATION; STEM-CELL ANTIGEN; COMMON GENETIC-VARIANTS; HUMAN UDP-GLUCURONOSYLTRANSFERASES; TERT PROMOTER MUTATIONS; LONG-RANGE INTERACTION; TUMOR-SUPPRESSOR GENE; TELOMERE LENGTH; CONFERS SUSCEPTIBILITY; 8Q24; PROSTATE;
D O I
10.3390/ijms140612346
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genome-wide association studies (GWAS) have been successful in the identification of the several urinary bladder cancer (UBC) susceptibility loci, pointing towards novel genes involved in tumor development. Despite that, functional characterization of the identified variants remains challenging, as they mostly map to poorly understood, non-coding regions. Recently, two of the UBC risk variants (PSCA and UGT1A) were confirmed to have functional consequences. They were shown to modify bladder cancer risk by influencing gene expression in an allele-specific manner. Although the role of the other UBC risk variants is unknown, it can be hypothesized-based on studies from different cancer types-that they influence cancer susceptibility by alterations in regulatory networks. The insight into UBC heritability gained through GWAS and further functional studies can impact on cancer prevention and screening, as well as on the development of new biomarkers and future personalized therapies.
引用
收藏
页码:12346 / 12366
页数:21
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