| Literature DB >> 33446698 |
Tao Peng1, Yangyang Sun2, Zhiwei Lv3, Ze Zhang3, Quanxin Su3, Hao Wu3, Wei Zhang4, Wei Yuan5, Li Zuo3, Li Shi3, Li-Feng Zhang6, Xiaoli Zhou7, Yuanyuan Mi8.
Abstract
The correlation between G388R or V10I polymorphisms of fibroblast growth factor receptor (FGFR) 4 gene and the risk of carcinoma has been investigated previously, but the results are contradictory. Odds ratios (ORs) with 95% confidence intervals (95%CIs), in silico tools, and immunohistochemical staining (IHS) were adopted to assess the association. In total, 13,793 cancer patients and 16,179 controls were evaluated in our pooled analysis. Summarization of all the studies showed that G388R polymorphism is associated with elevated susceptibility to cancer under homozygous comparison (OR = 1.21, 95%CI = 1.03-1.43, P = 0.020) and a recessive genetic model (OR = 1.21, 95%CI = 1.04-1.41, P = 0.012). In the stratification analysis by cancer type and ethnicity, similar findings were indicated for prostate cancer, breast cancer, and individuals of Asian descendant. Polyphen2 bioinformatics analysis showed that the G388R mutation is predicted to damage the protein function of FGFR4. IHS analysis indicated that FGFR4 expression is increased in advanced prostate cancer. These findings may guide personalized treatment of certain types of cancers. Up-regulation of FGFR4 may be related to a poor prognosis in prostate cancer.Entities:
Year: 2021 PMID: 33446698 PMCID: PMC7809464 DOI: 10.1038/s41598-020-80146-y
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379