MicroRNA binding site polymorphisms as biomarkers in cancer management and research
- PMID: 25114582
- PMCID: PMC4126202
- DOI: 10.2147/PGPM.S61693
MicroRNA binding site polymorphisms as biomarkers in cancer management and research
Abstract
MicroRNAs (miRNAs) are important regulators of eukaryotic gene expression. They have been implicated in a broad range of biological processes, and miRNA-related genetic alterations probably underlie several human diseases. Single nucleotide polymorphisms of transcripts may modulate the posttranscriptional regulation of gene expression by miRNAs and explain interindividual variability in cancer risk and in chemotherapy response. On the basis of recent association studies published in the literature, the present review mainly summarizes the potential role of miRNAs as molecular biomarkers for disease susceptibility, diagnosis, prognosis, and drug-response prediction in tumors. Many clues suggest a role for polymorphisms within the 3' untranslated regions of KRAS rs61764370, SET8 rs16917496, and MDM4 rs4245739 as SNPs in miRNA binding sites highly promising in the biology of human cancer. However, more studies are needed to better characterize the composite spectrum of genetic determinants for future use of markers in risk prediction and clinical management of diseases, heading toward personalized medicine.
Keywords: 3′-UTR target binding site; biomarkers; cancer risk; miRSNP.
Similar articles
-
Prognostic value of microRNA 502 binding site SNP in the 3'-untranslated region of the SET8 gene in patients with non-Hodgkin's lymphoma.Tumori. 2014 Sep-Oct;100(5):553-8. doi: 10.1700/1660.18180. Tumori. 2014. PMID: 25343552
-
Type 2 diabetes mellitus-related genetic polymorphisms in microRNAs and microRNA target sites.J Diabetes. 2014 Jul;6(4):279-89. doi: 10.1111/1753-0407.12143. Epub 2014 Apr 15. J Diabetes. 2014. PMID: 24606011 Review.
-
Variations within 3'-UTR of MDM4 gene contribute to clinical outcomes of advanced non-small cell lung cancer patients following platinum-based chemotherapy.Oncotarget. 2017 Mar 7;8(10):16313-16324. doi: 10.18632/oncotarget.10771. Oncotarget. 2017. PMID: 27462918 Free PMC article.
-
MicroRNA binding site polymorphisms as biomarkers of cancer risk.Expert Rev Mol Diagn. 2010 Sep;10(6):817-29. doi: 10.1586/erm.10.59. Expert Rev Mol Diagn. 2010. PMID: 20843204 Free PMC article.
-
MicroRNA polymorphisms as markers of risk, prognosis and treatment response in hematological malignancies.Crit Rev Oncol Hematol. 2015 Jan;93(1):1-17. doi: 10.1016/j.critrevonc.2014.08.006. Epub 2014 Sep 2. Crit Rev Oncol Hematol. 2015. PMID: 25217091 Review.
Cited by
-
The KRAS-variant and its impact on normal breast epithelial cell biology.Cell Death Differ. 2019 Dec;26(12):2568-2576. doi: 10.1038/s41418-019-0320-y. Epub 2019 Apr 1. Cell Death Differ. 2019. PMID: 30932013 Free PMC article.
-
Impact of MICA 3'UTR allelic variability on miRNA binding prediction, a bioinformatic approach.Front Genet. 2023 Dec 7;14:1273296. doi: 10.3389/fgene.2023.1273296. eCollection 2023. Front Genet. 2023. PMID: 38146340 Free PMC article.
-
Dysregulated MicroRNA Expression Profiles and Potential Cellular, Circulating and Polymorphic Biomarkers in Non-Hodgkin Lymphoma.Genes (Basel). 2016 Dec 17;7(12):130. doi: 10.3390/genes7120130. Genes (Basel). 2016. PMID: 27999330 Free PMC article. Review.
-
Functional microRNA binding site variants.Mol Oncol. 2019 Jan;13(1):4-8. doi: 10.1002/1878-0261.12421. Epub 2018 Dec 26. Mol Oncol. 2019. PMID: 30536617 Free PMC article. Review.
-
Estrogen withdrawal, increased breast cancer risk and the KRAS-variant.Cell Cycle. 2015;14(13):2091-9. doi: 10.1080/15384101.2015.1041694. Epub 2015 May 11. Cell Cycle. 2015. PMID: 25961464 Free PMC article.
References
Publication types
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous