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Functional micro RNA binding site variants
Author(s) -
Yuan Ye,
Weidhaas Joanne B.
Publication year - 2019
Publication title -
molecular oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.332
H-Index - 88
eISSN - 1878-0261
pISSN - 1574-7891
DOI - 10.1002/1878-0261.12421
Subject(s) - biology , nonsynonymous substitution , single nucleotide polymorphism , snp , genetics , carcinogenesis , rna , gene , microrna , computational biology , genome , genotype
Germline single nucleotide polymorphisms are one of the most common genetic variations. Polymorphisms that cause nonsynonymous mutations in gene coding regions are known to cause serious deleterious downstream effects. However, even polymorphisms in noncoding regions can have profound functional consequences by disrupting essential regulatory sites. Specifically, polymorphisms that alter micro RNA binding sites can disrupt the regulation of hallmark biological pathways implicated in tumorigenesis and tumor progression. Many of these micro RNA ‐associated polymorphisms (miR‐ SNP s) have recently been shown to be important biomarkers of cancer risk, prognosis, and treatment outcomes. This review will summarize the functional impact of key miR‐ SNP s and define a subset of miR‐ SNP s that may be clinically useful prognostic or predictive biomarkers.

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