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Functional microRNA binding site variants

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 con...

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Detalles Bibliográficos
Autores principales: Yuan, Ye, Weidhaas, Joanne B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322190/
https://www.ncbi.nlm.nih.gov/pubmed/30536617
http://dx.doi.org/10.1002/1878-0261.12421
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author Yuan, Ye
Weidhaas, Joanne B.
author_facet Yuan, Ye
Weidhaas, Joanne B.
author_sort Yuan, Ye
collection PubMed
description 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 microRNA binding sites can disrupt the regulation of hallmark biological pathways implicated in tumorigenesis and tumor progression. Many of these microRNA‐associated polymorphisms (miR‐SNPs) 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‐SNPs and define a subset of miR‐SNPs that may be clinically useful prognostic or predictive biomarkers.
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spelling pubmed-63221902019-01-10 Functional microRNA binding site variants Yuan, Ye Weidhaas, Joanne B. Mol Oncol Review Articles 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 microRNA binding sites can disrupt the regulation of hallmark biological pathways implicated in tumorigenesis and tumor progression. Many of these microRNA‐associated polymorphisms (miR‐SNPs) 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‐SNPs and define a subset of miR‐SNPs that may be clinically useful prognostic or predictive biomarkers. John Wiley and Sons Inc. 2018-12-26 2019-01 /pmc/articles/PMC6322190/ /pubmed/30536617 http://dx.doi.org/10.1002/1878-0261.12421 Text en © 2018 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Articles
Yuan, Ye
Weidhaas, Joanne B.
Functional microRNA binding site variants
title Functional microRNA binding site variants
title_full Functional microRNA binding site variants
title_fullStr Functional microRNA binding site variants
title_full_unstemmed Functional microRNA binding site variants
title_short Functional microRNA binding site variants
title_sort functional microrna binding site variants
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322190/
https://www.ncbi.nlm.nih.gov/pubmed/30536617
http://dx.doi.org/10.1002/1878-0261.12421
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