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Single Nucleotide Polymorphisms in MicroRNA Binding Sites: Implications in Colorectal Cancer
Cancer is a complex genetic disorder, characterised by uncontrolled cell proliferation and caused by altered expression of oncogenes and tumour suppressor genes. When cell proliferation pertains to colon, it is called colorectal cancer. Most of colorectal cancer causing genes are potential targets f...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310495/ https://www.ncbi.nlm.nih.gov/pubmed/25654126 http://dx.doi.org/10.1155/2014/547154 |
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author | Bhaumik, Panchalee Gopalakrishnan, Chandrasekhar Kamaraj, Balu Purohit, Rituraj |
author_facet | Bhaumik, Panchalee Gopalakrishnan, Chandrasekhar Kamaraj, Balu Purohit, Rituraj |
author_sort | Bhaumik, Panchalee |
collection | PubMed |
description | Cancer is a complex genetic disorder, characterised by uncontrolled cell proliferation and caused by altered expression of oncogenes and tumour suppressor genes. When cell proliferation pertains to colon, it is called colorectal cancer. Most of colorectal cancer causing genes are potential targets for the miRNA (microRNA) that bind to 3′UTR (untranslated regions) of mRNA and inhibit translation. Mutations occurring in miRNA binding regions can alter the miRNA, mRNA combination, and can alter gene expression drastically. We hypothesized that 3′UTR mutation in miRNA binding site could alter the miRNA, mRNA interaction, thereby altering gene expression. Altered gene expression activity could promote tumorigenesis in colon. Therefore, we formulated a systematic in silico procedure that integrates data from various databases, followed rigorous selection criteria, and identified mutations that might alter the expression levels of cancer causing genes. Further we performed expression analysis to shed light on the potential tissues that might be affected by mutation, enrichment analysis to find the metabolic functions of the gene, and network analysis to highlight the important interactions of cancer causing genes with other genes to provide insight that complex network will be disturbed upon mutation. We provide in silico evidence for the effect of these mutations in colorectal cancer. |
format | Online Article Text |
id | pubmed-4310495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-43104952015-02-04 Single Nucleotide Polymorphisms in MicroRNA Binding Sites: Implications in Colorectal Cancer Bhaumik, Panchalee Gopalakrishnan, Chandrasekhar Kamaraj, Balu Purohit, Rituraj ScientificWorldJournal Research Article Cancer is a complex genetic disorder, characterised by uncontrolled cell proliferation and caused by altered expression of oncogenes and tumour suppressor genes. When cell proliferation pertains to colon, it is called colorectal cancer. Most of colorectal cancer causing genes are potential targets for the miRNA (microRNA) that bind to 3′UTR (untranslated regions) of mRNA and inhibit translation. Mutations occurring in miRNA binding regions can alter the miRNA, mRNA combination, and can alter gene expression drastically. We hypothesized that 3′UTR mutation in miRNA binding site could alter the miRNA, mRNA interaction, thereby altering gene expression. Altered gene expression activity could promote tumorigenesis in colon. Therefore, we formulated a systematic in silico procedure that integrates data from various databases, followed rigorous selection criteria, and identified mutations that might alter the expression levels of cancer causing genes. Further we performed expression analysis to shed light on the potential tissues that might be affected by mutation, enrichment analysis to find the metabolic functions of the gene, and network analysis to highlight the important interactions of cancer causing genes with other genes to provide insight that complex network will be disturbed upon mutation. We provide in silico evidence for the effect of these mutations in colorectal cancer. Hindawi Publishing Corporation 2014 2014-12-24 /pmc/articles/PMC4310495/ /pubmed/25654126 http://dx.doi.org/10.1155/2014/547154 Text en Copyright © 2014 Panchalee Bhaumik et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bhaumik, Panchalee Gopalakrishnan, Chandrasekhar Kamaraj, Balu Purohit, Rituraj Single Nucleotide Polymorphisms in MicroRNA Binding Sites: Implications in Colorectal Cancer |
title | Single Nucleotide Polymorphisms in MicroRNA Binding Sites: Implications in Colorectal Cancer |
title_full | Single Nucleotide Polymorphisms in MicroRNA Binding Sites: Implications in Colorectal Cancer |
title_fullStr | Single Nucleotide Polymorphisms in MicroRNA Binding Sites: Implications in Colorectal Cancer |
title_full_unstemmed | Single Nucleotide Polymorphisms in MicroRNA Binding Sites: Implications in Colorectal Cancer |
title_short | Single Nucleotide Polymorphisms in MicroRNA Binding Sites: Implications in Colorectal Cancer |
title_sort | single nucleotide polymorphisms in microrna binding sites: implications in colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310495/ https://www.ncbi.nlm.nih.gov/pubmed/25654126 http://dx.doi.org/10.1155/2014/547154 |
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