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Role of APC and DNA mismatch repair genes in the development of colorectal cancers

Colorectal cancer is the third most common cause of cancer-related death in both men and women in the western hemisphere. According to the American Cancer Society, an estimated 105,500 new cases of colon cancer with 57,100 deaths will occur in the U.S. in 2003, accounting for about 10% of cancer dea...

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Detalles Bibliográficos
Autores principales: Narayan, Satya, Roy, Deodutta
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC317355/
https://www.ncbi.nlm.nih.gov/pubmed/14672538
http://dx.doi.org/10.1186/1476-4598-2-41
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author Narayan, Satya
Roy, Deodutta
author_facet Narayan, Satya
Roy, Deodutta
author_sort Narayan, Satya
collection PubMed
description Colorectal cancer is the third most common cause of cancer-related death in both men and women in the western hemisphere. According to the American Cancer Society, an estimated 105,500 new cases of colon cancer with 57,100 deaths will occur in the U.S. in 2003, accounting for about 10% of cancer deaths. Among the colon cancer patients, hereditary risk contributes approximately 20%. The main inherited colorectal cancers are the familial adenomatous polyposis (FAP) and the hereditary nonpolyposis colorectal cancers (HNPCC). The FAP and HNPCC are caused due to mutations in the adenomatous polyposis coli (APC) and DNA mismatch repair (MMR) genes. The focus of this review is to summarize the functions of APC and MMR gene products in the development of colorectal cancers.
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spelling pubmed-3173552004-01-23 Role of APC and DNA mismatch repair genes in the development of colorectal cancers Narayan, Satya Roy, Deodutta Mol Cancer Review Colorectal cancer is the third most common cause of cancer-related death in both men and women in the western hemisphere. According to the American Cancer Society, an estimated 105,500 new cases of colon cancer with 57,100 deaths will occur in the U.S. in 2003, accounting for about 10% of cancer deaths. Among the colon cancer patients, hereditary risk contributes approximately 20%. The main inherited colorectal cancers are the familial adenomatous polyposis (FAP) and the hereditary nonpolyposis colorectal cancers (HNPCC). The FAP and HNPCC are caused due to mutations in the adenomatous polyposis coli (APC) and DNA mismatch repair (MMR) genes. The focus of this review is to summarize the functions of APC and MMR gene products in the development of colorectal cancers. BioMed Central 2003-12-12 /pmc/articles/PMC317355/ /pubmed/14672538 http://dx.doi.org/10.1186/1476-4598-2-41 Text en Copyright © 2003 Narayan and Roy; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Review
Narayan, Satya
Roy, Deodutta
Role of APC and DNA mismatch repair genes in the development of colorectal cancers
title Role of APC and DNA mismatch repair genes in the development of colorectal cancers
title_full Role of APC and DNA mismatch repair genes in the development of colorectal cancers
title_fullStr Role of APC and DNA mismatch repair genes in the development of colorectal cancers
title_full_unstemmed Role of APC and DNA mismatch repair genes in the development of colorectal cancers
title_short Role of APC and DNA mismatch repair genes in the development of colorectal cancers
title_sort role of apc and dna mismatch repair genes in the development of colorectal cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC317355/
https://www.ncbi.nlm.nih.gov/pubmed/14672538
http://dx.doi.org/10.1186/1476-4598-2-41
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