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Differences in gene mutations according to gender among patients with colorectal cancer
BACKGROUND: The incidence, site distribution, and mortality rates of patients with colorectal cancer differ according to gender. We investigated gene mutations in colorectal patients and wanted to examine gender-specific differences. METHODS: A total of 1505 patients who underwent surgical intervent...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034318/ https://www.ncbi.nlm.nih.gov/pubmed/29976257 http://dx.doi.org/10.1186/s12957-018-1431-5 |
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author | Tsai, Yi-Jian Huang, Sheng-Chieh Lin, Hung-Hsin Lin, Chun-Chi Lan, Yuan-Tzu Wang, Huann-Sheng Yang, Shung-Haur Jiang, Jeng-Kai Chen, Wei-Shone Lin, Tzu-chen Lin, Jen-Kou Chang, Shih-Ching |
author_facet | Tsai, Yi-Jian Huang, Sheng-Chieh Lin, Hung-Hsin Lin, Chun-Chi Lan, Yuan-Tzu Wang, Huann-Sheng Yang, Shung-Haur Jiang, Jeng-Kai Chen, Wei-Shone Lin, Tzu-chen Lin, Jen-Kou Chang, Shih-Ching |
author_sort | Tsai, Yi-Jian |
collection | PubMed |
description | BACKGROUND: The incidence, site distribution, and mortality rates of patients with colorectal cancer differ according to gender. We investigated gene mutations in colorectal patients and wanted to examine gender-specific differences. METHODS: A total of 1505 patients who underwent surgical intervention for colorectal cancer were recruited from March 2000 to January 2010 at Taipei Veterans’ General Hospital and investigated for gene mutations in K-ras, N-ras, H-ras, BRAF, loss of 18q, APC, p53, SMAD4, TGF-β, PIK3CA, PTEN, FBXW7, AKT1, and MSI. RESULTS: There were significant differences between male and female patients in terms of tumor location (p < 0.0001) and pathological stage (p = 0.011). The female patients had significantly more gene mutations in BRAF (6.4 vs. 3.3%, OR 1.985, p = 0.006), TGF-β (4.7 vs. 2.5%, OR 1.887, p = 0.027), and revealed a MSI-high status (14.0 vs. 8.3%, OR 1.800, p = 0.001) than male patients. Male patients had significantly more gene mutations in N-ras (5.1 vs. 2.3%, OR 2.227, p = 0.012); however, the significance was maintained only for mutations in BRAF (OR 2.104, p = 0.038), MSI-high status (OR 2.003 p = 0.001), and N-ras (OR 3.000, p = 0.010) after the groups were divided by tumor site. CONCLUSION: Gene mutations in BRAF, MSI-high status, and N-ras differ according to gender among patients with colorectal cancer. |
format | Online Article Text |
id | pubmed-6034318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60343182018-07-09 Differences in gene mutations according to gender among patients with colorectal cancer Tsai, Yi-Jian Huang, Sheng-Chieh Lin, Hung-Hsin Lin, Chun-Chi Lan, Yuan-Tzu Wang, Huann-Sheng Yang, Shung-Haur Jiang, Jeng-Kai Chen, Wei-Shone Lin, Tzu-chen Lin, Jen-Kou Chang, Shih-Ching World J Surg Oncol Research BACKGROUND: The incidence, site distribution, and mortality rates of patients with colorectal cancer differ according to gender. We investigated gene mutations in colorectal patients and wanted to examine gender-specific differences. METHODS: A total of 1505 patients who underwent surgical intervention for colorectal cancer were recruited from March 2000 to January 2010 at Taipei Veterans’ General Hospital and investigated for gene mutations in K-ras, N-ras, H-ras, BRAF, loss of 18q, APC, p53, SMAD4, TGF-β, PIK3CA, PTEN, FBXW7, AKT1, and MSI. RESULTS: There were significant differences between male and female patients in terms of tumor location (p < 0.0001) and pathological stage (p = 0.011). The female patients had significantly more gene mutations in BRAF (6.4 vs. 3.3%, OR 1.985, p = 0.006), TGF-β (4.7 vs. 2.5%, OR 1.887, p = 0.027), and revealed a MSI-high status (14.0 vs. 8.3%, OR 1.800, p = 0.001) than male patients. Male patients had significantly more gene mutations in N-ras (5.1 vs. 2.3%, OR 2.227, p = 0.012); however, the significance was maintained only for mutations in BRAF (OR 2.104, p = 0.038), MSI-high status (OR 2.003 p = 0.001), and N-ras (OR 3.000, p = 0.010) after the groups were divided by tumor site. CONCLUSION: Gene mutations in BRAF, MSI-high status, and N-ras differ according to gender among patients with colorectal cancer. BioMed Central 2018-07-05 /pmc/articles/PMC6034318/ /pubmed/29976257 http://dx.doi.org/10.1186/s12957-018-1431-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Tsai, Yi-Jian Huang, Sheng-Chieh Lin, Hung-Hsin Lin, Chun-Chi Lan, Yuan-Tzu Wang, Huann-Sheng Yang, Shung-Haur Jiang, Jeng-Kai Chen, Wei-Shone Lin, Tzu-chen Lin, Jen-Kou Chang, Shih-Ching Differences in gene mutations according to gender among patients with colorectal cancer |
title | Differences in gene mutations according to gender among patients with colorectal cancer |
title_full | Differences in gene mutations according to gender among patients with colorectal cancer |
title_fullStr | Differences in gene mutations according to gender among patients with colorectal cancer |
title_full_unstemmed | Differences in gene mutations according to gender among patients with colorectal cancer |
title_short | Differences in gene mutations according to gender among patients with colorectal cancer |
title_sort | differences in gene mutations according to gender among patients with colorectal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034318/ https://www.ncbi.nlm.nih.gov/pubmed/29976257 http://dx.doi.org/10.1186/s12957-018-1431-5 |
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