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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
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.
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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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