Cargando…

Molecular spectrum of KRAS, NRAS, BRAF and PIK3CA mutations in Chinese colorectal cancer patients: analysis of 1,110 cases

Mutations in genes such as KRAS, NRAS, BRAF and PIK3CA have become an important part of colorectal carcinoma evaluation. The aim of this study was to screen for mutations in these genes in Chinese patients with colorectal cancer (CRC) and to explore their correlations with certain clinicopathologica...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Jing, Zheng, Jianming, Yang, Yinghong, Lu, Junliang, Gao, Jie, Lu, Tao, Sun, Jian, Jiang, Hui, Zhu, Yan, Zheng, Yuhui, Liang, Zhiyong, Liu, Tonghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687048/
https://www.ncbi.nlm.nih.gov/pubmed/26691448
http://dx.doi.org/10.1038/srep18678
_version_ 1782406550874226688
author Zhang, Jing
Zheng, Jianming
Yang, Yinghong
Lu, Junliang
Gao, Jie
Lu, Tao
Sun, Jian
Jiang, Hui
Zhu, Yan
Zheng, Yuhui
Liang, Zhiyong
Liu, Tonghua
author_facet Zhang, Jing
Zheng, Jianming
Yang, Yinghong
Lu, Junliang
Gao, Jie
Lu, Tao
Sun, Jian
Jiang, Hui
Zhu, Yan
Zheng, Yuhui
Liang, Zhiyong
Liu, Tonghua
author_sort Zhang, Jing
collection PubMed
description Mutations in genes such as KRAS, NRAS, BRAF and PIK3CA have become an important part of colorectal carcinoma evaluation. The aim of this study was to screen for mutations in these genes in Chinese patients with colorectal cancer (CRC) and to explore their correlations with certain clinicopathological parameters. We tested mutations in the KRAS (exons 2, 3 and 4), NRAS (exons 2, 3 and 4), PIK3CA (exon 20) and BRAF (exon 15) genes using reverse transcriptase-polymerase chain reaction (RT-PCR) and Sanger sequencing in a large cohort of 1,110 Chinese CRC patients who underwent surgical resection at one of three major teaching hospitals located in different regions of China. The prevalence rates of KRAS, NRAS, BRAF and PIK3CA mutations were 45.4%, 3.9%, 3.1% and 3.5%, respectively. Mutant KRAS was associated with the mucinous subtype and greater differentiation, while mutant BRAF was associated with right-sided tumors and poorer differentiation. Our results revealed differences in the genetic profiles of KRAS, NRAS, PIK3CA and BRAF at mutation hotspots between Chinese CRC patients and those of Western countries, while some of these gene features were shared among patients from other Asian countries.
format Online
Article
Text
id pubmed-4687048
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-46870482015-12-31 Molecular spectrum of KRAS, NRAS, BRAF and PIK3CA mutations in Chinese colorectal cancer patients: analysis of 1,110 cases Zhang, Jing Zheng, Jianming Yang, Yinghong Lu, Junliang Gao, Jie Lu, Tao Sun, Jian Jiang, Hui Zhu, Yan Zheng, Yuhui Liang, Zhiyong Liu, Tonghua Sci Rep Article Mutations in genes such as KRAS, NRAS, BRAF and PIK3CA have become an important part of colorectal carcinoma evaluation. The aim of this study was to screen for mutations in these genes in Chinese patients with colorectal cancer (CRC) and to explore their correlations with certain clinicopathological parameters. We tested mutations in the KRAS (exons 2, 3 and 4), NRAS (exons 2, 3 and 4), PIK3CA (exon 20) and BRAF (exon 15) genes using reverse transcriptase-polymerase chain reaction (RT-PCR) and Sanger sequencing in a large cohort of 1,110 Chinese CRC patients who underwent surgical resection at one of three major teaching hospitals located in different regions of China. The prevalence rates of KRAS, NRAS, BRAF and PIK3CA mutations were 45.4%, 3.9%, 3.1% and 3.5%, respectively. Mutant KRAS was associated with the mucinous subtype and greater differentiation, while mutant BRAF was associated with right-sided tumors and poorer differentiation. Our results revealed differences in the genetic profiles of KRAS, NRAS, PIK3CA and BRAF at mutation hotspots between Chinese CRC patients and those of Western countries, while some of these gene features were shared among patients from other Asian countries. Nature Publishing Group 2015-12-22 /pmc/articles/PMC4687048/ /pubmed/26691448 http://dx.doi.org/10.1038/srep18678 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhang, Jing
Zheng, Jianming
Yang, Yinghong
Lu, Junliang
Gao, Jie
Lu, Tao
Sun, Jian
Jiang, Hui
Zhu, Yan
Zheng, Yuhui
Liang, Zhiyong
Liu, Tonghua
Molecular spectrum of KRAS, NRAS, BRAF and PIK3CA mutations in Chinese colorectal cancer patients: analysis of 1,110 cases
title Molecular spectrum of KRAS, NRAS, BRAF and PIK3CA mutations in Chinese colorectal cancer patients: analysis of 1,110 cases
title_full Molecular spectrum of KRAS, NRAS, BRAF and PIK3CA mutations in Chinese colorectal cancer patients: analysis of 1,110 cases
title_fullStr Molecular spectrum of KRAS, NRAS, BRAF and PIK3CA mutations in Chinese colorectal cancer patients: analysis of 1,110 cases
title_full_unstemmed Molecular spectrum of KRAS, NRAS, BRAF and PIK3CA mutations in Chinese colorectal cancer patients: analysis of 1,110 cases
title_short Molecular spectrum of KRAS, NRAS, BRAF and PIK3CA mutations in Chinese colorectal cancer patients: analysis of 1,110 cases
title_sort molecular spectrum of kras, nras, braf and pik3ca mutations in chinese colorectal cancer patients: analysis of 1,110 cases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687048/
https://www.ncbi.nlm.nih.gov/pubmed/26691448
http://dx.doi.org/10.1038/srep18678
work_keys_str_mv AT zhangjing molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT zhengjianming molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT yangyinghong molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT lujunliang molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT gaojie molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT lutao molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT sunjian molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT jianghui molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT zhuyan molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT zhengyuhui molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT liangzhiyong molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases
AT liutonghua molecularspectrumofkrasnrasbrafandpik3camutationsinchinesecolorectalcancerpatientsanalysisof1110cases