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HER2 and BRAF mutation in colorectal cancer patients: a retrospective study in Eastern China

OBJECTIVE: To investigate the frequency and prognostic role of the human epidermal growth factor receptor 2 gene (HER2) and BRAF V600E gene mutation in Chinese patients with colorectal cancer (CRC). METHODS: Clinicopathological and survival information from 480 patients with stage I–III CRC were rev...

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Autores principales: Zhang, Xiangyan, Wu, Jie, Wang, Lili, Zhao, Han, Li, Hong, Duan, Yuhe, Li, Yujun, Xu, Ping, Ran, Wenwen, Xing, Xiaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023828/
https://www.ncbi.nlm.nih.gov/pubmed/32095377
http://dx.doi.org/10.7717/peerj.8602
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author Zhang, Xiangyan
Wu, Jie
Wang, Lili
Zhao, Han
Li, Hong
Duan, Yuhe
Li, Yujun
Xu, Ping
Ran, Wenwen
Xing, Xiaoming
author_facet Zhang, Xiangyan
Wu, Jie
Wang, Lili
Zhao, Han
Li, Hong
Duan, Yuhe
Li, Yujun
Xu, Ping
Ran, Wenwen
Xing, Xiaoming
author_sort Zhang, Xiangyan
collection PubMed
description OBJECTIVE: To investigate the frequency and prognostic role of the human epidermal growth factor receptor 2 gene (HER2) and BRAF V600E gene mutation in Chinese patients with colorectal cancer (CRC). METHODS: Clinicopathological and survival information from 480 patients with stage I–III CRC were reviewed and recorded. HER2 amplification was analyzed by immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH), BRAF V600E mutation was tested by IHC and Sanger sequencing. The relationship between HER2 and BRAF V600E mutation status and clinicopathological characteristics and outcomes were determined. RESULTS: The amplification of HER2 and BRAF V600E mutation were identified in 27 of 480 (5.63%) and 19 of 480 (3.96%) CRC patients, respectively. HER2 amplification significantly correlated with greater bowel wall invasion (P = 0.041) and more advanced TNM stage (I vs. II vs. III; 0 vs 5.78% vs. 7.41%, P = 0.013). Patients suffering from tumors with poor differentiation had a higher incidence rate of BRAF V600E mutation than those with moderate/well differentiation (7.77% vs 2.92%, P = 0.04). HER2 amplification was an independent prognostic factor for worse disease-free survival (DFS) (HR = 2.53, 95% CI: 1.21–5.30, P = 0.014). CONCLUSION: The prevalence of HER2 amplification and BRAF V600E mutation in stage I–III CRC patients in Chinese was 6% and 4%, respectively, and HER2 amplification appeared to be associated with a worse DFS. More comprehensive molecular classification and survival analysis are needed to validate our findings.
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spelling pubmed-70238282020-02-24 HER2 and BRAF mutation in colorectal cancer patients: a retrospective study in Eastern China Zhang, Xiangyan Wu, Jie Wang, Lili Zhao, Han Li, Hong Duan, Yuhe Li, Yujun Xu, Ping Ran, Wenwen Xing, Xiaoming PeerJ Gastroenterology and Hepatology OBJECTIVE: To investigate the frequency and prognostic role of the human epidermal growth factor receptor 2 gene (HER2) and BRAF V600E gene mutation in Chinese patients with colorectal cancer (CRC). METHODS: Clinicopathological and survival information from 480 patients with stage I–III CRC were reviewed and recorded. HER2 amplification was analyzed by immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH), BRAF V600E mutation was tested by IHC and Sanger sequencing. The relationship between HER2 and BRAF V600E mutation status and clinicopathological characteristics and outcomes were determined. RESULTS: The amplification of HER2 and BRAF V600E mutation were identified in 27 of 480 (5.63%) and 19 of 480 (3.96%) CRC patients, respectively. HER2 amplification significantly correlated with greater bowel wall invasion (P = 0.041) and more advanced TNM stage (I vs. II vs. III; 0 vs 5.78% vs. 7.41%, P = 0.013). Patients suffering from tumors with poor differentiation had a higher incidence rate of BRAF V600E mutation than those with moderate/well differentiation (7.77% vs 2.92%, P = 0.04). HER2 amplification was an independent prognostic factor for worse disease-free survival (DFS) (HR = 2.53, 95% CI: 1.21–5.30, P = 0.014). CONCLUSION: The prevalence of HER2 amplification and BRAF V600E mutation in stage I–III CRC patients in Chinese was 6% and 4%, respectively, and HER2 amplification appeared to be associated with a worse DFS. More comprehensive molecular classification and survival analysis are needed to validate our findings. PeerJ Inc. 2020-02-12 /pmc/articles/PMC7023828/ /pubmed/32095377 http://dx.doi.org/10.7717/peerj.8602 Text en © 2020 Zhang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Gastroenterology and Hepatology
Zhang, Xiangyan
Wu, Jie
Wang, Lili
Zhao, Han
Li, Hong
Duan, Yuhe
Li, Yujun
Xu, Ping
Ran, Wenwen
Xing, Xiaoming
HER2 and BRAF mutation in colorectal cancer patients: a retrospective study in Eastern China
title HER2 and BRAF mutation in colorectal cancer patients: a retrospective study in Eastern China
title_full HER2 and BRAF mutation in colorectal cancer patients: a retrospective study in Eastern China
title_fullStr HER2 and BRAF mutation in colorectal cancer patients: a retrospective study in Eastern China
title_full_unstemmed HER2 and BRAF mutation in colorectal cancer patients: a retrospective study in Eastern China
title_short HER2 and BRAF mutation in colorectal cancer patients: a retrospective study in Eastern China
title_sort her2 and braf mutation in colorectal cancer patients: a retrospective study in eastern china
topic Gastroenterology and Hepatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023828/
https://www.ncbi.nlm.nih.gov/pubmed/32095377
http://dx.doi.org/10.7717/peerj.8602
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