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Association of Body Mass Index With Somatic Mutations in Breast Cancer

BACKGROUND: The relationship between body mass index (BMI) and the prognosis or treatment response in patients with breast cancer has been demonstrated in previous studies, but the somatic mutation profiles in breast cancer patients with different BMIs have not been explored. METHODS: In the present...

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Autores principales: Chen, Bo, Guo, Liping, Li, Kai, Xiao, Weikai, Li, Yingzi, Li, Cheukfai, Mok, Hsiaopei, Cao, Li, Lin, Jiali, Wei, Guangnan, Zhang, Guochun, Liao, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049504/
https://www.ncbi.nlm.nih.gov/pubmed/33868999
http://dx.doi.org/10.3389/fonc.2021.613933
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author Chen, Bo
Guo, Liping
Li, Kai
Xiao, Weikai
Li, Yingzi
Li, Cheukfai
Mok, Hsiaopei
Cao, Li
Lin, Jiali
Wei, Guangnan
Zhang, Guochun
Liao, Ning
author_facet Chen, Bo
Guo, Liping
Li, Kai
Xiao, Weikai
Li, Yingzi
Li, Cheukfai
Mok, Hsiaopei
Cao, Li
Lin, Jiali
Wei, Guangnan
Zhang, Guochun
Liao, Ning
author_sort Chen, Bo
collection PubMed
description BACKGROUND: The relationship between body mass index (BMI) and the prognosis or treatment response in patients with breast cancer has been demonstrated in previous studies, but the somatic mutation profiles in breast cancer patients with different BMIs have not been explored. METHODS: In the present study, the somatic mutation profiles in 421 female breast cancer patients who were stratified into three subgroups based on BMI (normal weight, overweight/obese, and underweight) were investigated. Capture-based targeted sequencing was performed using a panel comprising 520 cancer-related genes. RESULTS: A total of 3547 mutations were detected in 390 genes. In breast cancer patients with different BMI statuses, the tumors exhibited high mutation frequency and burden. TP53 was the most common gene in the three groups, followed by PIK3CA, ERBB2, and CDK12. Meanwhile, the mutation hotspots in TP53 and PIK3CA were the same in the three BMI groups. More JAK1 mutations were identified in underweight patients than those in normal patients. Except for JAK1, differentially mutated genes in postmenopausal patients were completely different from those in premenopausal patients. The distribution of mutation types was significantly different among BMI groups in the postmenopausal group. Underweight patients in the postmenopausal group harbored more TP53 mutations, more amplifications, and more mutations in genes involved in the WNT signaling pathway. CONCLUSIONS: Our next-generation sequencing (NGS)-based gene panel analysis revealed the gene expression profiles of breast cancer patients with different BMI statuses. Although genes with high mutation frequency and burden were found in different BMI groups, some subtle differences could not be ignored. JAK1 mutations might play a vital role in the progression of breast cancer in underweight patients, and this needs further analysis. Postmenopausal underweight patients with breast cancer have more aggressive characteristics, such as TP53 mutations, more amplifications, and more mutations in genes involved in the WNT signaling pathway. This study provides new evidence for understanding the characteristics of breast cancer patients with different BMIs.
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spelling pubmed-80495042021-04-16 Association of Body Mass Index With Somatic Mutations in Breast Cancer Chen, Bo Guo, Liping Li, Kai Xiao, Weikai Li, Yingzi Li, Cheukfai Mok, Hsiaopei Cao, Li Lin, Jiali Wei, Guangnan Zhang, Guochun Liao, Ning Front Oncol Oncology BACKGROUND: The relationship between body mass index (BMI) and the prognosis or treatment response in patients with breast cancer has been demonstrated in previous studies, but the somatic mutation profiles in breast cancer patients with different BMIs have not been explored. METHODS: In the present study, the somatic mutation profiles in 421 female breast cancer patients who were stratified into three subgroups based on BMI (normal weight, overweight/obese, and underweight) were investigated. Capture-based targeted sequencing was performed using a panel comprising 520 cancer-related genes. RESULTS: A total of 3547 mutations were detected in 390 genes. In breast cancer patients with different BMI statuses, the tumors exhibited high mutation frequency and burden. TP53 was the most common gene in the three groups, followed by PIK3CA, ERBB2, and CDK12. Meanwhile, the mutation hotspots in TP53 and PIK3CA were the same in the three BMI groups. More JAK1 mutations were identified in underweight patients than those in normal patients. Except for JAK1, differentially mutated genes in postmenopausal patients were completely different from those in premenopausal patients. The distribution of mutation types was significantly different among BMI groups in the postmenopausal group. Underweight patients in the postmenopausal group harbored more TP53 mutations, more amplifications, and more mutations in genes involved in the WNT signaling pathway. CONCLUSIONS: Our next-generation sequencing (NGS)-based gene panel analysis revealed the gene expression profiles of breast cancer patients with different BMI statuses. Although genes with high mutation frequency and burden were found in different BMI groups, some subtle differences could not be ignored. JAK1 mutations might play a vital role in the progression of breast cancer in underweight patients, and this needs further analysis. Postmenopausal underweight patients with breast cancer have more aggressive characteristics, such as TP53 mutations, more amplifications, and more mutations in genes involved in the WNT signaling pathway. This study provides new evidence for understanding the characteristics of breast cancer patients with different BMIs. Frontiers Media S.A. 2021-04-01 /pmc/articles/PMC8049504/ /pubmed/33868999 http://dx.doi.org/10.3389/fonc.2021.613933 Text en Copyright © 2021 Chen, Guo, Li, Xiao, Li, Li, Mok, Cao, Lin, Wei, Zhang and Liao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Chen, Bo
Guo, Liping
Li, Kai
Xiao, Weikai
Li, Yingzi
Li, Cheukfai
Mok, Hsiaopei
Cao, Li
Lin, Jiali
Wei, Guangnan
Zhang, Guochun
Liao, Ning
Association of Body Mass Index With Somatic Mutations in Breast Cancer
title Association of Body Mass Index With Somatic Mutations in Breast Cancer
title_full Association of Body Mass Index With Somatic Mutations in Breast Cancer
title_fullStr Association of Body Mass Index With Somatic Mutations in Breast Cancer
title_full_unstemmed Association of Body Mass Index With Somatic Mutations in Breast Cancer
title_short Association of Body Mass Index With Somatic Mutations in Breast Cancer
title_sort association of body mass index with somatic mutations in breast cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049504/
https://www.ncbi.nlm.nih.gov/pubmed/33868999
http://dx.doi.org/10.3389/fonc.2021.613933
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