Cargando…

PIK3CA somatic alterations in invasive breast cancers: different spectrum from Caucasians to Chinese detected by next generation sequencing

PURPOSE: Somatic alteration of phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) is a crucial therapeutic target in breast cancer (BC) and PI3Kα-specific inhibitor Alpelisib has been used in clinics. This study investigates the PIK3CA alterations in Chinese and Caucasia...

Descripción completa

Detalles Bibliográficos
Autores principales: Jia, Minghan, Liao, Ning, Chen, Bo, Zhang, Guochun, Wang, Yulei, Li, Xuerui, Cao, Li, Mok, Hsiaopei, Ren, Chongyang, Li, Kai, Li, Cheukfai, Wen, Lingzhu, Lin, Jiali, Wei, Guangnan, Balch, Charles M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065000/
https://www.ncbi.nlm.nih.gov/pubmed/33386585
http://dx.doi.org/10.1007/s12282-020-01199-5
_version_ 1783682249796878336
author Jia, Minghan
Liao, Ning
Chen, Bo
Zhang, Guochun
Wang, Yulei
Li, Xuerui
Cao, Li
Mok, Hsiaopei
Ren, Chongyang
Li, Kai
Li, Cheukfai
Wen, Lingzhu
Lin, Jiali
Wei, Guangnan
Balch, Charles M.
author_facet Jia, Minghan
Liao, Ning
Chen, Bo
Zhang, Guochun
Wang, Yulei
Li, Xuerui
Cao, Li
Mok, Hsiaopei
Ren, Chongyang
Li, Kai
Li, Cheukfai
Wen, Lingzhu
Lin, Jiali
Wei, Guangnan
Balch, Charles M.
author_sort Jia, Minghan
collection PubMed
description PURPOSE: Somatic alteration of phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) is a crucial therapeutic target in breast cancer (BC) and PI3Kα-specific inhibitor Alpelisib has been used in clinics. This study investigates the PIK3CA alterations in Chinese and Caucasians BC patients for the purpose of selecting anti-PI3K therapy. METHODS: The molecular profile of the PIK3CA gene was analyzed in 412 Chinese patients with untreated invasive BC using a 540 gene next-generation sequencing panel. The results were compared with data of the Caucasian BC patients in The Cancer Genome Atlas (TCGA-white). RESULTS: PIK3CA alterations were frequently found in BC of estrogen receptor (ER) positive (49.3%, p = 0.024), low ki67 proliferation index (58.3%, p = 0.007) and low pathological grade (grade I/II/III 80%, 53.4%, 35.9%, p < 0.001). Compared to TCGA-white, Chinese BC patients had a higher alteration frequency (45.6% vs. 34.7%, p < 0.001) with larger proportion of p.H1047R mutation among three common mutation sites (p.E545K, p.E542K and p.H1047R) (66.1% vs. 43.7%, p = 0.01). Across four molecular subtypes, ER + /human epidermal growth factor receptor 2 positive (HER2 +) tumors harbored the most PIK3CA alterations (51.6%), while ER-/HER2- harbored the least alteration (30.0%) but the most copy number amplification (19.05%). CONCLUSION: PIK3CA alterations prevail in Chinese BC patients and have different molecular features compared to that of Caucasians. The results provide precise annotations of PIK3CA genomic alterations of Chinese in the context of application of PIK3CA inhibitor.
format Online
Article
Text
id pubmed-8065000
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer Singapore
record_format MEDLINE/PubMed
spelling pubmed-80650002021-05-05 PIK3CA somatic alterations in invasive breast cancers: different spectrum from Caucasians to Chinese detected by next generation sequencing Jia, Minghan Liao, Ning Chen, Bo Zhang, Guochun Wang, Yulei Li, Xuerui Cao, Li Mok, Hsiaopei Ren, Chongyang Li, Kai Li, Cheukfai Wen, Lingzhu Lin, Jiali Wei, Guangnan Balch, Charles M. Breast Cancer Original Article PURPOSE: Somatic alteration of phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) is a crucial therapeutic target in breast cancer (BC) and PI3Kα-specific inhibitor Alpelisib has been used in clinics. This study investigates the PIK3CA alterations in Chinese and Caucasians BC patients for the purpose of selecting anti-PI3K therapy. METHODS: The molecular profile of the PIK3CA gene was analyzed in 412 Chinese patients with untreated invasive BC using a 540 gene next-generation sequencing panel. The results were compared with data of the Caucasian BC patients in The Cancer Genome Atlas (TCGA-white). RESULTS: PIK3CA alterations were frequently found in BC of estrogen receptor (ER) positive (49.3%, p = 0.024), low ki67 proliferation index (58.3%, p = 0.007) and low pathological grade (grade I/II/III 80%, 53.4%, 35.9%, p < 0.001). Compared to TCGA-white, Chinese BC patients had a higher alteration frequency (45.6% vs. 34.7%, p < 0.001) with larger proportion of p.H1047R mutation among three common mutation sites (p.E545K, p.E542K and p.H1047R) (66.1% vs. 43.7%, p = 0.01). Across four molecular subtypes, ER + /human epidermal growth factor receptor 2 positive (HER2 +) tumors harbored the most PIK3CA alterations (51.6%), while ER-/HER2- harbored the least alteration (30.0%) but the most copy number amplification (19.05%). CONCLUSION: PIK3CA alterations prevail in Chinese BC patients and have different molecular features compared to that of Caucasians. The results provide precise annotations of PIK3CA genomic alterations of Chinese in the context of application of PIK3CA inhibitor. Springer Singapore 2021-01-01 2021 /pmc/articles/PMC8065000/ /pubmed/33386585 http://dx.doi.org/10.1007/s12282-020-01199-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Jia, Minghan
Liao, Ning
Chen, Bo
Zhang, Guochun
Wang, Yulei
Li, Xuerui
Cao, Li
Mok, Hsiaopei
Ren, Chongyang
Li, Kai
Li, Cheukfai
Wen, Lingzhu
Lin, Jiali
Wei, Guangnan
Balch, Charles M.
PIK3CA somatic alterations in invasive breast cancers: different spectrum from Caucasians to Chinese detected by next generation sequencing
title PIK3CA somatic alterations in invasive breast cancers: different spectrum from Caucasians to Chinese detected by next generation sequencing
title_full PIK3CA somatic alterations in invasive breast cancers: different spectrum from Caucasians to Chinese detected by next generation sequencing
title_fullStr PIK3CA somatic alterations in invasive breast cancers: different spectrum from Caucasians to Chinese detected by next generation sequencing
title_full_unstemmed PIK3CA somatic alterations in invasive breast cancers: different spectrum from Caucasians to Chinese detected by next generation sequencing
title_short PIK3CA somatic alterations in invasive breast cancers: different spectrum from Caucasians to Chinese detected by next generation sequencing
title_sort pik3ca somatic alterations in invasive breast cancers: different spectrum from caucasians to chinese detected by next generation sequencing
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065000/
https://www.ncbi.nlm.nih.gov/pubmed/33386585
http://dx.doi.org/10.1007/s12282-020-01199-5
work_keys_str_mv AT jiaminghan pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT liaoning pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT chenbo pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT zhangguochun pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT wangyulei pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT lixuerui pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT caoli pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT mokhsiaopei pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT renchongyang pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT likai pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT licheukfai pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT wenlingzhu pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT linjiali pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT weiguangnan pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing
AT balchcharlesm pik3casomaticalterationsininvasivebreastcancersdifferentspectrumfromcaucasianstochinesedetectedbynextgenerationsequencing