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The molecular landscape of Asian breast cancers reveals clinically relevant population-specific differences

Molecular profiling of breast cancer has enabled the development of more robust molecular prognostic signatures and therapeutic options for breast cancer patients. However, non-Caucasian populations remain understudied. Here, we present the mutational, transcriptional, and copy number profiles of 56...

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Autores principales: Pan, Jia-Wern, Zabidi, Muhammad Mamduh Ahmad, Ng, Pei-Sze, Meng, Mei-Yee, Hasan, Siti Norhidayu, Sandey, Bethan, Sammut, Stephen-John, Yip, Cheng-Har, Rajadurai, Pathmanathan, Rueda, Oscar M., Caldas, Carlos, Chin, Suet-Feung, Teo, Soo-Hwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755902/
https://www.ncbi.nlm.nih.gov/pubmed/33353943
http://dx.doi.org/10.1038/s41467-020-20173-5
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author Pan, Jia-Wern
Zabidi, Muhammad Mamduh Ahmad
Ng, Pei-Sze
Meng, Mei-Yee
Hasan, Siti Norhidayu
Sandey, Bethan
Sammut, Stephen-John
Yip, Cheng-Har
Rajadurai, Pathmanathan
Rueda, Oscar M.
Caldas, Carlos
Chin, Suet-Feung
Teo, Soo-Hwang
author_facet Pan, Jia-Wern
Zabidi, Muhammad Mamduh Ahmad
Ng, Pei-Sze
Meng, Mei-Yee
Hasan, Siti Norhidayu
Sandey, Bethan
Sammut, Stephen-John
Yip, Cheng-Har
Rajadurai, Pathmanathan
Rueda, Oscar M.
Caldas, Carlos
Chin, Suet-Feung
Teo, Soo-Hwang
author_sort Pan, Jia-Wern
collection PubMed
description Molecular profiling of breast cancer has enabled the development of more robust molecular prognostic signatures and therapeutic options for breast cancer patients. However, non-Caucasian populations remain understudied. Here, we present the mutational, transcriptional, and copy number profiles of 560 Malaysian breast tumours and a comparative analysis of breast cancers arising in Asian and Caucasian women. Compared to breast tumours in Caucasian women, we show an increased prevalence of HER2-enriched molecular subtypes and higher prevalence of TP53 somatic mutations in ER+ Asian breast tumours. We also observe elevated immune scores in Asian breast tumours, suggesting potential clinical response to immune checkpoint inhibitors. Whilst HER2-subtype and enriched immune score are associated with improved survival, presence of TP53 somatic mutations is associated with poorer survival in ER+ tumours. Taken together, these population differences unveil opportunities to improve the understanding of this disease and lay the foundation for precision medicine in different populations.
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spelling pubmed-77559022021-01-11 The molecular landscape of Asian breast cancers reveals clinically relevant population-specific differences Pan, Jia-Wern Zabidi, Muhammad Mamduh Ahmad Ng, Pei-Sze Meng, Mei-Yee Hasan, Siti Norhidayu Sandey, Bethan Sammut, Stephen-John Yip, Cheng-Har Rajadurai, Pathmanathan Rueda, Oscar M. Caldas, Carlos Chin, Suet-Feung Teo, Soo-Hwang Nat Commun Article Molecular profiling of breast cancer has enabled the development of more robust molecular prognostic signatures and therapeutic options for breast cancer patients. However, non-Caucasian populations remain understudied. Here, we present the mutational, transcriptional, and copy number profiles of 560 Malaysian breast tumours and a comparative analysis of breast cancers arising in Asian and Caucasian women. Compared to breast tumours in Caucasian women, we show an increased prevalence of HER2-enriched molecular subtypes and higher prevalence of TP53 somatic mutations in ER+ Asian breast tumours. We also observe elevated immune scores in Asian breast tumours, suggesting potential clinical response to immune checkpoint inhibitors. Whilst HER2-subtype and enriched immune score are associated with improved survival, presence of TP53 somatic mutations is associated with poorer survival in ER+ tumours. Taken together, these population differences unveil opportunities to improve the understanding of this disease and lay the foundation for precision medicine in different populations. Nature Publishing Group UK 2020-12-22 /pmc/articles/PMC7755902/ /pubmed/33353943 http://dx.doi.org/10.1038/s41467-020-20173-5 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pan, Jia-Wern
Zabidi, Muhammad Mamduh Ahmad
Ng, Pei-Sze
Meng, Mei-Yee
Hasan, Siti Norhidayu
Sandey, Bethan
Sammut, Stephen-John
Yip, Cheng-Har
Rajadurai, Pathmanathan
Rueda, Oscar M.
Caldas, Carlos
Chin, Suet-Feung
Teo, Soo-Hwang
The molecular landscape of Asian breast cancers reveals clinically relevant population-specific differences
title The molecular landscape of Asian breast cancers reveals clinically relevant population-specific differences
title_full The molecular landscape of Asian breast cancers reveals clinically relevant population-specific differences
title_fullStr The molecular landscape of Asian breast cancers reveals clinically relevant population-specific differences
title_full_unstemmed The molecular landscape of Asian breast cancers reveals clinically relevant population-specific differences
title_short The molecular landscape of Asian breast cancers reveals clinically relevant population-specific differences
title_sort molecular landscape of asian breast cancers reveals clinically relevant population-specific differences
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755902/
https://www.ncbi.nlm.nih.gov/pubmed/33353943
http://dx.doi.org/10.1038/s41467-020-20173-5
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