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Chemokine receptors differentially expressed by race category and molecular subtype in the breast cancer TCGA cohort

Racial disparities in mortality due to metastasis remain significant among breast cancer patients. Chemokine receptors contribute to breast tumors and metastatic outcome. We explored for significant differences in chemokine receptor expression in breast tumors from Black, Asian, and White patients i...

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Autores principales: Vazquez, Elissa D., Fang, Xiangyi, Levesque, Lauren A., Huynh, Mike, Venegas, Citlali, Lu, Nhien, Salazar, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234040/
https://www.ncbi.nlm.nih.gov/pubmed/35754051
http://dx.doi.org/10.1038/s41598-022-14734-5
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author Vazquez, Elissa D.
Fang, Xiangyi
Levesque, Lauren A.
Huynh, Mike
Venegas, Citlali
Lu, Nhien
Salazar, Nicole
author_facet Vazquez, Elissa D.
Fang, Xiangyi
Levesque, Lauren A.
Huynh, Mike
Venegas, Citlali
Lu, Nhien
Salazar, Nicole
author_sort Vazquez, Elissa D.
collection PubMed
description Racial disparities in mortality due to metastasis remain significant among breast cancer patients. Chemokine receptors contribute to breast tumors and metastatic outcome. We explored for significant differences in chemokine receptor expression in breast tumors from Black, Asian, and White patients in The Cancer Genome Atlas. We show that despite sharing the same molecular subtype, expression of the chemokine receptors ACKR1, CCR3, CCR6, CCRL1, CCRL2, CXCR1, CXCR2, CXCR4, CXCR6, and CXC3CR1 was significantly different depending on racial group. For patients with triple negative breast cancer, CCR3 was higher in Black versus White and CCRL2 was higher in Asian versus White. In luminal A tumors, ACKR1 was lower in Asian versus White, CCR3 was higher in Black versus White, and CCR6 and CXC3CR1 were lower in Black versus White. In luminal B tumors, CCRL2 was lower in Black versus White, CXCR1 and CXC3CR1 were lower in Asian versus White, and CXCR2 was lower in Black and Asian versus White. In HER2 enriched tumors, CCR3 was higher in Black versus White and CXCR4 lower in Asian versus White. CCR3, CCR6, and CXCR6 associated with worse patient survival. These findings can inform improved treatment strategies to decrease racial disparities in breast cancer burden.
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spelling pubmed-92340402022-06-28 Chemokine receptors differentially expressed by race category and molecular subtype in the breast cancer TCGA cohort Vazquez, Elissa D. Fang, Xiangyi Levesque, Lauren A. Huynh, Mike Venegas, Citlali Lu, Nhien Salazar, Nicole Sci Rep Article Racial disparities in mortality due to metastasis remain significant among breast cancer patients. Chemokine receptors contribute to breast tumors and metastatic outcome. We explored for significant differences in chemokine receptor expression in breast tumors from Black, Asian, and White patients in The Cancer Genome Atlas. We show that despite sharing the same molecular subtype, expression of the chemokine receptors ACKR1, CCR3, CCR6, CCRL1, CCRL2, CXCR1, CXCR2, CXCR4, CXCR6, and CXC3CR1 was significantly different depending on racial group. For patients with triple negative breast cancer, CCR3 was higher in Black versus White and CCRL2 was higher in Asian versus White. In luminal A tumors, ACKR1 was lower in Asian versus White, CCR3 was higher in Black versus White, and CCR6 and CXC3CR1 were lower in Black versus White. In luminal B tumors, CCRL2 was lower in Black versus White, CXCR1 and CXC3CR1 were lower in Asian versus White, and CXCR2 was lower in Black and Asian versus White. In HER2 enriched tumors, CCR3 was higher in Black versus White and CXCR4 lower in Asian versus White. CCR3, CCR6, and CXCR6 associated with worse patient survival. These findings can inform improved treatment strategies to decrease racial disparities in breast cancer burden. Nature Publishing Group UK 2022-06-26 /pmc/articles/PMC9234040/ /pubmed/35754051 http://dx.doi.org/10.1038/s41598-022-14734-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 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 Article
Vazquez, Elissa D.
Fang, Xiangyi
Levesque, Lauren A.
Huynh, Mike
Venegas, Citlali
Lu, Nhien
Salazar, Nicole
Chemokine receptors differentially expressed by race category and molecular subtype in the breast cancer TCGA cohort
title Chemokine receptors differentially expressed by race category and molecular subtype in the breast cancer TCGA cohort
title_full Chemokine receptors differentially expressed by race category and molecular subtype in the breast cancer TCGA cohort
title_fullStr Chemokine receptors differentially expressed by race category and molecular subtype in the breast cancer TCGA cohort
title_full_unstemmed Chemokine receptors differentially expressed by race category and molecular subtype in the breast cancer TCGA cohort
title_short Chemokine receptors differentially expressed by race category and molecular subtype in the breast cancer TCGA cohort
title_sort chemokine receptors differentially expressed by race category and molecular subtype in the breast cancer tcga cohort
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234040/
https://www.ncbi.nlm.nih.gov/pubmed/35754051
http://dx.doi.org/10.1038/s41598-022-14734-5
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