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Exosomal miR-1304-3p promotes breast cancer progression in African Americans by activating cancer-associated adipocytes

Breast cancer displays disparities in mortality between African Americans and Caucasian Americans. However, the exact molecular mechanisms remain elusive. Here, we identify miR-1304-3p as the most upregulated microRNA in African American patients. Importantly, its expression significantly correlates...

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Autores principales: Zhao, Dan, Wu, Kerui, Sharma, Sambad, Xing, Fei, Wu, Shih-Ying, Tyagi, Abhishek, Deshpande, Ravindra, Singh, Ravi, Wabitsch, Martin, Mo, Yin-Yuan, Watabe, Kounosuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751138/
https://www.ncbi.nlm.nih.gov/pubmed/36517516
http://dx.doi.org/10.1038/s41467-022-35305-2
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author Zhao, Dan
Wu, Kerui
Sharma, Sambad
Xing, Fei
Wu, Shih-Ying
Tyagi, Abhishek
Deshpande, Ravindra
Singh, Ravi
Wabitsch, Martin
Mo, Yin-Yuan
Watabe, Kounosuke
author_facet Zhao, Dan
Wu, Kerui
Sharma, Sambad
Xing, Fei
Wu, Shih-Ying
Tyagi, Abhishek
Deshpande, Ravindra
Singh, Ravi
Wabitsch, Martin
Mo, Yin-Yuan
Watabe, Kounosuke
author_sort Zhao, Dan
collection PubMed
description Breast cancer displays disparities in mortality between African Americans and Caucasian Americans. However, the exact molecular mechanisms remain elusive. Here, we identify miR-1304-3p as the most upregulated microRNA in African American patients. Importantly, its expression significantly correlates with poor progression-free survival in African American patients. Ectopic expression of miR-1304 promotes tumor progression in vivo. Exosomal miR-1304-3p activates cancer-associated adipocytes that release lipids and enhance cancer cell growth. Moreover, we identify the anti-adipogenic gene GATA2 as the target of miR-1304-3p. Notably, a single nucleotide polymorphism (SNP) located in the miR-1304 stem-loop region shows a significant difference in frequencies of the G allele between African and Caucasian American groups, which promotes the maturation of miR-1304-3p. Therefore, our results reveal a mechanism of the disparity in breast cancer progression and suggest a potential utility of miR-1304-3p and the associated SNP as biomarkers for predicting the outcome of African American patients.
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spelling pubmed-97511382022-12-16 Exosomal miR-1304-3p promotes breast cancer progression in African Americans by activating cancer-associated adipocytes Zhao, Dan Wu, Kerui Sharma, Sambad Xing, Fei Wu, Shih-Ying Tyagi, Abhishek Deshpande, Ravindra Singh, Ravi Wabitsch, Martin Mo, Yin-Yuan Watabe, Kounosuke Nat Commun Article Breast cancer displays disparities in mortality between African Americans and Caucasian Americans. However, the exact molecular mechanisms remain elusive. Here, we identify miR-1304-3p as the most upregulated microRNA in African American patients. Importantly, its expression significantly correlates with poor progression-free survival in African American patients. Ectopic expression of miR-1304 promotes tumor progression in vivo. Exosomal miR-1304-3p activates cancer-associated adipocytes that release lipids and enhance cancer cell growth. Moreover, we identify the anti-adipogenic gene GATA2 as the target of miR-1304-3p. Notably, a single nucleotide polymorphism (SNP) located in the miR-1304 stem-loop region shows a significant difference in frequencies of the G allele between African and Caucasian American groups, which promotes the maturation of miR-1304-3p. Therefore, our results reveal a mechanism of the disparity in breast cancer progression and suggest a potential utility of miR-1304-3p and the associated SNP as biomarkers for predicting the outcome of African American patients. Nature Publishing Group UK 2022-12-14 /pmc/articles/PMC9751138/ /pubmed/36517516 http://dx.doi.org/10.1038/s41467-022-35305-2 Text en © The Author(s) 2022, corrected publication 2023 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhao, Dan
Wu, Kerui
Sharma, Sambad
Xing, Fei
Wu, Shih-Ying
Tyagi, Abhishek
Deshpande, Ravindra
Singh, Ravi
Wabitsch, Martin
Mo, Yin-Yuan
Watabe, Kounosuke
Exosomal miR-1304-3p promotes breast cancer progression in African Americans by activating cancer-associated adipocytes
title Exosomal miR-1304-3p promotes breast cancer progression in African Americans by activating cancer-associated adipocytes
title_full Exosomal miR-1304-3p promotes breast cancer progression in African Americans by activating cancer-associated adipocytes
title_fullStr Exosomal miR-1304-3p promotes breast cancer progression in African Americans by activating cancer-associated adipocytes
title_full_unstemmed Exosomal miR-1304-3p promotes breast cancer progression in African Americans by activating cancer-associated adipocytes
title_short Exosomal miR-1304-3p promotes breast cancer progression in African Americans by activating cancer-associated adipocytes
title_sort exosomal mir-1304-3p promotes breast cancer progression in african americans by activating cancer-associated adipocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751138/
https://www.ncbi.nlm.nih.gov/pubmed/36517516
http://dx.doi.org/10.1038/s41467-022-35305-2
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