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Interaction between CD36 and FABP4 modulates adipocyte-induced fatty acid import and metabolism in breast cancer

Adipocytes influence breast cancer behaviour via fatty acid release into the tumour microenvironment. Co-culturing human adipocytes and breast cancer cells increased CD36 expression, with fatty acid import into breast cancer cells. Genetic ablation of CD36 attenuates adipocyte-induced epithelial-mes...

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Autores principales: Gyamfi, Jones, Yeo, Joo Hye, Kwon, Doru, Min, Byung Soh, Cha, Yoon Jin, Koo, Ja Seung, Jeong, Joon, Lee, Jinu, Choi, Junjeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463699/
https://www.ncbi.nlm.nih.gov/pubmed/34561446
http://dx.doi.org/10.1038/s41523-021-00324-7
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author Gyamfi, Jones
Yeo, Joo Hye
Kwon, Doru
Min, Byung Soh
Cha, Yoon Jin
Koo, Ja Seung
Jeong, Joon
Lee, Jinu
Choi, Junjeong
author_facet Gyamfi, Jones
Yeo, Joo Hye
Kwon, Doru
Min, Byung Soh
Cha, Yoon Jin
Koo, Ja Seung
Jeong, Joon
Lee, Jinu
Choi, Junjeong
author_sort Gyamfi, Jones
collection PubMed
description Adipocytes influence breast cancer behaviour via fatty acid release into the tumour microenvironment. Co-culturing human adipocytes and breast cancer cells increased CD36 expression, with fatty acid import into breast cancer cells. Genetic ablation of CD36 attenuates adipocyte-induced epithelial-mesenchymal transition (EMT) and stemness. We show a feedforward loop between CD36 and STAT3; where CD36 activates STAT3 signalling and STAT3 binds to the CD36 promoter, regulating its expression. CD36 expression results in metabolic reprogramming, with a shift towards fatty acid oxidation. CD36 inhibition induces de novo lipogenesis in breast cancer cells. Increased CD36 expression occurs with increased FABP4 expression. We showed that CD36 directly interacts with FABP4 to regulate fatty acid import, transport, and metabolism. CD36 and FABP4 inhibition induces apoptosis in tumour cells. These results indicate that CD36 mediates fatty acid import from adipocytes into cancer cells and activates signalling pathways that drive tumour progression. Targeting CD36 may have a potential for therapy, which will target the tumour microenvironment.
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spelling pubmed-84636992021-10-08 Interaction between CD36 and FABP4 modulates adipocyte-induced fatty acid import and metabolism in breast cancer Gyamfi, Jones Yeo, Joo Hye Kwon, Doru Min, Byung Soh Cha, Yoon Jin Koo, Ja Seung Jeong, Joon Lee, Jinu Choi, Junjeong NPJ Breast Cancer Article Adipocytes influence breast cancer behaviour via fatty acid release into the tumour microenvironment. Co-culturing human adipocytes and breast cancer cells increased CD36 expression, with fatty acid import into breast cancer cells. Genetic ablation of CD36 attenuates adipocyte-induced epithelial-mesenchymal transition (EMT) and stemness. We show a feedforward loop between CD36 and STAT3; where CD36 activates STAT3 signalling and STAT3 binds to the CD36 promoter, regulating its expression. CD36 expression results in metabolic reprogramming, with a shift towards fatty acid oxidation. CD36 inhibition induces de novo lipogenesis in breast cancer cells. Increased CD36 expression occurs with increased FABP4 expression. We showed that CD36 directly interacts with FABP4 to regulate fatty acid import, transport, and metabolism. CD36 and FABP4 inhibition induces apoptosis in tumour cells. These results indicate that CD36 mediates fatty acid import from adipocytes into cancer cells and activates signalling pathways that drive tumour progression. Targeting CD36 may have a potential for therapy, which will target the tumour microenvironment. Nature Publishing Group UK 2021-09-24 /pmc/articles/PMC8463699/ /pubmed/34561446 http://dx.doi.org/10.1038/s41523-021-00324-7 Text en © The Author(s) 2021 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
Gyamfi, Jones
Yeo, Joo Hye
Kwon, Doru
Min, Byung Soh
Cha, Yoon Jin
Koo, Ja Seung
Jeong, Joon
Lee, Jinu
Choi, Junjeong
Interaction between CD36 and FABP4 modulates adipocyte-induced fatty acid import and metabolism in breast cancer
title Interaction between CD36 and FABP4 modulates adipocyte-induced fatty acid import and metabolism in breast cancer
title_full Interaction between CD36 and FABP4 modulates adipocyte-induced fatty acid import and metabolism in breast cancer
title_fullStr Interaction between CD36 and FABP4 modulates adipocyte-induced fatty acid import and metabolism in breast cancer
title_full_unstemmed Interaction between CD36 and FABP4 modulates adipocyte-induced fatty acid import and metabolism in breast cancer
title_short Interaction between CD36 and FABP4 modulates adipocyte-induced fatty acid import and metabolism in breast cancer
title_sort interaction between cd36 and fabp4 modulates adipocyte-induced fatty acid import and metabolism in breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463699/
https://www.ncbi.nlm.nih.gov/pubmed/34561446
http://dx.doi.org/10.1038/s41523-021-00324-7
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