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Cellular senescence triggers intracellular acidification and lysosomal pH alkalinized via ATP6AP2 attenuation in breast cancer cells

Several chemotherapeutic drugs induce senescence in cancer cells; however, the mechanisms underlying intracellular pH dysregulation in senescent cells remain unclear. Adenosine triphosphatase H(+) transporting accessory protein 2 (ATP6AP2) plays a critical role in maintaining pH homeostasis in cellu...

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Autores principales: Li, Wei, Kawaguchi, Kosuke, Tanaka, Sunao, He, Chenfeng, Maeshima, Yurina, Suzuki, Eiji, Toi, Masakazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665353/
https://www.ncbi.nlm.nih.gov/pubmed/37993606
http://dx.doi.org/10.1038/s42003-023-05433-6
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author Li, Wei
Kawaguchi, Kosuke
Tanaka, Sunao
He, Chenfeng
Maeshima, Yurina
Suzuki, Eiji
Toi, Masakazu
author_facet Li, Wei
Kawaguchi, Kosuke
Tanaka, Sunao
He, Chenfeng
Maeshima, Yurina
Suzuki, Eiji
Toi, Masakazu
author_sort Li, Wei
collection PubMed
description Several chemotherapeutic drugs induce senescence in cancer cells; however, the mechanisms underlying intracellular pH dysregulation in senescent cells remain unclear. Adenosine triphosphatase H(+) transporting accessory protein 2 (ATP6AP2) plays a critical role in maintaining pH homeostasis in cellular compartments. Herein, we report the regulatory role of ATP6AP2 in senescent breast cancer cells treated with doxorubicin (Doxo) and abemaciclib (Abe). A decline in ATP6AP2 triggers aberrant pH levels that impair lysosomal function and cause immune profile changes in senescent breast cancer cells. Doxo and Abe elicited a stable senescent phenotype and altered the expression of senescence-related genes. Additionally, senescent cells show altered inflammatory and immune transcriptional profiles due to reprogramming of the senescence-associated secretory phenotype. These findings elucidate ATP6AP2-mediated cellular pH regulation and suggest a potential link in immune profile alteration during therapy-induced senescence in breast cancer cells, providing insights into the mechanisms involved in the senescence response to anticancer therapy.
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spelling pubmed-106653532023-11-22 Cellular senescence triggers intracellular acidification and lysosomal pH alkalinized via ATP6AP2 attenuation in breast cancer cells Li, Wei Kawaguchi, Kosuke Tanaka, Sunao He, Chenfeng Maeshima, Yurina Suzuki, Eiji Toi, Masakazu Commun Biol Article Several chemotherapeutic drugs induce senescence in cancer cells; however, the mechanisms underlying intracellular pH dysregulation in senescent cells remain unclear. Adenosine triphosphatase H(+) transporting accessory protein 2 (ATP6AP2) plays a critical role in maintaining pH homeostasis in cellular compartments. Herein, we report the regulatory role of ATP6AP2 in senescent breast cancer cells treated with doxorubicin (Doxo) and abemaciclib (Abe). A decline in ATP6AP2 triggers aberrant pH levels that impair lysosomal function and cause immune profile changes in senescent breast cancer cells. Doxo and Abe elicited a stable senescent phenotype and altered the expression of senescence-related genes. Additionally, senescent cells show altered inflammatory and immune transcriptional profiles due to reprogramming of the senescence-associated secretory phenotype. These findings elucidate ATP6AP2-mediated cellular pH regulation and suggest a potential link in immune profile alteration during therapy-induced senescence in breast cancer cells, providing insights into the mechanisms involved in the senescence response to anticancer therapy. Nature Publishing Group UK 2023-11-22 /pmc/articles/PMC10665353/ /pubmed/37993606 http://dx.doi.org/10.1038/s42003-023-05433-6 Text en © The Author(s) 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
Li, Wei
Kawaguchi, Kosuke
Tanaka, Sunao
He, Chenfeng
Maeshima, Yurina
Suzuki, Eiji
Toi, Masakazu
Cellular senescence triggers intracellular acidification and lysosomal pH alkalinized via ATP6AP2 attenuation in breast cancer cells
title Cellular senescence triggers intracellular acidification and lysosomal pH alkalinized via ATP6AP2 attenuation in breast cancer cells
title_full Cellular senescence triggers intracellular acidification and lysosomal pH alkalinized via ATP6AP2 attenuation in breast cancer cells
title_fullStr Cellular senescence triggers intracellular acidification and lysosomal pH alkalinized via ATP6AP2 attenuation in breast cancer cells
title_full_unstemmed Cellular senescence triggers intracellular acidification and lysosomal pH alkalinized via ATP6AP2 attenuation in breast cancer cells
title_short Cellular senescence triggers intracellular acidification and lysosomal pH alkalinized via ATP6AP2 attenuation in breast cancer cells
title_sort cellular senescence triggers intracellular acidification and lysosomal ph alkalinized via atp6ap2 attenuation in breast cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665353/
https://www.ncbi.nlm.nih.gov/pubmed/37993606
http://dx.doi.org/10.1038/s42003-023-05433-6
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