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Characterization of the role of TMEM45A in cancer cell sensitivity to cisplatin

TMEM45A is a transmembrane protein involved in tumor progression and cancer resistance to chemotherapeutic agents in hypoxic condition. It is correlated to a low breast cancer patient overall survival. However, little is known about this protein, in particular the mechanisms by which TMEM45A modulat...

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Autores principales: Schmit, Kathleen, Chen, Jia-Wei, Ayama-Canden, Sophie, Fransolet, Maude, Finet, Laure, Demazy, Catherine, D’Hondt, Lionel, Graux, Carlos, Michiels, Carine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892797/
https://www.ncbi.nlm.nih.gov/pubmed/31801939
http://dx.doi.org/10.1038/s41419-019-2088-x
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author Schmit, Kathleen
Chen, Jia-Wei
Ayama-Canden, Sophie
Fransolet, Maude
Finet, Laure
Demazy, Catherine
D’Hondt, Lionel
Graux, Carlos
Michiels, Carine
author_facet Schmit, Kathleen
Chen, Jia-Wei
Ayama-Canden, Sophie
Fransolet, Maude
Finet, Laure
Demazy, Catherine
D’Hondt, Lionel
Graux, Carlos
Michiels, Carine
author_sort Schmit, Kathleen
collection PubMed
description TMEM45A is a transmembrane protein involved in tumor progression and cancer resistance to chemotherapeutic agents in hypoxic condition. It is correlated to a low breast cancer patient overall survival. However, little is known about this protein, in particular the mechanisms by which TMEM45A modulates cancer cell chemosensitivity. In this work, the messenger RNA expression of TMEM45A was assessed in head and neck squamous cell carcinoma (HNSCC) and renal cell carcinoma (RCC) biopsies. TMEM45A was upregulated in patients diagnosed for head and neck or renal cancer. Then, the implication of this protein in cisplatin sensitivity was explored in SQD9 and RCC4 + pVHL cells. TMEM45A inactivation decreased cell proliferation and modulated cell responses to cisplatin. Indeed, TMEM45A inactivation increased the sensitivity of SQD9 cells to cisplatin, whereas it rendered RCC4 + pVHL cells resistant to this anticancer agent. Through RNA-sequencing analysis, we identified several deregulated pathways that indicated that the impact on cisplatin sensitivity may be associated to the inhibition of DNA damage repair and to UPR pathway activation. This study demonstrated, for the first time, an anti or a pro-apoptotic role of this protein depending on the cancer type and highlighted the role of TMEM45A in modulating patient responses to treatment.
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spelling pubmed-68927972019-12-05 Characterization of the role of TMEM45A in cancer cell sensitivity to cisplatin Schmit, Kathleen Chen, Jia-Wei Ayama-Canden, Sophie Fransolet, Maude Finet, Laure Demazy, Catherine D’Hondt, Lionel Graux, Carlos Michiels, Carine Cell Death Dis Article TMEM45A is a transmembrane protein involved in tumor progression and cancer resistance to chemotherapeutic agents in hypoxic condition. It is correlated to a low breast cancer patient overall survival. However, little is known about this protein, in particular the mechanisms by which TMEM45A modulates cancer cell chemosensitivity. In this work, the messenger RNA expression of TMEM45A was assessed in head and neck squamous cell carcinoma (HNSCC) and renal cell carcinoma (RCC) biopsies. TMEM45A was upregulated in patients diagnosed for head and neck or renal cancer. Then, the implication of this protein in cisplatin sensitivity was explored in SQD9 and RCC4 + pVHL cells. TMEM45A inactivation decreased cell proliferation and modulated cell responses to cisplatin. Indeed, TMEM45A inactivation increased the sensitivity of SQD9 cells to cisplatin, whereas it rendered RCC4 + pVHL cells resistant to this anticancer agent. Through RNA-sequencing analysis, we identified several deregulated pathways that indicated that the impact on cisplatin sensitivity may be associated to the inhibition of DNA damage repair and to UPR pathway activation. This study demonstrated, for the first time, an anti or a pro-apoptotic role of this protein depending on the cancer type and highlighted the role of TMEM45A in modulating patient responses to treatment. Nature Publishing Group UK 2019-12-04 /pmc/articles/PMC6892797/ /pubmed/31801939 http://dx.doi.org/10.1038/s41419-019-2088-x Text en © The Author(s) 2019 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
Schmit, Kathleen
Chen, Jia-Wei
Ayama-Canden, Sophie
Fransolet, Maude
Finet, Laure
Demazy, Catherine
D’Hondt, Lionel
Graux, Carlos
Michiels, Carine
Characterization of the role of TMEM45A in cancer cell sensitivity to cisplatin
title Characterization of the role of TMEM45A in cancer cell sensitivity to cisplatin
title_full Characterization of the role of TMEM45A in cancer cell sensitivity to cisplatin
title_fullStr Characterization of the role of TMEM45A in cancer cell sensitivity to cisplatin
title_full_unstemmed Characterization of the role of TMEM45A in cancer cell sensitivity to cisplatin
title_short Characterization of the role of TMEM45A in cancer cell sensitivity to cisplatin
title_sort characterization of the role of tmem45a in cancer cell sensitivity to cisplatin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892797/
https://www.ncbi.nlm.nih.gov/pubmed/31801939
http://dx.doi.org/10.1038/s41419-019-2088-x
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