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CMTM6 and CMTM7: New leads for PD‐L1 regulation in breast cancer cells undergoing EMT

Programmed death‐ligand 1 (PD‐L1) expression has long been used as a biomarker to stratify patients with cancer who will benefit from anti‐PD‐1/PD‐L1 immunotherapy. However, the use of PD‐L1 as a biomarker to guide treatment decisions has recently been called into question due to its dynamic and het...

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Detalles Bibliográficos
Autores principales: Xiao, Malina, Duhem, Caroline, Chammout, Anwar, Berchem, Guy, Janji, Bassam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325512/
https://www.ncbi.nlm.nih.gov/pubmed/35575054
http://dx.doi.org/10.1002/jcb.30273
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author Xiao, Malina
Duhem, Caroline
Chammout, Anwar
Berchem, Guy
Janji, Bassam
author_facet Xiao, Malina
Duhem, Caroline
Chammout, Anwar
Berchem, Guy
Janji, Bassam
author_sort Xiao, Malina
collection PubMed
description Programmed death‐ligand 1 (PD‐L1) expression has long been used as a biomarker to stratify patients with cancer who will benefit from anti‐PD‐1/PD‐L1 immunotherapy. However, the use of PD‐L1 as a biomarker to guide treatment decisions has recently been called into question due to its dynamic and heterogeneous expression within each tumor and among different tumors as well as during tumor cell plasticity. Therefore, understanding the molecular basis of PD‐L1 expression would enable delineating its value as a reliable biomarker in the clinic. Here, we provide our perspective on the involvement of CMTM6 and CMTM7 as new lead candidates for the regulation of PD‐L1 in breast tumors undergoing an epithelial to mesenchymal transition.
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spelling pubmed-93255122022-07-30 CMTM6 and CMTM7: New leads for PD‐L1 regulation in breast cancer cells undergoing EMT Xiao, Malina Duhem, Caroline Chammout, Anwar Berchem, Guy Janji, Bassam J Cell Biochem Viewpoint Programmed death‐ligand 1 (PD‐L1) expression has long been used as a biomarker to stratify patients with cancer who will benefit from anti‐PD‐1/PD‐L1 immunotherapy. However, the use of PD‐L1 as a biomarker to guide treatment decisions has recently been called into question due to its dynamic and heterogeneous expression within each tumor and among different tumors as well as during tumor cell plasticity. Therefore, understanding the molecular basis of PD‐L1 expression would enable delineating its value as a reliable biomarker in the clinic. Here, we provide our perspective on the involvement of CMTM6 and CMTM7 as new lead candidates for the regulation of PD‐L1 in breast tumors undergoing an epithelial to mesenchymal transition. John Wiley and Sons Inc. 2022-05-16 2022-06 /pmc/articles/PMC9325512/ /pubmed/35575054 http://dx.doi.org/10.1002/jcb.30273 Text en © 2022 The Authors. Journal of Cellular Biochemistry published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Viewpoint
Xiao, Malina
Duhem, Caroline
Chammout, Anwar
Berchem, Guy
Janji, Bassam
CMTM6 and CMTM7: New leads for PD‐L1 regulation in breast cancer cells undergoing EMT
title CMTM6 and CMTM7: New leads for PD‐L1 regulation in breast cancer cells undergoing EMT
title_full CMTM6 and CMTM7: New leads for PD‐L1 regulation in breast cancer cells undergoing EMT
title_fullStr CMTM6 and CMTM7: New leads for PD‐L1 regulation in breast cancer cells undergoing EMT
title_full_unstemmed CMTM6 and CMTM7: New leads for PD‐L1 regulation in breast cancer cells undergoing EMT
title_short CMTM6 and CMTM7: New leads for PD‐L1 regulation in breast cancer cells undergoing EMT
title_sort cmtm6 and cmtm7: new leads for pd‐l1 regulation in breast cancer cells undergoing emt
topic Viewpoint
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325512/
https://www.ncbi.nlm.nih.gov/pubmed/35575054
http://dx.doi.org/10.1002/jcb.30273
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