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Molecular characterization of renal cell carcinoma tumors from a phase III anti-angiogenic adjuvant therapy trial
Multigene assays can provide insight into key biological processes and prognostic information to guide development and selection of adjuvant cancer therapy. We report a comprehensive genomic and transcriptomic analysis of tumor samples from 171 patients at high risk for recurrent renal cell carcinom...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550765/ https://www.ncbi.nlm.nih.gov/pubmed/36216827 http://dx.doi.org/10.1038/s41467-022-33555-8 |
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author | Motzer, Robert J. Martini, Jean-François Mu, Xinmeng J. Staehler, Michael George, Daniel J. Valota, Olga Lin, Xun Pandha, Hardev S. Ching, Keith A. Ravaud, Alain |
author_facet | Motzer, Robert J. Martini, Jean-François Mu, Xinmeng J. Staehler, Michael George, Daniel J. Valota, Olga Lin, Xun Pandha, Hardev S. Ching, Keith A. Ravaud, Alain |
author_sort | Motzer, Robert J. |
collection | PubMed |
description | Multigene assays can provide insight into key biological processes and prognostic information to guide development and selection of adjuvant cancer therapy. We report a comprehensive genomic and transcriptomic analysis of tumor samples from 171 patients at high risk for recurrent renal cell carcinoma post nephrectomy from the S-TRAC trial (NCT00375674). We identify gene expression signatures, including STRAC11 (derived from the sunitinib-treated population). The overlap in key elements captured in these gene expression signatures, which include genes representative of the tumor stroma microenvironment, regulatory T cell, and myeloid cells, suggests they are likely to be both prognostic and predictive of the anti-angiogenic effect in the adjuvant setting. These signatures also point to the identification of potential therapeutic targets for development in adjuvant renal cell carcinoma, such as MERTK and TDO2. Finally, our findings suggest that while anti-angiogenic adjuvant therapy might be important, it may not be sufficient to prevent recurrence and that other factors such as immune response and tumor environment may be of greater importance. |
format | Online Article Text |
id | pubmed-9550765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95507652022-10-12 Molecular characterization of renal cell carcinoma tumors from a phase III anti-angiogenic adjuvant therapy trial Motzer, Robert J. Martini, Jean-François Mu, Xinmeng J. Staehler, Michael George, Daniel J. Valota, Olga Lin, Xun Pandha, Hardev S. Ching, Keith A. Ravaud, Alain Nat Commun Article Multigene assays can provide insight into key biological processes and prognostic information to guide development and selection of adjuvant cancer therapy. We report a comprehensive genomic and transcriptomic analysis of tumor samples from 171 patients at high risk for recurrent renal cell carcinoma post nephrectomy from the S-TRAC trial (NCT00375674). We identify gene expression signatures, including STRAC11 (derived from the sunitinib-treated population). The overlap in key elements captured in these gene expression signatures, which include genes representative of the tumor stroma microenvironment, regulatory T cell, and myeloid cells, suggests they are likely to be both prognostic and predictive of the anti-angiogenic effect in the adjuvant setting. These signatures also point to the identification of potential therapeutic targets for development in adjuvant renal cell carcinoma, such as MERTK and TDO2. Finally, our findings suggest that while anti-angiogenic adjuvant therapy might be important, it may not be sufficient to prevent recurrence and that other factors such as immune response and tumor environment may be of greater importance. Nature Publishing Group UK 2022-10-10 /pmc/articles/PMC9550765/ /pubmed/36216827 http://dx.doi.org/10.1038/s41467-022-33555-8 Text en © The Author(s) 2022 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 Motzer, Robert J. Martini, Jean-François Mu, Xinmeng J. Staehler, Michael George, Daniel J. Valota, Olga Lin, Xun Pandha, Hardev S. Ching, Keith A. Ravaud, Alain Molecular characterization of renal cell carcinoma tumors from a phase III anti-angiogenic adjuvant therapy trial |
title | Molecular characterization of renal cell carcinoma tumors from a phase III anti-angiogenic adjuvant therapy trial |
title_full | Molecular characterization of renal cell carcinoma tumors from a phase III anti-angiogenic adjuvant therapy trial |
title_fullStr | Molecular characterization of renal cell carcinoma tumors from a phase III anti-angiogenic adjuvant therapy trial |
title_full_unstemmed | Molecular characterization of renal cell carcinoma tumors from a phase III anti-angiogenic adjuvant therapy trial |
title_short | Molecular characterization of renal cell carcinoma tumors from a phase III anti-angiogenic adjuvant therapy trial |
title_sort | molecular characterization of renal cell carcinoma tumors from a phase iii anti-angiogenic adjuvant therapy trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550765/ https://www.ncbi.nlm.nih.gov/pubmed/36216827 http://dx.doi.org/10.1038/s41467-022-33555-8 |
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