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Vestigial-like 1 is a shared targetable cancer-placenta antigen expressed by pancreatic and basal-like breast cancers

Cytotoxic T lymphocyte (CTL)-based cancer immunotherapies have shown great promise for inducing clinical regressions by targeting tumor-associated antigens (TAA). To expand the TAA landscape of pancreatic ductal adenocarcinoma (PDAC), we performed tandem mass spectrometry analysis of HLA class I-bou...

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Autores principales: Bradley, Sherille D., Talukder, Amjad H., Lai, Ivy, Davis, Rebecca, Alvarez, Hector, Tiriac, Herve, Zhang, Minying, Chiu, Yulun, Melendez, Brenda, Jackson, Kyle R., Katailiha, Arjun, Sonnemann, Heather M., Li, Fenge, Kang, Yaan, Qiao, Na, Pan, Bih-Fang, Lorenzi, Philip L., Hurd, Mark, Mittendorf, Elizabeth A., Peterson, Christine B., Javle, Milind, Bristow, Christopher, Kim, Michael, Tuveson, David A., Hawke, David, Kopetz, Scott, Wolff, Robert A., Hwu, Patrick, Maitra, Anirban, Roszik, Jason, Yee, Cassian, Lizée, Gregory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577998/
https://www.ncbi.nlm.nih.gov/pubmed/33087697
http://dx.doi.org/10.1038/s41467-020-19141-w
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author Bradley, Sherille D.
Talukder, Amjad H.
Lai, Ivy
Davis, Rebecca
Alvarez, Hector
Tiriac, Herve
Zhang, Minying
Chiu, Yulun
Melendez, Brenda
Jackson, Kyle R.
Katailiha, Arjun
Sonnemann, Heather M.
Li, Fenge
Kang, Yaan
Qiao, Na
Pan, Bih-Fang
Lorenzi, Philip L.
Hurd, Mark
Mittendorf, Elizabeth A.
Peterson, Christine B.
Javle, Milind
Bristow, Christopher
Kim, Michael
Tuveson, David A.
Hawke, David
Kopetz, Scott
Wolff, Robert A.
Hwu, Patrick
Maitra, Anirban
Roszik, Jason
Yee, Cassian
Lizée, Gregory
author_facet Bradley, Sherille D.
Talukder, Amjad H.
Lai, Ivy
Davis, Rebecca
Alvarez, Hector
Tiriac, Herve
Zhang, Minying
Chiu, Yulun
Melendez, Brenda
Jackson, Kyle R.
Katailiha, Arjun
Sonnemann, Heather M.
Li, Fenge
Kang, Yaan
Qiao, Na
Pan, Bih-Fang
Lorenzi, Philip L.
Hurd, Mark
Mittendorf, Elizabeth A.
Peterson, Christine B.
Javle, Milind
Bristow, Christopher
Kim, Michael
Tuveson, David A.
Hawke, David
Kopetz, Scott
Wolff, Robert A.
Hwu, Patrick
Maitra, Anirban
Roszik, Jason
Yee, Cassian
Lizée, Gregory
author_sort Bradley, Sherille D.
collection PubMed
description Cytotoxic T lymphocyte (CTL)-based cancer immunotherapies have shown great promise for inducing clinical regressions by targeting tumor-associated antigens (TAA). To expand the TAA landscape of pancreatic ductal adenocarcinoma (PDAC), we performed tandem mass spectrometry analysis of HLA class I-bound peptides from 35 PDAC patient tumors. This identified a shared HLA-A*0101 restricted peptide derived from co-transcriptional activator Vestigial-like 1 (VGLL1) as a putative TAA demonstrating overexpression in multiple tumor types and low or absent expression in essential normal tissues. Here we show that VGLL1-specific CTLs expanded from the blood of a PDAC patient could recognize and kill in an antigen-specific manner a majority of HLA-A*0101 allogeneic tumor cell lines derived not only from PDAC, but also bladder, ovarian, gastric, lung, and basal-like breast cancers. Gene expression profiling reveals VGLL1 as a member of a unique group of cancer-placenta antigens (CPA) that may constitute immunotherapeutic targets for patients with multiple cancer types.
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spelling pubmed-75779982020-10-29 Vestigial-like 1 is a shared targetable cancer-placenta antigen expressed by pancreatic and basal-like breast cancers Bradley, Sherille D. Talukder, Amjad H. Lai, Ivy Davis, Rebecca Alvarez, Hector Tiriac, Herve Zhang, Minying Chiu, Yulun Melendez, Brenda Jackson, Kyle R. Katailiha, Arjun Sonnemann, Heather M. Li, Fenge Kang, Yaan Qiao, Na Pan, Bih-Fang Lorenzi, Philip L. Hurd, Mark Mittendorf, Elizabeth A. Peterson, Christine B. Javle, Milind Bristow, Christopher Kim, Michael Tuveson, David A. Hawke, David Kopetz, Scott Wolff, Robert A. Hwu, Patrick Maitra, Anirban Roszik, Jason Yee, Cassian Lizée, Gregory Nat Commun Article Cytotoxic T lymphocyte (CTL)-based cancer immunotherapies have shown great promise for inducing clinical regressions by targeting tumor-associated antigens (TAA). To expand the TAA landscape of pancreatic ductal adenocarcinoma (PDAC), we performed tandem mass spectrometry analysis of HLA class I-bound peptides from 35 PDAC patient tumors. This identified a shared HLA-A*0101 restricted peptide derived from co-transcriptional activator Vestigial-like 1 (VGLL1) as a putative TAA demonstrating overexpression in multiple tumor types and low or absent expression in essential normal tissues. Here we show that VGLL1-specific CTLs expanded from the blood of a PDAC patient could recognize and kill in an antigen-specific manner a majority of HLA-A*0101 allogeneic tumor cell lines derived not only from PDAC, but also bladder, ovarian, gastric, lung, and basal-like breast cancers. Gene expression profiling reveals VGLL1 as a member of a unique group of cancer-placenta antigens (CPA) that may constitute immunotherapeutic targets for patients with multiple cancer types. Nature Publishing Group UK 2020-10-21 /pmc/articles/PMC7577998/ /pubmed/33087697 http://dx.doi.org/10.1038/s41467-020-19141-w Text en © The Author(s) 2020 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
Bradley, Sherille D.
Talukder, Amjad H.
Lai, Ivy
Davis, Rebecca
Alvarez, Hector
Tiriac, Herve
Zhang, Minying
Chiu, Yulun
Melendez, Brenda
Jackson, Kyle R.
Katailiha, Arjun
Sonnemann, Heather M.
Li, Fenge
Kang, Yaan
Qiao, Na
Pan, Bih-Fang
Lorenzi, Philip L.
Hurd, Mark
Mittendorf, Elizabeth A.
Peterson, Christine B.
Javle, Milind
Bristow, Christopher
Kim, Michael
Tuveson, David A.
Hawke, David
Kopetz, Scott
Wolff, Robert A.
Hwu, Patrick
Maitra, Anirban
Roszik, Jason
Yee, Cassian
Lizée, Gregory
Vestigial-like 1 is a shared targetable cancer-placenta antigen expressed by pancreatic and basal-like breast cancers
title Vestigial-like 1 is a shared targetable cancer-placenta antigen expressed by pancreatic and basal-like breast cancers
title_full Vestigial-like 1 is a shared targetable cancer-placenta antigen expressed by pancreatic and basal-like breast cancers
title_fullStr Vestigial-like 1 is a shared targetable cancer-placenta antigen expressed by pancreatic and basal-like breast cancers
title_full_unstemmed Vestigial-like 1 is a shared targetable cancer-placenta antigen expressed by pancreatic and basal-like breast cancers
title_short Vestigial-like 1 is a shared targetable cancer-placenta antigen expressed by pancreatic and basal-like breast cancers
title_sort vestigial-like 1 is a shared targetable cancer-placenta antigen expressed by pancreatic and basal-like breast cancers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577998/
https://www.ncbi.nlm.nih.gov/pubmed/33087697
http://dx.doi.org/10.1038/s41467-020-19141-w
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