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Dual functions of angiopoietin-like protein 2 signaling in tumor progression and anti-tumor immunity
Angiopoietin-like protein 2 (ANGPTL2) is a secreted glycoprotein homologous to angiopoietins. Previous studies suggest that tumor cell-derived ANGPTL2 has tumor-promoting function. Here, we conducted mechanistic analysis comparing ANGPTL2 function in cancer progression in a murine syngeneic model of...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942048/ https://www.ncbi.nlm.nih.gov/pubmed/31727773 http://dx.doi.org/10.1101/gad.329417.119 |
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author | Horiguchi, Haruki Kadomatsu, Tsuyoshi Kurahashi, Ryoma Hara, Chiaki Miyata, Keishi Baba, Masaya Osumi, Hironobu Terada, Kazutoyo Araki, Kimi Takai, Toshiyuki Kamba, Tomomi Linehan, W. Marston Moroishi, Toshiro Oike, Yuichi |
author_facet | Horiguchi, Haruki Kadomatsu, Tsuyoshi Kurahashi, Ryoma Hara, Chiaki Miyata, Keishi Baba, Masaya Osumi, Hironobu Terada, Kazutoyo Araki, Kimi Takai, Toshiyuki Kamba, Tomomi Linehan, W. Marston Moroishi, Toshiro Oike, Yuichi |
author_sort | Horiguchi, Haruki |
collection | PubMed |
description | Angiopoietin-like protein 2 (ANGPTL2) is a secreted glycoprotein homologous to angiopoietins. Previous studies suggest that tumor cell-derived ANGPTL2 has tumor-promoting function. Here, we conducted mechanistic analysis comparing ANGPTL2 function in cancer progression in a murine syngeneic model of melanoma and a mouse model of translocation renal cell carcinoma (tRCC). ANGPTL2 deficiency in tumor cells slowed tRCC progression, supporting a tumor-promoting role. However, systemic ablation of ANGPTL2 accelerated tRCC progression, supporting a tumor-suppressing role. The syngeneic model also demonstrated a tumor-suppressing role of ANGPTL2 in host tumor microenvironmental cells. Furthermore, the syngeneic model showed that PDGFRα(+) fibroblasts in the tumor microenvironment express abundant ANGPTL2 and contribute to tumor suppression. Moreover, host ANGPTL2 facilitates CD8(+) T-cell cross-priming and enhances anti-tumor immune responses. Importantly, ANGPTL2 activates dendritic cells through PIR-B–NOTCH signaling and enhances tumor vaccine efficacy. Our study provides strong evidence that ANGPTL2 can function in either tumor promotion or suppression, depending on what cell type it is expressed in. |
format | Online Article Text |
id | pubmed-6942048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-69420482020-06-01 Dual functions of angiopoietin-like protein 2 signaling in tumor progression and anti-tumor immunity Horiguchi, Haruki Kadomatsu, Tsuyoshi Kurahashi, Ryoma Hara, Chiaki Miyata, Keishi Baba, Masaya Osumi, Hironobu Terada, Kazutoyo Araki, Kimi Takai, Toshiyuki Kamba, Tomomi Linehan, W. Marston Moroishi, Toshiro Oike, Yuichi Genes Dev Research Paper Angiopoietin-like protein 2 (ANGPTL2) is a secreted glycoprotein homologous to angiopoietins. Previous studies suggest that tumor cell-derived ANGPTL2 has tumor-promoting function. Here, we conducted mechanistic analysis comparing ANGPTL2 function in cancer progression in a murine syngeneic model of melanoma and a mouse model of translocation renal cell carcinoma (tRCC). ANGPTL2 deficiency in tumor cells slowed tRCC progression, supporting a tumor-promoting role. However, systemic ablation of ANGPTL2 accelerated tRCC progression, supporting a tumor-suppressing role. The syngeneic model also demonstrated a tumor-suppressing role of ANGPTL2 in host tumor microenvironmental cells. Furthermore, the syngeneic model showed that PDGFRα(+) fibroblasts in the tumor microenvironment express abundant ANGPTL2 and contribute to tumor suppression. Moreover, host ANGPTL2 facilitates CD8(+) T-cell cross-priming and enhances anti-tumor immune responses. Importantly, ANGPTL2 activates dendritic cells through PIR-B–NOTCH signaling and enhances tumor vaccine efficacy. Our study provides strong evidence that ANGPTL2 can function in either tumor promotion or suppression, depending on what cell type it is expressed in. Cold Spring Harbor Laboratory Press 2019-12-01 /pmc/articles/PMC6942048/ /pubmed/31727773 http://dx.doi.org/10.1101/gad.329417.119 Text en © 2019 Horiguchi et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Paper Horiguchi, Haruki Kadomatsu, Tsuyoshi Kurahashi, Ryoma Hara, Chiaki Miyata, Keishi Baba, Masaya Osumi, Hironobu Terada, Kazutoyo Araki, Kimi Takai, Toshiyuki Kamba, Tomomi Linehan, W. Marston Moroishi, Toshiro Oike, Yuichi Dual functions of angiopoietin-like protein 2 signaling in tumor progression and anti-tumor immunity |
title | Dual functions of angiopoietin-like protein 2 signaling in tumor progression and anti-tumor immunity |
title_full | Dual functions of angiopoietin-like protein 2 signaling in tumor progression and anti-tumor immunity |
title_fullStr | Dual functions of angiopoietin-like protein 2 signaling in tumor progression and anti-tumor immunity |
title_full_unstemmed | Dual functions of angiopoietin-like protein 2 signaling in tumor progression and anti-tumor immunity |
title_short | Dual functions of angiopoietin-like protein 2 signaling in tumor progression and anti-tumor immunity |
title_sort | dual functions of angiopoietin-like protein 2 signaling in tumor progression and anti-tumor immunity |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942048/ https://www.ncbi.nlm.nih.gov/pubmed/31727773 http://dx.doi.org/10.1101/gad.329417.119 |
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