CD39/CD73 upregulation on myeloid-derived suppressor cells via TGF-β-mTOR-HIF-1 signaling in patients with non-small cell lung cancer
Title: | CD39/CD73 upregulation on myeloid-derived suppressor cells via TGF-β-mTOR-HIF-1 signaling in patients with non-small cell lung cancer |
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Authors: | Jieyao Li, Liping Wang, Xinfeng Chen, Lifeng Li, Yu Li, Yu Ping, Lan Huang, Dongli Yue, Zhen Zhang, Fei Wang, Feng Li, Li Yang, Jianmin Huang, Shuangning Yang, Hong Li, Xuan Zhao, Wenjie Dong, Yan Yan, Song Zhao, Bo Huang, Bin Zhang, Yi Zhang |
Source: | OncoImmunology, Vol 6, Iss 6 (2017) |
Publisher Information: | Taylor & Francis Group, 2017. |
Publication Year: | 2017 |
Collection: | LCC:Immunologic diseases. Allergy LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens |
Subject Terms: | cd39, cd73, mdscs, nsclc, tgf-β, Immunologic diseases. Allergy, RC581-607, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282 |
More Details: | CD39/CD73-adenosine pathway has been recently defined as an important tumor-induced immunosuppressive mechanism. We here documented a fraction of CD11b+CD33+ myeloid-derived suppressor cells (MDSCs) in peripheral blood and tumor tissues from non-small cell lung cancer (NSCLC) patients expressed surface ectonucleotidases CD39 and CD73. Tumor TGF-β stimulated CD39 and CD73 expression, thereby inhibited T cell and NK cell activity, and protected tumor cells from the cytotoxic effect of chemotherapy through ectonucleotidase activity. Mechanistically, TGF-β triggered phosphorylation of mammalian target of rapamycin, and subsequently activated hypoxia-inducible factor-1α (HIF-1α) that induced CD39/CD73 expression on MDSCs. CD39 and CD73 on MDSCs, therefore, link their immunosuppressive and chemo-protective effects to NSCLC progression, providing novel targets for chemo-immunotherapeutic intervention. |
Document Type: | article |
File Description: | electronic resource |
Language: | English |
ISSN: | 2162-402X 2162402X |
Relation: | https://doaj.org/toc/2162-402X |
DOI: | 10.1080/2162402X.2017.1320011 |
Access URL: | https://doaj.org/article/cc2d10487b184685a0a822bc1381edf1 |
Accession Number: | edsdoj.2d10487b184685a0a822bc1381edf1 |
Database: | Directory of Open Access Journals |
ISSN: | 2162402X |
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DOI: | 10.1080/2162402X.2017.1320011 |
Published in: | OncoImmunology |
Language: | English |