Human lung cancer-derived mesenchymal stem cells promote tumor growth and immunosuppression
- Xiaoyan Gao 1, He Ren 1, Zhengrong Zhang 1,2, Shuai Cao 3, Bo Zhang 1,4, Qiang Sun 4, Gerry Melino 2,5, Hongyan Huang 6
- Xiaoyan Gao 1, He Ren 1, Zhengrong Zhang 1,2
- 1Department of Oncology, Beijing Shijitan Hospital of Capital Medical University, 10 Tieyi Road, Beijing, 100038, China.
- 2Department of Experimental Medicine, TOR, University of Rome "Tor Vergata", Rome, Italy.
- 3Department of Orthopedics, Civil Aviation General Hospital, No.1 Gaojing Street, Chaoyang District, Beijing, 100123, China.
- 4Laboratory of Cell Engineering, Institute of Biotechnology, Beijing, China.
- 5DZNE German Center for Neurodegenerative Diseases, Bonn, Germany.
- 6Department of Oncology, Beijing Shijitan Hospital of Capital Medical University, 10 Tieyi Road, Beijing, 100038, China. huangh1975@mail.ccmu.edu.cn.
- 0Department of Oncology, Beijing Shijitan Hospital of Capital Medical University, 10 Tieyi Road, Beijing, 100038, China.
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View abstract on PubMed
Summary
This summary is machine-generated.Mesenchymal stem cells from lung cancer enhance tumor growth and protect cancer cells from immune attack by natural killer and T cells, hindering antitumor responses.
Area Of Science
- Oncology
- Immunology
- Stem Cell Biology
Background
- Mesenchymal stem cells (MSCs) are found in solid tumors, influencing the tumor microenvironment.
- Their precise role in cancer progression remains incompletely understood.
Purpose Of The Study
- To investigate the function of MSCs isolated from non-small cell lung cancer (NSCLC) tissues.
- To determine the impact of these MSCs on tumor growth and immune surveillance.
Main Methods
- Isolation and characterization of MSCs from human NSCLC tumor tissues.
- Assessment of MSC morphology, immunophenotype, tumorigenicity, and differentiation potential.
- In vivo studies evaluating the effect of MSCs on tumor growth and immune cell activity (natural killer cells and T cells).
Main Results
- Lung cancer-derived MSCs exhibited typical MSC characteristics and were nontumorigenic with multipotent differentiation capacity.
- Co-culturing tumor cells with these MSCs significantly enhanced tumor growth in vivo.
- MSCs markedly inhibited the cytotoxic activity of natural killer (NK) cells and activated T cells against tumor cells.
Conclusions
- Human lung cancer-derived MSCs promote tumor progression.
- These MSCs shield tumor cells from immune destruction by suppressing the antitumor functions of NK and T cells.
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