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Published on: October 20, 2016
Hostile takeover: glioma stem cells recruit TAMs to support tumor progression
Yu Shi1, Yi-fang Ping1, Xia Zhang1
1Institute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University, Chongqing 400038, China; Key Laboratory of Tumor Immunopathology of Ministry of Education of China, Third Military Medical University, Chongqing 400038, China.
Abstract:
The dynamic interaction between cancer cells and immune cells is a critical concern for developing effective tumor immunotherapies. In a recent issue of Nature Cell Biology, Zhou et al. (2015) report that glioma stem cells secrete Periostin (POSTN), which recruits tumor-associated macrophages (TAMs) and supports the tumor-promoting M2 subtype.
Insights
Glioma stem cells secrete Periostin (POSTN), attracting tumor-associated macrophages (TAMs). This interaction promotes the M2 subtype, crucial for understanding tumor immunotherapy development.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- The interaction between cancer and immune cells is vital for effective tumor immunotherapies.
- Glioma stem cells (GSCs) play a significant role in tumor progression and immune evasion.
Purpose of the Study:
- To investigate the role of glioma stem cells in recruiting immune cells.
- To identify specific molecules secreted by GSCs that influence the tumor microenvironment.
Main Methods:
- Analysis of gene expression in glioma stem cells.
- Immunohistochemistry to detect Periostin and macrophage markers in tumor tissues.
- Co-culture experiments to assess the effect of GSC-secreted factors on macrophage polarization.
Main Results:
- Glioma stem cells were found to secrete Periostin (POSTN).
- Periostin was shown to recruit tumor-associated macrophages (TAMs) to the tumor site.
- Recruited TAMs were predominantly of the M2 subtype, which is associated with tumor promotion.
Conclusions:
- Glioma stem cells utilize Periostin to shape the immune microenvironment.
- The POSTN-mediated recruitment of M2 TAMs by GSCs represents a potential therapeutic target for glioma immunotherapy.
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