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Published on: May 1, 2015
Myeloid Cells as Targets for Therapy in Solid Tumors
Tiziana Cotechini1, Terry R Medler, Lisa M Coussens
1From the *Department of Cell, Developmental & Cancer Biology and †Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Cancer progresses through interactions between tumor cells and host cells. Targeting myeloid cell programs shows promise for cancer immunotherapy by enhancing CD8 cytotoxic T cell immunity.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- Cancer development involves complex interactions between neoplastic cells and host cells within the tumor microenvironment.
- Myeloid cells, including macrophages, monocytes, dendritic cells, and granulocytes, are key components of the tumor microenvironment, often promoting tumor growth and suppressing anti-tumor immunity.
Purpose of the Study:
- To review the mechanisms by which myeloid cells are programmed to support tumor progression.
- To discuss the therapeutic potential of targeting these protumorigenic myeloid cell programs for cancer treatment.
Main Methods:
- This review synthesizes findings from preclinical studies and clinical evaluations of novel immune-based therapies.
- The focus is on understanding the molecular and cellular mechanisms driving myeloid cell involvement in cancer.
Main Results:
- Inhibition of critical myeloid-based programs has demonstrated tumor suppression in preclinical models.
- Targeting myeloid cell functions offers a strategy to overcome immune suppression within the tumor microenvironment.
Conclusions:
- Targeting protumorigenic myeloid cell programming is a promising strategy for cancer immunotherapy.
- Such approaches aim to attenuate solid tumor progression by inducing and mobilizing CD8 cytotoxic T cell immunity.
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