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Myeloid-derived suppressor cells in colorectal cancer: prognostic biomarkers and therapeutic targets

Al-Mterin, MA; Elkord, E

Myeloid-derived suppressor cells in colorectal cancer: prognostic biomarkers and therapeutic targets Thumbnail


Authors

MA Al-Mterin

E Elkord



Abstract

Myeloid-derived suppressor cells (MDSCs) are a group of immature myeloid cells, which are expanded in most cancer patients. MDSCs suppress host immune responses, leading to cancer growth and progression. Several studies demonstrated that there was a relationship between levels of MDSCs and tumorigenesis in colorectal cancer (CRC) patients. MDSCs are now being investigated for their role as possible therapeutic targets in cancer treatment. This review summarizes available studies that investigated MDSC expansion in CRC patients, as well as their role in CRC tumorigenesis, prognosis, and targeting. Based on the available studies, there is a possible relationship between high levels of MDSCs and CRC progression. Additionally, targeting MDSCs in CRC patients selectively represents a significant challenge for the development of targeted treatments. Targeting of MDSCs could be exploited in different ways including MDSC depletion, inhibition of MDSC function and recruitment, and enhancing MDSC differentiation. Overall, MDSCs could be exploited as prognostic biomarkers and potential therapeutic targets in CRC. [Abstract copyright: © The Author(s) 2022.]

Citation

Al-Mterin, M., & Elkord, E. (2022). Myeloid-derived suppressor cells in colorectal cancer: prognostic biomarkers and therapeutic targets. Exploration of Targeted Anti-tumor Therapy, 3(4), 497-510. https://doi.org/10.37349/etat.2022.00097

Journal Article Type Article
Acceptance Date Jul 20, 2022
Publication Date Aug 31, 2022
Deposit Date Oct 10, 2022
Publicly Available Date Oct 10, 2022
Journal Exploration of targeted anti-tumor therapy
Print ISSN 2692-3114
Publisher Open Exploration
Volume 3
Issue 4
Pages 497-510
DOI https://doi.org/10.37349/etat.2022.00097
Publisher URL https://doi.org/10.37349/etat.2022.00097

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