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Cordycepin Remodels the Tumor Microenvironment of Colorectal Cancer by Down-regulating the Expression of PD-L1

Overview
Specialty Oncology
Date 2023 Nov 1
PMID 37910234
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Abstract

Purpose: Colorectal cancer, as a common malignant tumor, poses a serious threat to human life. Cordycepin, derived from Cordyceps militaris extract, which was established as a capable inhibitor of tumor growth. Nevertheless, the precise antitumor mechanism of cordycepin in colorectal cancer cells remains elusive.

Methods: Herein, our initial focus was to explore the tumor-suppressive impact of cordycepin through its influence on various biological functions in murine colorectal cancer cells, conducted by an in vitro setting. First, we investigated the tumor-suppressive effect of cordycepin on the regulation of biological functions in murine colorectal cancer cells in vitro. Furthermore, we evaluated the in vivo antitumor potential of cordycepin using a mouse preclinical tumor model, and further explored the antitumor mechanism.

Results: Our findings revealed that cordycepin effectively inhibit the proliferation, invasion, and migration of murine colon cancer cells. Moreover, there is a substantial reduction in the expression of PD-L1 observed in tumor cells, in response to cordycepin treatment. Collectively, these results demonstrate the significant tumor-suppressive attributes of cordycepin against colorectal cancer. Consequently, our study lays a solid foundation for the potential clinical utilization of cordycepin in cancer therapy.

Conclusion: Cordycepin inhibits the biological functions of colorectal cancer cells and suppresses tumor growth by reducing the expression of PD-L1.

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References
1.
AlMusawi S, Ahmed M, Nateri A . Understanding cell-cell communication and signaling in the colorectal cancer microenvironment. Clin Transl Med. 2021; 11(2):e308. PMC: 7868082. DOI: 10.1002/ctm2.308. View

2.
Bray F, Parkin D . Cancer in sub-Saharan Africa in 2020: a review of current estimates of the national burden, data gaps, and future needs. Lancet Oncol. 2022; 23(6):719-728. DOI: 10.1016/S1470-2045(22)00270-4. View

3.
Liao L, Chen C, Li N, Lin L, Huang B, Chang Y . Y-Box Binding Protein-1 Promotes Epithelial-Mesenchymal Transition in Sorafenib-Resistant Hepatocellular Carcinoma Cells. Int J Mol Sci. 2020; 22(1). PMC: 7795419. DOI: 10.3390/ijms22010224. View

4.
Chen Y, Huang H, Li Y, Xiao W, Liu Y, Chen R . TIGIT Blockade Exerts Synergistic Effects on Microwave Ablation Against Cancer. Front Immunol. 2022; 13:832230. PMC: 8935077. DOI: 10.3389/fimmu.2022.832230. View

5.
CUNNINGHAM K, Manson W, SPRING F, Hutchinson S . Cordycepin, a metabolic product isolated from cultures of Cordyceps militaris (Linn.) Link. Nature. 1950; 166(4231):949. DOI: 10.1038/166949a0. View