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The Role of Erythrocytes and Erythroid Progenitor Cells in Tumors

Overview
Journal Open Life Sci
Specialty Biology
Date 2022 Dec 26
PMID 36567722
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Abstract

In the current research context of precision treatment of malignant tumors, the advantages of immunotherapy are unmatched by conventional antitumor therapy, which can prolong progression-free survival and overall survival. The search for new targets and novel combination therapies can improve the efficacy of immunotherapy and reduce adverse effects. Since current research targets for immunotherapy mainly focus on lymphocytes, little research has been done on erythrocytes. Nucleated erythroid precursor stem cells have been discovered to play an essential role in tumor progression. Researchers are exploring new targets and therapeutic approaches for immunotherapy from the perspective of erythroid progenitor cells (EPCs). Recent studies have shown that different subtypes of EPCs have specific surface markers and distinct biological roles in tumor immunity. CD45 EPCs are potent myeloid-derived suppressor cell-like immunosuppressants that reduce the patient's antitumor immune response. CD45 EPCs promote tumor invasion and metastasis by secreting artemin. A specific type of EPC also promotes angiogenesis and provides radiation protection. Therefore, EPCs may be involved in tumor growth, infiltration, and metastasis. It may also be an important cause of anti-angiogenesis and immunotherapy resistance. This review summarizes recent research advances in erythropoiesis, EPC features, and their impacts and processes on tumors.

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References
1.
Liu D, Niu Z . The structure, genetic polymorphisms, expression and biological functions of complement receptor type 1 (CR1/CD35). Immunopharmacol Immunotoxicol. 2009; 31(4):524-35. DOI: 10.3109/08923970902845768. View

2.
Libregts S, Gutierrez L, de Bruin A, Wensveen F, Papadopoulos P, van IJcken W . Chronic IFN-γ production in mice induces anemia by reducing erythrocyte life span and inhibiting erythropoiesis through an IRF-1/PU.1 axis. Blood. 2011; 118(9):2578-88. DOI: 10.1182/blood-2010-10-315218. View

3.
Elliott S, Pham E, Macdougall I . Erythropoietins: a common mechanism of action. Exp Hematol. 2008; 36(12):1573-84. DOI: 10.1016/j.exphem.2008.08.003. View

4.
Gnanapragasam M, McGrath K, Catherman S, Xue L, Palis J, Bieker J . EKLF/KLF1-regulated cell cycle exit is essential for erythroblast enucleation. Blood. 2016; 128(12):1631-41. PMC: 5034741. DOI: 10.1182/blood-2016-03-706671. View

5.
David C, Massague J . Contextual determinants of TGFβ action in development, immunity and cancer. Nat Rev Mol Cell Biol. 2018; 19(7):419-435. PMC: 7457231. DOI: 10.1038/s41580-018-0007-0. View