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Various bone marrow niches, cell types, and cues that regulate the dormancy of disseminated tumor cells and hematopoietic stem cells

Various bone marrow niches, cell types, and cues that regulate the dormancy of disseminated tumor cells and hematopoietic stem cells
The various BM niches, cell types and cues that regulate the dormancy of DTCs and HSCs. Both the osteoblastic niche and the perivascular niche in the BM are involved in DTC dormancy by producing a wide range of cues (cytokines, microRNA, extracellular vesicles, cell–cell contact signaling, etc.) that drive dormancy. Additionally, dormant cancer cells downregulate antigen presentation and upregulate immunosuppressive ligands in order to evade recognition by the immune system. Over time and reciprocally, cancer cells also remodel their surrounding microenvironment and hypothetically feed a proliferative positive loop.
HSC: hematopoietic stem cell; EVs: extracellular vesicles; ECs: endothelial cells; PD-1: programmed cell death protein 1; PD-L1: programmed cell death ligand 1; CTLA-4: cytotoxic T-lymphocyte antigen-4; miR: microRNA; MHC: major histocompatibility complex; MHCI: MHC class I; vWF: von Willebrand factor; MSC: mesenchymal stem cell; BM: bone marrow; DTC: disseminated tumor cells.
Reprinted by permission from Macmillan Publishers Ltd: Nature Cancer. Risson E, Nobre AR, Maguer-Satta V, Aguirre-Ghiso JA. The current paradigm and challenges ahead for the dormancy of disseminated tumor cells. Nat Cancer 2020; 1:672. Copyright © 2020. https://www.nature.com/natcancer/.
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