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10.2147/OTT.S168317

http://scihub22266oqcxt.onion/10.2147/OTT.S168317
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C6038883!6038883!30013362
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suck abstract from ncbi


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pmid30013362      Onco+Targets+Ther 2018 ; 11 (ä): 3817-26
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  • Tumor-associated macrophage-derived cytokines enhance cancer stem-like characteristics through epithelial?mesenchymal transition #MMPMID30013362
  • Chen Y; Tan W; Wang C
  • Onco Targets Ther 2018[]; 11 (ä): 3817-26 PMID30013362show ga
  • Cancer stem cells are a small population of cells with the potential for self-renewal and multi-directional differentiation and are an important source of cancer initiation, treatment resistance, and recurrence. Epithelial?mesenchymal transition (EMT) is a process in which epithelial cells lose their epithelial phenotype and convert to mesenchymal cells. Recent studies have shown that cancer cells undergoing EMT can become stem-like cells. Many kinds of tumors are associated with chronic inflammation, which plays a role in tumor progression. Among the various immune cells mediating chronic inflammation, macrophages account for ~30%?50% of the tumor mass. Macrophages are highly infiltrative in the tumor microenvironment and secrete a series of inflammatory factors and cytokines, such as transforming growth factor (TGF)-?, IL-6, IL-10, and tumor necrosis factor (TNF)-?, which promote EMT and enhance the stemness of cancer cells. This review summarizes and discusses recent research findings on some specific mechanisms of tumor-associated macrophage-derived cytokines in EMT and cancer stemness transition, which are emerging targets of cancer treatment.
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