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10.18632/oncotarget.7969

http://scihub22266oqcxt.onion/10.18632/oncotarget.7969
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C5349872!5349872!26967390
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suck abstract from ncbi


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pmid26967390      Oncotarget 2016 ; 7 (52): 85764-75
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  • Granulocyte-like myeloid derived suppressor cells (G-MDSC) are increased in multiple myeloma and are driven by dysfunctional mesenchymal stem cells (MSC) #MMPMID26967390
  • Giallongo C; Tibullo D; Parrinello NL; La Cava P; Di Rosa M; Bramanti V; Di Raimondo C; Conticello C; Chiarenza A; Palumbo GA; Avola R; Romano A; Di Raimondo F
  • Oncotarget 2016[Dec]; 7 (52): 85764-75 PMID26967390show ga
  • Granulocytic-Myeloid-derived suppressor cells (G-MDSC) are increased in Multiple Myeloma (MM) patients but the mechanisms of G-MDSC generation are still unknown. There are many evidences of the role of mesenchymal stem cells (MSC) in promoting MM cell growth, survival and drug-resistance. We here used a specific experimental model in vitro to evaluate the ability of MSC to induce G-MDSC. We found that although MSC derived from healthy donors (HD), MGUS and MM were able to generate the same amount of MDSC, only MM-MSC-educated G-MDSC exhibited suppressive ability. In addition, in comparison with MSC derived from HD, MM-MSC produce higher amount of immune-modulatory factors that could be involved in MDSC induction. Compared to G-MDSC obtained from co-culture models with MSC from healthy subjects, both MGUS and MM-MSC-educated G-MDSC showed increase of immune-modulatory factors. However, only MM-MSC educated G-MDSC 1) up-regulated immune-suppressive factors as ARG1 and TNF?, 2) expressed higher levels of PROK2, important in angiogenesis and inflammatory process, and 3) showed ability to digest bone matrix.Our data demonstrate that MM-MSC are functionally different from healthy subjects and MGUS-MSC, supporting an evolving concept regarding the contribution of MM-MSC to tumor development and progression.
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