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10.1038/srep36663

http://scihub22266oqcxt.onion/10.1038/srep36663
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C5114612!5114612 !27857157
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suck abstract from ncbi


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pmid27857157
      Sci+Rep 2016 ; 6 (ä): 36663
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  • Inhibiting MDSC differentiation from bone marrow with phytochemical polyacetylenes drastically impairs tumor metastasis #MMPMID27857157
  • Wei WC ; Lin SY ; Lan CW ; Huang YC ; Lin CY ; Hsiao PW ; Chen YR ; Yang WC ; Yang NS
  • Sci Rep 2016[Nov]; 6 (ä): 36663 PMID27857157 show ga
  • Myeloid-derived suppressor cells (MDSCs) are implicated in the promotion of tumor metastasis by protecting metastatic cancerous cells from immune surveillance and have thus been suggested as novel targets for cancer therapy. We demonstrate here that oral feeding with polyacetylenic glycosides (BP-E-F1) from the medicinal plant Bidens pilosa effectively suppresses tumor metastasis and inhibits tumor-induced accumulation of granulocytic (g) MDSCs, but does not result in body weight loss in a mouse mammary tumor-resection model. BP-E-F1 is further demonstrated to exert its anti-metastasis activity through inhibiting the differentiation and function of gMDSCs. Pharmacokinetic and mechanistic studies reveal that BP-E-F1 suppresses the differentiation of gMDSCs via the inhibition of a tumor-derived, G-CSF-induced signaling pathway in bone marrow cells of test mice. Taken together, our findings suggest that specific plant polyacetylenic glycosides that target gMDSC differentiation by communicating with bone marrow cells may hence be seriously considered for potential application as botanical drugs against metastatic cancers.
  • |Animals [MESH]
  • |Bidens/chemistry [MESH]
  • |Cell Differentiation [MESH]
  • |Cell Line, Tumor [MESH]
  • |Granulocyte Colony-Stimulating Factor/metabolism [MESH]
  • |Heterografts [MESH]
  • |Humans [MESH]
  • |Mice [MESH]
  • |Mice, Transgenic [MESH]
  • |Myeloid-Derived Suppressor Cells/cytology/*drug effects [MESH]
  • |Neoplasm Metastasis/*prevention & control [MESH]
  • |Phytochemicals/*pharmacology [MESH]


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