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10.3892/ol.2017.6669

http://scihub22266oqcxt.onion/10.3892/ol.2017.6669
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C5604146!5604146!28943944
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suck abstract from ncbi


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pmid28943944      Oncol+Lett 2017 ; 14 (4): 4305-10
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  • Andrographolide suppresses proliferation of human colon cancer SW620 cells through the TLR4/NF-?B/MMP-9 signaling pathway #MMPMID28943944
  • Zhang R; Zhao J; Xu J; Jiao DX; Wang J; Gong ZQ; Jia JH
  • Oncol Lett 2017[Oct]; 14 (4): 4305-10 PMID28943944show ga
  • Modern pharmacological research has revealed that andrographolide has various functions, including anti-bacterial, anti-inflammatory and anti-viral effects, immunoregulation, treating cardiovascular and cerebrovascular diseases, and prevention and treatment of alcoholic liver injury. The present study investigated whether andrographolide suppresses the proliferation of human colon cancer cell through the Toll-like receptor 4 (TLR4)/nuclear factor (NF)-?B/matrix metalloproteinase-9 (MMP-9) signaling pathway. The MTT assay and lactate dehydrogenase assay were used to evaluate the anticancer effects of andrographolide on cell proliferation and cytotoxicity in human colon cancer SW620 cells. Flow cytometry was used to analyze the anticancer effects of andrographolide on apoptosis by Annexin V-fluorescein isothiocyanate/propidium iodide kit. The effects of andrographolide on the activity of caspase-3/9 were measured using ELISA. Western blot analysis was also used to analyze the protein expression of TLR4, myeloid differentiation primary response gene 88 (MyD88), NF-?B-p65 and MMP-9. In the present study, it was found that andrographolide suppressed the cell proliferation, augmented cytotoxicity, evoked cell apoptosis and activated caspase-3/9 activities in human colon cancer SW620 cells. The results revealed that the anti-proliferation effects of andrographolide on the SW620 cells was associated with the inhibition of TLR4, MyD88, NF-?B-p65 and MMP-9 signaling activation. The results suggest that andrographolide is a promising drug for treatment of human colon cancer via suppression of the TLR4/NF-?B/MMP-9 signaling pathway.
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