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Minnelide: a novel therapeutic that promotes apoptosis in non-small cell lung carcinoma in vivo.


ABSTRACT: BACKGROUND:Minnelide, a pro-drug of triptolide, has recently emerged as a potent anticancer agent. The precise mechanisms of its cytotoxic effects remain unclear. METHODS:Cell viability was studied using CCK8 assay. Cell proliferation was measured real-time on cultured cells using Electric Cell Substrate Impedence Sensing (ECIS). Apoptosis was assayed by Caspase activity on cultured lung cancer cells and TUNEL staining on tissue sections. Expression of pro-survival and anti-apoptotic genes (HSP70, BIRC5, BIRC4, BIRC2, UACA, APAF-1) was estimated by qRTPCR. Effect of Minnelide on proliferative cells in the tissue was estimated by Ki-67 staining of animal tissue sections. RESULTS:In this study, we investigated in vitro and in vivo antitumor effects of triptolide/Minnelide in non-small cell lung carcinoma (NSCLC). Triptolide/Minnelide exhibited anti-proliferative effects and induced apoptosis in NSCLC cell lines and NSCLC mouse models. Triptolide/Minnelide significantly down-regulated the expression of pro-survival and anti-apoptotic genes (HSP70, BIRC5, BIRC4, BIRC2, UACA) and up-regulated pro-apoptotic APAF-1 gene, in part, via attenuating the NF-?B signaling activity. CONCLUSION:In conclusion, our results provide supporting mechanistic evidence for Minnelide as a potential in NSCLC.

SUBMITTER: Rousalova I 

PROVIDER: S-EPMC3797124 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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Minnelide: a novel therapeutic that promotes apoptosis in non-small cell lung carcinoma in vivo.

Rousalova Ilona I   Banerjee Sulagna S   Sangwan Veena V   Evenson Kristen K   McCauley Joel A JA   Kratzke Robert R   Vickers Selwyn M SM   Saluja Ashok A   D'Cunha Jonathan J  

PloS one 20131015 10


<h4>Background</h4>Minnelide, a pro-drug of triptolide, has recently emerged as a potent anticancer agent. The precise mechanisms of its cytotoxic effects remain unclear.<h4>Methods</h4>Cell viability was studied using CCK8 assay. Cell proliferation was measured real-time on cultured cells using Electric Cell Substrate Impedence Sensing (ECIS). Apoptosis was assayed by Caspase activity on cultured lung cancer cells and TUNEL staining on tissue sections. Expression of pro-survival and anti-apopto  ...[more]

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