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Apicularen A acetate induces cell death via AIF translocation and disrupts the microtubule network by down-regulating tubulin in HM7 human colon cancer cells.
Seo, Kang-Sik; Kim, Hoon; Hong, Tae-Hwa; Kim, Jong-Seok; Song, Kyoung-Sub; Yun, Eun-Jin; Park, Ji-Hoon; Jung, Young-Hoon; Park, Jong-Il; Kweon, Gi Ryang; Yoon, Wan-Hee; Lim, Kyu; Hwang, Byung-Doo.
Affiliation
  • Seo KS; Department of Biochemistry, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Biochem Biophys Res Commun ; 434(3): 634-40, 2013 May 10.
Article in En | MEDLINE | ID: mdl-23583412
Apicularen A is a novel antitumor agent and strongly induces death in tumor cells. In this study, we synthesized apicularen A acetate, an acetyl derivative of apicularen A, and investigated its antitumor effect and mechanism in HM7 colon cancer cells. Apicularen A acetate induced apoptotic cell death and caspase-3 activation; however, the pan-caspase inhibitor Z-VAD-fmk could not prevent this cell death. Apicularen A acetate induced the loss of mitochondrial membrane potential and the translocation of apoptosis-inducing factor (AIF) from mitochondria. In addition, apicularen A acetate significantly decreased tubulin mRNA and protein levels and induced disruption of microtubule networks. Taken together, these results indicate that the mechanism of apicularen A acetate involves caspase-independent apoptotic cell death and disruption of microtubule architecture.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tubulin / Down-Regulation / Apoptosis / Colonic Neoplasms / Bridged Bicyclo Compounds, Heterocyclic / Apoptosis Inducing Factor / Microtubules Limits: Humans Language: En Journal: Biochem Biophys Res Commun Year: 2013 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tubulin / Down-Regulation / Apoptosis / Colonic Neoplasms / Bridged Bicyclo Compounds, Heterocyclic / Apoptosis Inducing Factor / Microtubules Limits: Humans Language: En Journal: Biochem Biophys Res Commun Year: 2013 Type: Article