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Marchantin C, a macrocyclic bisbibenzyl, induces apoptosis of human glioma A172 cells.

Abstract
Macrocyclic bisbibenzyls, a class of characteristic components derived from liverworts, are attracting more and more attention because of their wide range of biological significance, including anti-bacterial, anti-fungus, anti-oxidation and cytotoxicity. Herein, we investigated the pro-apoptotic effect of marchantin C on human glioma A 172 cells. The results demonstrated that marchantin C conferred dose-dependent inhibitory effects onto cell growth, viability and colony formation ability of A 172 cells. Morphological observation and DNA laddering assay showed that marchantin C-treated A172 cells displayed outstanding apoptosis characteristics, such as nuclear fragmentation, the appearance of membrane-enclosed apoptotic bodies and DNA laddering fragment. Moreover, flow cytometric detection of phosphatidylserine externalization indicated that marchantin C-induced apoptosis occurred in a dose-dependent manner. RT-PCR and western blot assay further substantiated that marchantin C, as a promising pro-apoptotic agent, had strong effects to induce A172 cell apoptosis, suggesting that the action was achieved through up-regulating Bax and down-regulating Bcl-2.
AuthorsYan-Qiu Shi, Yong-Xiang Liao, Xian-Jun Qu, Hui-Qing Yuan, Song Li, Jian-Bo Qu, Hong-Xiang Lou
JournalCancer letters (Cancer Lett) Vol. 262 Issue 2 Pg. 173-82 (Apr 18 2008) ISSN: 0304-3835 [Print] Ireland
PMID18215458 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Bibenzyls
  • Catechols
  • Ethers, Cyclic
  • Phenyl Ethers
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • marchantin C
Topics
  • Apoptosis (drug effects)
  • Bibenzyls (pharmacology, therapeutic use)
  • Catechols (pharmacology, therapeutic use)
  • Cell Line, Tumor
  • Cell Proliferation (drug effects)
  • Ethers, Cyclic (pharmacology, therapeutic use)
  • Glioma (drug therapy)
  • Humans
  • Phenyl Ethers (pharmacology, therapeutic use)
  • Proto-Oncogene Proteins c-bcl-2 (metabolism)
  • bcl-2-Associated X Protein (metabolism)

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