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Atractylenolide II Induces G1 Cell-Cycle Arrest and Apoptosis in B16 Melanoma Cells

Yan Ye, Hui Wang, Jian-Hong Chu, Gui-Xin Chou, Si-Bao Chen, Huanbiao Mo, Wang-Fun Fong, Zhi-Ling Yu

J Ethnopharmacol. 2011 Jun 14;136(1):279-82.

PMID: 21524699

Abstract:

Ethnopharmacological relevance:
Atractylenolide II (AT-II) is a sesquiterpene compound isolated from the dried rhizome of Atractylodes macrocephala (Baizhu in Chinese), which is traditionally prescribed for melanoma treatment by Chinese medicine practitioners. Our previous study showed that AT-II can inhibit B16 cells proliferation. Here we investigate the mechanistic basis for the anti-proliferative activity of AT-II in B16 melanoma cells.
Materials and methods:
Cell viability was examined by MTT assay. Cell cycle distribution and apoptosis were determined by flow cytometry. Protein expression was determined by Western blotting.
Results:
AT-II treatment for 48 h dose-dependently inhibited cell proliferation with an IC(50) of 82.3 μM, and induced G1 phase cell cycle arrest. Moreover, treatment with 75 μM AT-II induced apoptosis. These observations were associated with the decrease of the expression of Cdk2, phosphorylated-Akt, phosphorylated-ERK and Bcl-2, the increase of the expression of phosphorylated-p38, phosphorylated-p53, p21, p27, and activation of caspases-8, -9 and -3. In addition, a chemical inhibitor of p53, PFTα, significantly decreased AT-II-mediated growth inhibition and apoptosis.
Conclusions:
We demonstrated that the G1-arresting and apoptotic effects of AT-II in B16 cells involve p38 activation as well as ERK and Akt inactivation, and the cytotoxic/apoptotic effects of AT-II are potentially p53 dependent. These findings provided chemical and pharmacological basis for the traditional application of Baizhu in melanoma treatment.

Chemicals Related in the Paper:

Catalog Number Product Name Structure CAS Number Price
AP73069144 Atractylenolide II Atractylenolide II 73069-14-4 Price
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