DocumentCode
2525209
Title
The Proliferative Inhibition and Apoptotic Mechanism of Saikosaponin D in Human Non-Small Cell Lung Cancer A549 Cells
Author
Jiang Dong ; Yang Ru-song ; Zheng Shi-ying ; Ge Jin-feng ; Zhao Jun
Author_Institution
Dept. of Thoracocardiac Surg., First Affiliated Hosp. of Suzhou Univ., Suzhou, China
fYear
2009
fDate
11-13 June 2009
Firstpage
1
Lastpage
10
Abstract
Saikosaponin D is a saponin extract derived from several species of Bupleurum (Umbelliferae), which is used for the treatment of various liver diseases in traditional Chinese medicine. In this study, we report that Saikosaponin D inhibits the cell growth of human lung cancer cell line A549 and provide a molecular understanding of this effect. The results showed that Saikosaponin D inhibited the proliferation of A549 by inducing apoptosis and blocking cell cycle progression in the G1 phase. ELISA assay showed that Saikosaponin D significantly increased the expression of p53 and p21/WAFl protein, contributing to cell cycle arrest. An enhancement in Fas/APO-1 and its two form ligands, membrane-bound Fas ligand (mFasL) and soluble Fas ligand (sFasL), as well as Bax protein, was responsible for the apoptotic effect induced by Saikosaponin D. Taken together, our study suggests that the induction of p53 and activity of the Fas/FasL apoptotic system may participate in the antiproliferative activity of Saikosaponin D in A549 cells.
Keywords
biomembranes; cancer; cellular biophysics; drugs; lung; patient treatment; proteins; tumours; Bupleurum species; Fas-FasL apoptotic system; Saikosaponin D apoptotic mechanism; blocking cell cycle progression; cell growth; cell proliferation; membrane-bound Fas ligand; p21-WAFl protein; small cell lung cancer A549 cell; Birth disorders; Cancer; Cells (biology); Hospitals; Humans; Immune system; Lungs; Medical treatment; Oncological surgery; Testing;
fLanguage
English
Publisher
ieee
Conference_Titel
Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
Conference_Location
Beijing
Print_ISBN
978-1-4244-2901-1
Electronic_ISBN
978-1-4244-2902-8
Type
conf
DOI
10.1109/ICBBE.2009.5163644
Filename
5163644
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