Planta Med 2009; 75(2): 127-131
DOI: 10.1055/s-0028-1088366
Pharmacology
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Anti-Cancer Effect of Betulin on a Human Lung Cancer Cell Line: A Pharmacoproteomic Approach Using 2 D SDS PAGE Coupled with Nano-HPLC Tandem Mass Spectrometry

Jae Sung Pyo1 , Si Hun Roh1 , Dae Ki Kim1 , Jin Gyun Lee1 , Yong Yook Lee1 , Soon Sun Hong2 , Sung Won Kwon1 , Jeong Hill Park1
  • 1College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Korea
  • 2College of Medicine (BK21), Inha University, Incheon, Korea
Further Information

Publication History

Received: August 22, 2008 Revised: September 25, 2008

Accepted: October 2, 2008

Publication Date:
12 December 2008 (online)

Abstract

Betulin is a representative compound of Betula platyphylla, a tree species belonging to the Betulaceae family. In this investigation, we revealed that betulin showed anticancer activity on human lung cancer A549 cells by inducing apoptosis and changes in protein expression profiles were observed. Upon flow cytometry analysis, the surface of betulin-treated cells was found to be annexin-V positive and propidium iodide (PI) negative, which indicated that the cells were apoptotic. In order to identify the molecular players involved in betulin-induced apoptosis, cellular proteins were applied to two-dimensional sodium dodecyl sulfate polyacrylamide gel electrophoresis (2 D SDS PAGE) for differential proteomic analysis. As a result, four downregulated proteins and three upregulated proteins were identified by nano-HPLC MS/MS. The four downregulated proteins were poly(rC)-binding protein 1, isoform 1 of 3-hydroxyacyl-CoA dehydrogenase type 2, heat shock protein 90-alpha 2, and enoyl-CoA hydratase; the three upregulated proteins were aconitate hydratase, malate dehydrogenase, and splicing factor arginine/serine-rich 1. These differentially expressed proteins explained the cytotoxicity of betulin against human lung cancer A549 cells, and the proteomic approach was thus shown to be a potential tool for understanding the pharmacological activities of pharmacophores.

Abbreviations

ACN:acetonitrile

DMSO:dimethyl sulfoxide

FACS:fluorescence activated cell sorter

HEPES:4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid

MTT:methylthiazolelyldiphenyl-tetrazolium bromide

PI:prodidium iodide

TFA:trifluoroacetic acid

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Prof. Jeong Hill Park

College of Pharmacy

Seoul National University

Seoul 151–742

Korea

Phone: +82-2-880-7857

Fax: +82-2-887-7857

Email: hillpark@snu.ac.kr

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