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Molecules 2011, 16, 2944-2959; doi:10.3390/moleculeOPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Article
Selective Cytotoxicity of Goniothalamin against Hepatoblastoma
HepG2 Cells
Mothanna Al-Qubaisi 1, Rosli Rozita 2, Swee-Keong Yeap 1, Abdul-Rahman Omar 3,
Abdul-Manaf Ali 4 and Noorjahan B. Alitheen 1,*
1
Department of Cell and Molecular Biology, Faculty of Biotechnology and Biomolecular Sciences,
University Putra Malaysia (UPM), 43400, Serdang, Selangor, Malaysia
2
Department of Obstetric and Gynaecology, Faculty of Medicine and Health Sciences, University
Putra Malaysia (UPM), 43400, Serdang, Selangor, Malaysia
3
Department of Veterinary Pathology and Microbiology, Faculty of Veterinary Medicine, University
Putra Malaysia (UPM), 43400, Serdang, Selangor, Malaysia
4
Faculty of Agriculture and Biotechnology, University Sultan Zainal Abidin (UniSZA), Kampus
Kota, Jalan Sultan Mahmud, 20400 Kuala Terengganu, Malaysia
* Author to whom correspondence should be addressed; E-Mails: noorjahan@.my or
noorjahan@; Tel.: +603-8946 7471; Fax: +603-8946 7510.
Received: 17 January 2011; in revised form: 11 March 2011 / Accepted: 17 March 2011 /
Published: 6 April 2011
Abstract: Liver cancer has become one of the major types of cancer with high mortality
and liver cancer is not responsive to the current cytotoxic agents used in chemotherapy.
The purpose of this study was to examine the in vitro cytotoxicity of goniothalamin on
human hepatoblastoma HepG2 cells and normal liver Chang cells. The cytotoxicity of
goniothalamin against HepG2 and liver Chang cell was tested using MTT cell viability
assay, LDH leakage assay, cell cycle flow cytometry PI analysis, BrdU proliferation
ELISA assay and trypan blue dye exclusion assay. Goniothalamin selectively inhibited
HepG2 cells [IC50 = 4.6 (±0.23) μM in the MTT assay; IC50 = 5.20 (±0.01) μM for LDH
assay at 72 hours], with less sensitivity in Cha
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