Drug Res (Stuttg) 2016; 66(10): 532-538
DOI: 10.1055/s-0042-111200
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

In Silico and In Vitro Evaluation of Cytotoxic Activities of Farnesiferol C and Microlobin on MCF-7, HeLa and KYSE Cell Lines

L. Aldaghi
1   Cellular and Molecular Research Center, Sabzevar University of Medical Sciences, Sabzevar, Iran
,
A. Rad
1   Cellular and Molecular Research Center, Sabzevar University of Medical Sciences, Sabzevar, Iran
,
A. Arab
2   Biotechnology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
,
J. Kasaian
3   Natural Products and Medicinal Plants Research Center, North Khorasan University of Medical Sciences, Bojnurd, Iran
,
M. Iranshahi
2   Biotechnology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
,
A. S. Sadr
4   Bioinformatics Research Center, Sabzevar University of Medical Sciences, Sabzevar, Iran
5   Bioinformatics Research Center, Cheragh Medical institute & Hospital, Kabul, Afghanistan
,
F. Soltani
2   Biotechnology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
1   Cellular and Molecular Research Center, Sabzevar University of Medical Sciences, Sabzevar, Iran
› Author Affiliations
Further Information

Publication History

received 06 April 2016

accepted 24 June 2016

Publication Date:
27 July 2016 (online)

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Abstract

Background: Cancer is one of the leading causes of death worldwide. Despite certain advances in cancer therapy, still there is considerable demand for developing efficient therapeutic agents. Nowadays, there is a rising interest in the use of natural-based anti-cancer drugs. In this study, the cytotoxicity of farnesiferol C and microlobin isolated from Ferula szowitsiana was investigated against MCF-7, HeLa and KYSE cancer cell lines. In addition, the mechanism of binding of these compounds to apoptotic proteins (Bax, Bak and Bcl-2) was analyzed by an in silico method.

Materials and methods: We used MTT assay in order to assess the cytotoxicity of compounds against cancer cell lines. For in silico study, the AutoDock 4 was adopted.

Results and discussion: According to the in vitro findings, in general, farnesiferol C showed significant cytotoxicity at higher concentrations (>50 µM) following 48 and 72 h incubation with the selected cancer cells; however, microlobin exhibited almost no activity at concentrations up to 100 µM. The in silico results revealed that both compounds could bind to Bax more efficiently rather than to Bcl-2 or Bak proteins.

Conclusion: The results obtained by our preliminary in vitro and in silico studies suggest that these compounds might induce apoptosis through Bax activation; however further studies, either in vitro or in vivo are needed to clarify these activities.