Please use this identifier to cite or link to this item: http://umt-ir.umt.edu.my:8080/handle/123456789/5852
Title: Cervicare™ Induces Apoptosis In Hela And Caski Cells Through ROS Production And Loss Of Mitochondrial Membrane Potential
Authors: Neda, Amini
Fadzilah Adibah, Abdul Majid
Mohsen, Marvibaigi
Eko, Supriyanto
Saravana Kumar, Jaganathan
Wong, Tet Soon
Rozita, Nasiri
Javad, Hamzehalipour
Keywords: Anticancer
Issue Date: 22-Feb-2016
Publisher: RSC Advances
Citation: Vol.6 ; 24391-24417 p.
Abstract: Cervicare™ is a poly-herbal preparation comprised of a combination of 6 plants; most have demonstrated antimicrobial and anticancer properties in preclinical studies. The effect of the ethanol and aqueous extracts of Cervicare™ on cell proliferation and apoptosis using cervical cancer HeLa and CaSki cells was investigated for the first time in the present study. MTT assay results showed that Cervicare™ extracts exerted time- and dose-dependent inhibition of cell viability. The hallmark properties of apoptosis like cell shrinkage and cytoplasmic condensation were observed using an inverted phase contrast microscope, ethidium bromide/ acridine orange and Hoechst 33342/propidium iodide fluorescent staining methods. Furthermore, our results demonstrated that Cervicare™ extracts induced apoptosis in HeLa and CaSki cells by ROS generation and mitochondrial depolarization in a concentration dependent manner. The results showed that Cervicare™ extracts were capable of suppressing cell migration and inhibiting colony formation in a dose-dependent manner. Moreover, western blot analysis demonstrated the involvement of a mitochondria-dependent apoptosis pathway in the apoptosis inducing activity of Cervicare™ ethanol extract in HeLa cells. GC-MS analysis of the ethanolic extract afforded the identification of 40 substances, showing that it was primarily composed of anti-cancerous compounds such as xanthorrhizol (60.40%), octacosane (9.93%) and squalene (1.24%). Together, these results point out the Cervicare™ mediated inhibition of HeLa cell growth via induction of apoptosis and that it may be a potential anticancer agent which deserves further investigation.
URI: http://hdl.handle.net/123456789/5852
ISSN: 2046-2069
Appears in Collections:Journal Articles



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