Author/Authors :
Karimi, Ali Medical Plants Research Center - Basic Health Sciences Institute - Shahrekord University of Medical Sciences, Shahrekord, Iran , Moradi, Mohammad-taghi Medical Plants Research Center - Basic Health Sciences Institute - Shahrekord University of Medical Sciences, Shahrekord, Iran , lorigooini, Zahra Medical Plants Research Center - Basic Health Sciences Institute - Shahrekord University of Medical Sciences, Shahrekord, Iran , Hashemi, Leila Clinical Biochemistry Research Center - Basic Health Sciences Institute - Shahrekord University of Medical Sciences, Shahrekord, Iran , Alidadi, Somayeh Cellular and Molecular Research Center - Basic Health Sciences Institute - Shahrekord University of Medical Sciences, Shahrekord, Iran , Saeedi, Mojtaba Cellular and Molecular Research Center - Basic Health Sciences Institute - Shahrekord University of Medical Sciences, Shahrekord, Iran
Abstract :
Cancer leads to over seven million deaths each year. The current
therapeutic approaches have failed to completely treat cancer, and it is
essential to seek out new effective anticancer drugs. Because of nontoxic
properties, relatively low cost, and phytochemical compounds, medicinal
plant extracts have been evaluated for anticancer effects. The present
study investigated antiproliferative, apoptosis-inducing, and total phenolic
content of the flower bud extract of dried Syzygium aromaticum L. on
human cervical cancer (HeLa) cells. Ethanolic extract of dried flower buds
was prepared and total phenolic and flavonoid content determined. In
vitro antiproliferative activity of the extract in Hela and normal human
dermal fibroblasts (HDFs) was evaluated using MTT assay. To determine
apoptosis induction, HeLa cells were incubated with one time IC50
concentrations of extract, stained with both annexin V-fluorescein
isothiocyanate and propidium iodide, and flowcytometrically analyzed.
Total phenolic and flavonoid content was 225.6±4 mg GAE/g and
29.3±2.35 mg RUT/g, respectively. Antiproliferative activity results
showed that cell viability significantly decreased in dose- and timedependent
manner after extract treatment (p<0.05). The extract IC50
against HeLa cell was less than that against HDFs. Flow cytometry results
showed that the extract induced Hela cell apoptosis (apoptosis ratio:
66.77%). The ethanolic extract of dried S. aromaticum flower bud had the
greatest phenolic content, and suppressed the proliferation of HeLa cells
probably by inducing apoptosis. Further studies may identify the main
anticancer ingredients of this extract.
Keywords :
Human cervical cancer , Proliferation , Cancer , Syzygium aromaticum L. , Apoptosis