Involvement of Caspase-۳ Pathway in Anti-cancer Properties of Genistein in AGS Gastric Cancer Cell Line is Still Enigmatic
محل انتشار: مجله بیوشیمی پزشکی، دوره: 10، شماره: 1
سال انتشار: 1401
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 150
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شناسه ملی سند علمی:
JR_MEBIO-10-1_002
تاریخ نمایه سازی: 28 تیر 1402
چکیده مقاله:
Background: Genistein is an isoflavone that has been reported to have various anti-cancer properties.
Objectives: This study aimed to reveal whether or not the anti-cancer properties of genistein in AGS gastric
cancer cell line were mediated through caspase-۳ enzyme.
Methods: AGS gastric cancer cells were treated with different concentrations of genistein for ۱۲, ۲۴, and
۴۸ hours and, then, the viability of the cells and IC۵۰ were determined. To determine the effect of genistein
on AGS cell migration potency, the wound healing assay was performed. The genistein-induced apoptosis
in AGS gastric cells was evaluated by flow cytometry. Caspase-۳ gene (CASP۳) expression level and its
enzyme activity level were determined by reverse transcription quantitative polymerase chain reaction
(RT-qPCR) and colorimetric techniques, respectively.
Results: The IC۵۰ value was calculated as ۷۰ μM concentration for ۲۴ hours of incubation with genistein.
Genistein significantly reduced AGS cell migration compared to the untreated control cells (P < ۰.۰۰۱).
Genistein increased the early and late apoptosis of the cells (P < ۰.۰۰۱) and upregulated the caspase-۳ gene
expression (P < ۰.۰۰۱), but did not significantly enhance the caspase-۳ enzyme activity in treated cells.
Conclusion: Genistein exhibited anti-cancer effects on AGS cells to some extent by reducing cellular
migration, increasing apoptosis, and upregulating CASP۳ gene expression; however, it did not alter the
caspse-۳ activity. Therefore, it was recommended that more studies should be carried out to delineate the
role of caspase-۳ in health benefits attributed to the genistein.
کلیدواژه ها:
نویسندگان
Neda Ghasemkhani
Department of Clinical Biochemistry, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran
Gholamreza Shafiee
Department of Clinical Biochemistry, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran
Masoud Saidijam
Department of Molecular Medicine and Human Genetics, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran
Heidar Tayebinia
Department of Clinical Biochemistry, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran