Antitumor Activity of β-glucan Isolated from Phoenix Dactylifera L. Fruits on Cancer and Normal Cell Lines
سال انتشار: 1404
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 103
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شناسه ملی سند علمی:
JR_JOGCR-10-5_010
تاریخ نمایه سازی: 26 اسفند 1403
چکیده مقاله:
Background & Objective: Recent research has focused on β-glucan from Phoenix dactylifera L. fruits as a potential anti-tumor agent. This study investigates its cytotoxic effects on cancer and normal cell lines, exploring its ability to inhibit tumor cell proliferation and activate immune responses, thus evaluating its potential as a selective anticancer treatment.Materials & Methods: β-glucan was extracted from Phoenix dactylifera fruits using hot water extraction (glucan-P۱), ion exchange chromatography (glucan-P۲), and gel filtration chromatography (glucan-P۳). Concentrations ranging from ۳۱.۲۵ to ۱۰۰۰ µg/mL were prepared. MCF-۷, AMJ۱۳, and REF cell lines were cultured in RPMI-۱۶۴۰ medium. Cytotoxicity was assessed using the MTT assay, measuring absorbance at ۵۴۰ nm. Inhibition rates were calculated, and statistical analysis was performed using ANOVA and Dunn's test.Results: The study evaluated the cytotoxic effects of three β-glucan preparations (glucan-P۱, glucan-P۲, and glucan-P۳) on breast cancer cell lines MCF-۷ and AMJ۱۳, as well as normal REF cells. Glucan-P۳ demonstrated the highest growth inhibition across all-time points (۲۴, ۴۸, and ۷۲ hours) for both cancer cell lines. The most significant effect was observed on MCF-۷ cells after ۴۸ hours of exposure, with glucan-P۳ at the highest concentration (۱۰۰۰ µg/ml) achieving ۸۷.۷۷۴% growth inhibition. AMJ۱۳ cells showed similar trends, with glucan-P۳ exhibiting the strongest inhibitory effect. Importantly, all β-glucan preparations showed minimal cytotoxicity towards normal REF cells after ۷۲ hours of exposure, suggesting a selective anti-cancer effect.Conclusion: β-glucan from Phoenix dactylifera showed significant antitumor activity against breast cancer cells with no effect on normal cells, highlighting its therapeutic potential.
کلیدواژه ها:
نویسندگان
Hiba Muhammed Al-Khuzaay
Department of Biology, College of Science, Mustansiriyah University, Baghdad, Iraq
Yasir Hussein Al-Juraisy
Department of Biology, College of Science, Mustansiriyah University, Baghdad, Iraq
Yousif Hussein Mohammed
Department of Mathematics, College of Basic Education, Mustansiriyah University, Baghdad, Iraq
Ali Hussein Alwan
Iraqi Center for Cancer and Medical Genetics Research, Mustansiriyah University, Baghdad, Iraq
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