Ficus carica叶提取物对B16F10黑色素瘤癌症细胞作用的评价:p53、Caspase-3和Caspase-9在诱导内源性细胞凋亡级联中的作用

IF 1 Q4 PHARMACOLOGY & PHARMACY Jundishapur Journal of Natural Pharmaceutical Products Pub Date : 2021-10-17 DOI:10.5812/jjnpp.117429
Mona Sadeghizade, J. Baharara, Farzaneh Salek, E. Amini
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摘要

背景:黑色素瘤是近几十年来发病率显著增加的最严重的一种皮肤癌,其初级治疗的重要性日益增加。榕叶具有抗炎、抗增殖、抗凋亡等多种治疗作用。目的:因此,本研究针对桑菖蒲对多种疾病的治疗作用,研究桑菖蒲叶甲醇提取物对B16F10黑色素瘤癌细胞诱导凋亡的影响。方法:采用MTT法测定不同浓度的金针叶提取物(150、250、350、450、550、650、750和850 μg /mL)作用于B16F10细胞24和48 h后的细胞存活率,采用AO/PI和DAPI染色、Annexin V/碘化丙啶流式细胞术检测细胞凋亡情况。采用Real-time PCR检测凋亡基因p53、Bax、caspase-3、caspase-9的表达情况。结果:MTT实验结果表明,金针叶甲醇提取物对B16F10细胞的增殖具有剂量和时间依赖性。AO/PI染色结果显示各处理组凋亡细胞数量增加,DAPI结果显示木香提取物导致染色质凝集和断裂。膜联蛋白V显示处理后凋亡细胞百分比增加。此外,凋亡基因的上调通过Real-time PCR证实了carica叶片在B16F10细胞中诱导凋亡的潜力。结论:槐叶醇提物可作为一种有效的抗癌药物,为进一步研究槐叶醇提物对黑色素瘤的作用打下基础。
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Assessment the Effect of Ficus carica Leaf Extract on B16F10 Melanoma Cancer Cells: The Roles of p53, Caspase-3 & Caspase-9 on Induction of Intrinsic Apoptosis Cascade
Background: Melanoma is the most serious kind of skin cancer which has significantly increased in recent decades, and the importance of its primary treatment is increased widely. Ficus carica leaves have various therapeutic impact such as anti-inflammatory, anti-proliferative and apoptotic activity. Objectives: Hence, regarding the F. carica effect on the treatment of various diseases, the present research was conducted to identify the effect of methanolic extract of F. carica leaf on apoptosis induction in B16F10 melanoma cancer cells. Methods: Cell survival was estimated by MTT assay after treatment of B16F10 cells in various concentrations of F. carica leaf extract (150, 250, 350, 450, 550, 650, 750 and 850 μg /mL) for 24 and 48 h. Cell apoptosis was analysed by AO/PI and DAPI staining, Annexin V/Propidium Iodide flow cytometry. Moreover, Real-time PCR was utilized to evaluate the expression of apoptotic genes including p53, Bax, caspase-3 and caspase-9 genes. Results: MTT assay results indicated that methanolic extract of F. carica leaf prevented the proliferation of B16F10 cells in a dose and time dependent manner. AO/PI staining results showed an elevation in apoptotic cells in treated groups and DAPI indicated that F. carica extract resulted in chromatin condensation and fragmentation. Annexin V revealed the increasing percentage of apoptotic cells after treatment. In addition, the up-regulation of apoptotic genes confirmed the apoptosis inducing potential of F. carica leaves in B16F10 cells by Real-time PCR. Conclusions: Thus, methanolic extract of F. carica leaves could be suggested as an effective anti-cancer agent for further studies on melanoma cancer.
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