El-Huneidi Waseem, Shehab Naglaa G, Bajbouj Khuloud, Vinod Arya, El-Serafi Ahmed, Shafarin Jasmin, Bou Malhab Lara J, Abdel-Rahman Wael M, Abu-Gharbieh Eman
Department of Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah 27272, UAE.
Department of Pharmaceutical Chemistry and Natural Products, Dubai Pharmacy College, Dubai 19099, UAE.
Pharmaceuticals (Basel). 2020 Jun 3;13(6):115. doi: 10.3390/ph13060115.
() has been used widely in folk medicine to alleviate various ailments such as abdominal pains, diarrhea, colds, eye infections, heart disorders and wounds. A few reports have confirmed different therapeutic potentialities of its extracts, including the anti-inflammatory, gastroprotective, analgesic, antiobesity and antidiabetic activities. This study aimed to investigate the mechanistic pathway of the antiproliferative activity of the ethanolic extract of on two different cancer cell lines, namely human breast (mammary carcinoma F7 (MCF-7)) and human colorectal (human colon tumor cells (HCT-116)) cell lines. The 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide tetrazolium (MTT) assay, Annexin V-FITC/PI, caspases 8/9 and cell cycle analyses, qRT-PCR and Western blot were used to assess the effect of on cytotoxicity, apoptosis, cell cycle, cell cycle-related genes and protein expression profiles in MCF-7 and HCT-116. The extract inhibits cell proliferation in a time- and dose-dependent manner. The half-maximal inhibitory concentration (IC) for both cell lines was found to be 100 μg/mL. Apoptosis induction was confirmed by Annexin V-FITC/PI, that was related to caspases 8 and 9 activities induction. Furthermore, the cell cycle analysis revealed arrest at G2/M phase. The underlying mechanism involved in the G2/M arrest was found to be associated with the downregulation of CDK1, cyclin B1 and survivin that was confirmed by qRT-PCR and Western blotting.
()已在民间医学中广泛用于缓解各种疾病,如腹痛、腹泻、感冒、眼部感染、心脏疾病和伤口。一些报告证实了其提取物具有不同的治疗潜力,包括抗炎、胃保护、镇痛、抗肥胖和抗糖尿病活性。本研究旨在探讨(此处原文缺失具体物质名称)乙醇提取物对两种不同癌细胞系,即人乳腺(乳腺癌F7(MCF-7))和人结肠(人结肠肿瘤细胞(HCT-116))细胞系的抗增殖活性的作用机制。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法、膜联蛋白V-FITC/PI法、半胱天冬酶8/9法和细胞周期分析、qRT-PCR和蛋白质印迹法来评估(此处原文缺失具体物质名称)对MCF-7和HCT-116细胞的细胞毒性、凋亡、细胞周期、细胞周期相关基因和蛋白质表达谱的影响。提取物以时间和剂量依赖性方式抑制细胞增殖。两种细胞系的半数最大抑制浓度(IC)均为100μg/mL。膜联蛋白V-FITC/PI法证实了凋亡诱导,这与半胱天冬酶8和9的活性诱导有关。此外,细胞周期分析显示细胞停滞在G2/M期。发现G2/M期停滞所涉及的潜在机制与细胞周期蛋白依赖性激酶1(CDK1)、细胞周期蛋白B1和生存素的下调有关,qRT-PCR和蛋白质印迹法证实了这一点。