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MicroRNA-744 promotes cell apoptosis via targeting B cell lymphoma-2 in gastric cancer cell line SGC-7901

机译:MicroRNA-744通过靶向B细胞淋巴瘤2促进胃癌细胞SGC-7901的细胞凋亡

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摘要

Gastric cancer (GC) affects the health of 1,000,000 people per year worldwide; however, the biological basis of GC remains largely unknown. The current study aimed to investigate the aberrant expression of miR-744 in GC for the effective treatment of patients with GC. Tumor and adjacent tissues were obtained from 30 patients who underwent tumor resection surgery at Dongying People's Hospital. The results of reverse transcription-quantitative polymerase chain reaction indicated that the expression of miR-744 was significantly decreased in tumor tissues compared with the levels in adjacent tissues. Human gastric cancer cell line SGC-7901 was then randomly divided into three different groups, including the control, miR-negative control (NC) and miR-744 mimic groups. A Cell Counting Kit-8 assay demonstrated that there was a significant decrease in the proliferation rate of SGC-7901 cells in the miR-744 mimics group compared with that observed in the control and miR-NC mimics groups. In addition, flow cytometry demonstrated that apoptosis was significantly increased in the miR-744 mimics group compared with that observed in the control and miR-NC mimics groups. Western blotting indicated that the expression of B cell lymphoma 2 (Bcl-2), B cell lymphoma-2-associated X protein and caspase-3 protein was significantly increased, while the expression of Bcl-2 was significantly decreased in the miR-744 mimics group compared with the levels observed in the control and miR-NC mimics groups. A dual-luciferase assay verified that miR-744 directly targeted the 3′-untranslated region of Bcl-2. Taken together, the present study suggested that miR-744 serves a tumor suppressive role in GC by targeting Bcl-2.
机译:胃癌(GC)每年影响全世界1,000,000人的健康;但是,GC的生物学基础仍然未知。本研究旨在研究miR-744在GC中的异常表达,以有效治疗GC患者。肿瘤和邻近组织取自东营市人民医院接受肿瘤切除手术的30例患者。逆转录-定量聚合酶链反应的结果表明,与邻近组织相比,miR-744在肿瘤组织中的表达明显降低。然后将人胃癌细胞系SGC-7901随机分为三个不同的组,包括对照组,miR阴性对照组(NC)和miR-744模拟组。 Cell Counting Kit-8分析表明,与对照组和miR-NC模拟组相比,miR-744模拟组中SGC-7901细胞的增殖速率显着降低。另外,流式细胞术表明与对照组和miR-NC模拟物组相比,miR-744模拟物组的凋亡显着增加。 Western blotting结果显示miR-744中B细胞淋巴瘤2(Bcl-2),B细胞淋巴瘤2相关X蛋白和caspase-3蛋白表达明显升高,而Bcl-2表达显着降低。与对照组和miR-NC模拟组中观察到的水平进行比较。双重荧光素酶测定法证实miR-744直接靶向Bcl-2的3'-非翻译区。两者合计,本研究表明miR-744通过靶向Bcl-2在GC中发挥肿瘤抑制作用。

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