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Caffeine induces sustained apoptosis of human gastric cancer cells by activating the caspase-9/caspase-3 signalling pathway

机译:咖啡因通过激活caspase-9 / caspase-3信号通路诱导人胃癌细胞持续凋亡

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摘要

Caffeine is one of the most widely consumed substances found in beverages, and has demonstrated anticancer effects in several types of cancer. The present study aimed to examine the anticancer effects of caffeine on gastric cancer (GC) cells (MGC-803 and SGC-7901) in vitro, and to determine whether the apoptosis-related caspase-9/−3 pathway is associated with these effects. The sustained antiproliferative effects of caffeine on gastric cancer were also investigated. GC cell viability and proliferation were evaluated using cell counting and colony forming assays, following treatment with various concentrations of caffeine. Flow cytometry was performed to assess cell cycle dynamics and apoptosis. Western blot analysis was conducted to detect the activity of the caspase-9/−3 pathway. The results indicated that caffeine treatment significantly suppressed GC cell growth and viability and induced apoptosis by activating the caspase-9/−3 pathway. Furthermore, the anticancer effects of caffeine appeared to be sustained, as the caspase-9/−3 pathway remained active following caffeine withdrawal. In conclusion, caffeine may function as a sustained anticancer agent by activating the caspase-9/−3 pathway, which indicates that it may be useful as a therapeutic candidate in gastric cancer.
机译:咖啡因是饮料中消耗最广泛的物质之一,并且已在多种癌症中显示出抗癌作用。本研究旨在探讨咖啡因在体外对胃癌细胞(MGC-803和SGC-7901)的抗癌作用,并确定凋亡相关的caspase-9 / -3途径是否与这些作用有关。还研究了咖啡因对胃癌的持续抗增殖作用。在用各种浓度的咖啡因处理后,使用细胞计数和集落形成测定法评估GC细胞的活力和增殖。进行流式细胞术以评估细胞周期动态和凋亡。进行蛋白质印迹分析以检测caspase-9 / -3途径的活性。结果表明,咖啡因处理可通过激活caspase-9 / -3途径显着抑制GC细胞的生长和活力,并诱导细胞凋亡。此外,咖啡因的抗癌作用似乎得以持续,因为戒断咖啡因后caspase-9 / -3途径仍然活跃。总而言之,咖啡因可以通过激活caspase-9 / -3途径作为持续的抗癌药,这表明它可以用作胃癌的治疗候选药物。

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