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首页> 外文期刊>The Korean Journal of Physiology & Pharmacology >MDL-12330A potentiates TRAIL-induced apoptosis in gastric cancer cells through CHOP-mediated DR5 upregulation
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MDL-12330A potentiates TRAIL-induced apoptosis in gastric cancer cells through CHOP-mediated DR5 upregulation

机译:MDL-12330A通过CHOP介导的DR5上调增强TRAIL诱导的胃癌细胞凋亡

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摘要

MDL-12330A is a widely used adenylyl cyclase (AC) inhibitor that blocks AC/cAMP signaling. In this study, we demonstrated a novel antitumor activity of this drug in gastric carcinoma (GC) cell lines. In these GC cells, MDL-12330A reduced cell viability and induced cell death in a concentration-dependent manner. At a moderate concentration (~20 μM), MDL-12330A mainly induced apoptotic death whereas at concentrations greater than 20 μM, it increased non-apoptotic cell death. The induction of apoptosis was at least partially regulated by CHOP-mediated DR5 upregulation, as detected by immunoblotting and gene interference assays. More importantly, low concentrations of MDL-12330A effectively enhanced recombinant human tumor necrosis factor (TNF)-related apoptosis-inducing ligand (rhTRAIL)-induced apoptosis and clonogenicity in these gastric cancer cells. This study demonstrates a possible role of MDL-12330A as a potential sensitizer to TRAIL, and suggests a novel therapeutic strategy targeting gastric cancer cells.
机译:MDL-12330A是广泛使用的腺苷酸环化酶(AC)抑制剂,可阻止AC / cAMP信号传导。在这项研究中,我们证明了这种药物在胃癌(GC)细胞系中的新型抗肿瘤活性。在这些GC细胞中,MDL-12330A以浓度依赖的方式降低了细胞活力并诱导了细胞死亡。在中等浓度(〜20μM)下,MDL-12330A主要诱导细胞凋亡死亡,而在浓度大于20μM时,其增加非凋亡细胞死亡。如通过免疫印迹和基因干扰测定所检测的,凋亡的诱导至少部分地由CHOP介导的DR5上调调节。更重要的是,低浓度的MDL-12330A有效增强了重组人肿瘤坏死因子(TNF)相关的凋亡诱导配体(rhTRAIL)诱导的这些胃癌细胞的凋亡和克隆形成能力。这项研究证明了MDL-12330A作为TRAIL的潜在敏化剂的可能作用,并提出了针对胃癌细胞的新型治疗策略。

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