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首页> 外文期刊>Oncology reports >N,N '-di-(m-methylphenyi)-3,6-dimethyl-1,4-dihydro-1,2,4,5-tetrazine-1,4-dicarboamide (ZGDHu-1) suppresses the proliferation of PANC-1 pancreatic cancer cells via apoptosis and G2/M cell cycle arrest
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N,N '-di-(m-methylphenyi)-3,6-dimethyl-1,4-dihydro-1,2,4,5-tetrazine-1,4-dicarboamide (ZGDHu-1) suppresses the proliferation of PANC-1 pancreatic cancer cells via apoptosis and G2/M cell cycle arrest

机译:N,N'-二-(间-甲基苯乙)-3,6-二甲基-1,4-二氢-1,2,4,5-四嗪-1,4-二糖酰胺(ZGDHu-1)抑制PANC的增殖-1胰腺癌细胞通过凋亡和G2 / M细胞周期阻滞

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Pancreatic cancer is one of the human gastrointestinal malignancies with a high mortality and poor prognosis. Approximately eighty percent of patients are diagnosed with unresectable or metastatic disease. Thus, development of novel chemicals in the treatment of pancreatic cancer is imperative. This study aimed to investigate the anticancer effects of N,N'-di-(m-methylphenyi)-3,6-dimethyl-1,4-dihydro-1,2,4,5-tetra- zine-1,4-dicarboamide (ZGDHu-1), a new tetrazine derivative, on the PANC-1 pancreatic cancer cell line and clarify the underlying molecular mechanism. Using an MTT assay, we found that ZGDHu-1 significantly suppressed the proliferation of PANC-1 cells in a time- and dose-dependent manner. Moreover, according to the morphological and flow cytometric analysis, the results indicated that ZGDHu-1 induced PANC-1 cell apoptosis and G2/M cell cycle arrest in a dose-dependent manner. In the western blot analysis, expression of the proapoptotic Bax gene was upregulated while the anti-apoptotic Bcl-2 gene was downregulated following treatment with ZGDHu-1. ZGDHu-1 also activated pro-caspase-3 and PARP and increased the expression of NF-kappa B inhibitor I kappa B. Furthermore, the expression levels of G2/M regulatory molecules such as cyclin B1 and cdc2 were decreased while that of Chk1 was increased. These results suggested that ZGDHu-1 suppressed the proliferation of pancreatic cancer cells, rendering it a potential therapeutic drug for the treatment of pancreatic cancer.
机译:胰腺癌是人类胃肠道恶性肿瘤之一,死亡率高,预后差。大约百分之八十的患者被诊断出患有不可切除或转移性疾病。因此,开发用于治疗胰腺癌的新型化学物质势在必行。这项研究旨在研究N,N'-二-(间甲基苯甲酰基)-3,6-二甲基-1,4-二氢-1,2-,4,5-四嗪-1,4-的抗癌作用二氨基甲酰胺(ZGDHu-1)是一种新的四嗪衍生物,可作用于PANC-1胰腺癌细胞系,并阐明其潜在的分子机制。使用MTT分析,我们发现ZGDHu-1以时间和剂量依赖性方式显着抑制了PANC-1细胞的增殖。此外,根据形态学和流式细胞术分析,结果表明ZGDHu-1以剂量依赖性方式诱导PANC-1细胞凋亡和G2 / M细胞周期停滞。在蛋白质印迹分析中,在用ZGDHu-1处理后,促凋亡的Bax基因的表达被上调,而抗凋亡的Bcl-2基因的表达被下调。 ZGDHu-1还激活了前胱天蛋白酶-3和PARP,并增加了NF-κB抑制剂IκB的表达。此外,G2 / M调控分子(如细胞周期蛋白B1和cdc2)的表达水平降低,而Chk1的表达则降低了。增加。这些结果表明ZGDHu-1抑制了胰腺癌细胞的增殖,使其成为治疗胰腺癌的潜在治疗药物。

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