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N,N'-二-(间甲基苯基)-3,6-二甲基-1,4-二氢-1,2,4,5-四嗪-1,4-二脒(ZGDHu-1)通过凋亡和 G2/M 细胞周期阻滞抑制 PANC-1 胰腺癌细胞的增殖。

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.

机构信息

Zhejiang Chinese Medical University, Hangzhou, Zhejiang, P.R. China.

Clinical Laboratory Center, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, P.R. China.

出版信息

Oncol Rep. 2015 Apr;33(4):1915-21. doi: 10.3892/or.2015.3803. Epub 2015 Feb 16.

Abstract

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-tetrazine-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 pro-apoptotic 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-κB inhibitor IκB. 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.

摘要

胰腺癌是人类胃肠道恶性肿瘤之一,死亡率高,预后差。大约 80%的患者被诊断为不可切除或转移性疾病。因此,开发治疗胰腺癌的新型化学物质势在必行。本研究旨在探讨新型四嗪衍生物 N,N'-二-(间-甲基苯基)-3,6-二甲基-1,4-二氢-1,2,4,5-四嗪-1,4-二甲酰胺(ZGDHu-1)对 PANC-1 胰腺癌细胞系的抗癌作用,并阐明其潜在的分子机制。采用 MTT 法,我们发现 ZGDHu-1 能显著抑制 PANC-1 细胞的增殖,且呈时间和剂量依赖性。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 Western blot 分析中,用 ZGDHu-1 处理后,促凋亡 Bax 基因表达上调,而抗凋亡 Bcl-2 基因表达下调。ZGDHu-1 还激活了 pro-caspase-3 和 PARP,并增加了 NF-κB 抑制剂 IκB 的表达。此外,G2/M 调节分子如 cyclin B1 和 cdc2 的表达水平降低,而 Chk1 的表达水平升高。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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