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[ZGDHu-1对A549细胞体外增殖和凋亡及体内抗肿瘤活性的影响]

[Effect of ZGDHu-1 on proliferation and apoptosis of A549 cells in vitro and antitumor activity in vivo].

作者信息

Zhou Yong-Lie, Hu Wei-Xiao, Lü Ya-Ping, Qiu Lian-Nü, Wang Wen-Song, Yang Zhong-Yu, Liu Jian-Dong, Rao Guo-Wu

机构信息

Central Laboratory, Zhejiang Provincial People's Hospital, Hangzhou 310014, China.

出版信息

Yao Xue Xue Bao. 2007 Jan;42(1):26-34.

Abstract

This study is to explore the mechanism and effect of N, N'-di-(m-methylphenyl)-3, 6-dimethyl-1, 4-dihydro-1, 2, 4, 5-tetrazine-1, 4-dicarboamide (ZGDHu-1) on proliferation and apoptosis of A549 cells in vitro and on A549 xenograft tumor in nude mice. With different concentrations of ZGDHu-1 at different times were used to treat A549 cells in vitro. The proliferation was determined by living cell count, SRB assay and Brdu-ELISA. Cell apoptosis was determined by cell morphology, DNA agarose gel electrophoresis, DNA content, Annexin V/PI and Hoechst 33258 labeling method. The nude mice model of A549 xenograft tumor was established by subcutaneous inoculation. The suppression activity of ZGDHu-1 by intraperitoneal injection on xenograft mice model was detected. The expressions of bcl-2, bax and p53 gene and protein were analyzed by RT-PCR and flow cytometry. ZGDHu-1 can inhibit A549 cell proliferation viability within a certain range of treating time and does, and a majority of A549 cells were arrested in G2-M phase. The A549 cells apoptosis was confirmed by typical cell morphology, DNA fragment, Sub G1 phase, Hoechst 33258 and Annexin V/PI labeling method with a time and dose related manner. When the xenograft tumor mice model were treated with 10, 20 and 40 mg x kg(-1) ZGDHu-1 for 14 days, the tumor growth inhibition rate were 43.7%, 56.9% and 60.0%, respectively. The expression of bax, bax/bcl-2 and p53 gene and protein increased significantly and bcl-2 decreased slightly by the treatment of ZGDHu-1. ZGDHu-1 can significantly suppress the growth of A549 xenograft tumor in vivo and inhibited proliferation by inducing tumor cell apoptosis in vitro. The mechanism may associate with its up-regulation of bax and p53 during the apoptosis process.

摘要

本研究旨在探讨N,N'-二(间甲苯基)-3,6-二甲基-1,4-二氢-1,2,4,5-四嗪-1,4-二甲酰胺(ZGDHu-1)体外对A549细胞增殖和凋亡以及对裸鼠A549移植瘤的作用机制和效果。采用不同浓度的ZGDHu-1在不同时间体外处理A549细胞。通过活细胞计数、SRB法和Brdu-ELISA法测定细胞增殖。通过细胞形态学、DNA琼脂糖凝胶电泳、DNA含量、Annexin V/PI和Hoechst 33258标记法检测细胞凋亡。通过皮下接种建立A549移植瘤裸鼠模型。检测腹腔注射ZGDHu-1对移植瘤小鼠模型的抑制活性。采用RT-PCR和流式细胞术分析bcl-2、bax和p53基因及蛋白的表达。ZGDHu-1在一定的处理时间和剂量范围内可抑制A549细胞的增殖活力,且多数A549细胞停滞于G2-M期。通过典型的细胞形态学、DNA片段、亚G1期、Hoechst 33258和Annexin V/PI标记法证实A549细胞凋亡呈时间和剂量依赖性。当用10、20和40 mg·kg-1 ZGDHu-1处理移植瘤小鼠模型14天时,肿瘤生长抑制率分别为43.7%、56.9%和60.0%。ZGDHu-1处理后,bax、bax/bcl-2和p53基因及蛋白表达显著增加,bcl-2略有下降。ZGDHu-1可显著抑制体内A549移植瘤的生长,并在体外通过诱导肿瘤细胞凋亡抑制其增殖。其机制可能与其在凋亡过程中上调bax和p53有关。

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