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Effect of ZGDHu-1 on proliferation and apoptosis of A549 cells in vitro and antitumor activity in vivo / 药学学报
Acta Pharmaceutica Sinica ; (12): 26-34, 2007.
Article in Chinese | WPRIM | ID: wpr-281931
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.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / RNA, Messenger / Random Allocation / Tumor Suppressor Protein p53 / Apoptosis / Proto-Oncogene Proteins c-bcl-2 / Reverse Transcriptase Polymerase Chain Reaction / Xenograft Model Antitumor Assays / Cell Line, Tumor Type of study: Controlled clinical trial Limits: Animals / Female / Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2007 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / RNA, Messenger / Random Allocation / Tumor Suppressor Protein p53 / Apoptosis / Proto-Oncogene Proteins c-bcl-2 / Reverse Transcriptase Polymerase Chain Reaction / Xenograft Model Antitumor Assays / Cell Line, Tumor Type of study: Controlled clinical trial Limits: Animals / Female / Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2007 Type: Article