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Ad-wtp53对p53状态不同结直肠癌细胞生长的影响
引用本文:阎 昭,李 雯,牛瑞芳,史玉荣,郝希山.Ad-wtp53对p53状态不同结直肠癌细胞生长的影响[J].中国肿瘤生物治疗杂志,2003,10(1):42-47.
作者姓名:阎 昭  李 雯  牛瑞芳  史玉荣  郝希山
作者单位:天津医科大学肿瘤医院,天津,300060
摘    要:目的:探讨胃癌组织中MAGE-1基因启动子B'B区去甲基化状态及其与病理分级及临床分期的关系。方法:取胃癌组织标本40例,另外取同患者相应的癌旁组织40例作为对照。采用分子生物学技术-甲基化敏感性内切酶酶切及PCR扩增技术,研究了胃癌组织中MAGE-1启动子B'B区的去甲基化状态。结果:在所检测的胃癌组织标本中MAGE-1基因启动子B'B区去甲基化的发生率为25%(10/40)。而在癌旁组织中发生率为0,两者发生率的差别具有显著的统计学意义(P<0.01)。在低分化腺癌中MAGE-1基因的B'B区去甲化发生率为50%(6/12),中分化腺癌中发生率为18.7%(3/16),高分化腺癌中发生率为8.3(1/11)。其发生率的差异有统计学意义(P<0.05)。在早期胃癌组织中B'B区的去甲基化的发生率为16.7%,在晚期胃癌组织中发生率为28.6%(P<0.05),差别有统计学意义。结论:胃癌组织中MAGE-1基因启动子的B'B区存在去甲基化。该区的去甲基化发生率与胃癌组织的病理分级以及与临床分期有关。

关 键 词:胃癌  MAGE-1基因启动子  去甲基化
文章编号:1007-385X(2003)01-0039-03
收稿时间:2002/8/25 0:00:00
修稿时间:8/1/2002 12:00:00 AM

The Effects of Recombinant Adenovirus-Mediated Wild Type p53 cDNA on Human Colorectal Cancer Cell Lines with Different p53 Status
YAN Zhao,LI Wen,NIU Rui-fang,SHI Yu-rong and HAO Xi-shan.The Effects of Recombinant Adenovirus-Mediated Wild Type p53 cDNA on Human Colorectal Cancer Cell Lines with Different p53 Status[J].Chinese Journal of Cancer Biotherapy,2003,10(1):42-47.
Authors:YAN Zhao  LI Wen  NIU Rui-fang  SHI Yu-rong and HAO Xi-shan
Institution:Cancer Hospital of Tianjin Medical University, Tianjin 300060;Cancer Hospital of Tianjin Medical University, Tianjin 300060;Cancer Hospital of Tianjin Medical University, Tianjin 300060;Cancer Hospital of Tianjin Medical University, Tianjin 300060;Cancer Hospital of Tianjin Medical University, Tianjin 300060
Abstract:Objective:To explore the inhibition effects of ectogenic wild-type p53 cDNA(Ad-wtp53) on colorectal carcinoma cell lines with different p53 gene status and search for the role of wild type p53 tumor suppressor gene in occurrenc and progress of malignant tumor.Methods:MTT process was taken to choose optimal transfection titre. Three kinds of cell lines(p53 gene deletion, mutation and nomal) were transferred by Ad-wtp53 in optimal titre. The inhibition effects of these cell lines were observed and compared. Results:The best titre is 1000 MOI and p53 gene deletion cell line (THC-8908) shew the highest sensitivity. G1-S transition period blocking effects occurred in all cell lines and G2-M phase regulation effects were not coincidence in three colorectal cell lines. Conclusions:Recombinant adenovirus-mediated wild type p53 gene observably inhibited colorectal carcinoma cell lines growth and proliferation, blocked cell cycle in G0/G1 phase and displayed obvious different actions on G2-M phase among cell lines with different p53 status.
Keywords:gastric carcinoma  MAGE 1 gene promoter  demethylation
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