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103钯放射性支架诱导胆管癌细胞凋亡及对抑癌基因的影响和意义

何贵金 姜维国 郭启勇 纪大伟 顾玺 王柳 赵晓丹 潘春来 李安 许书河 高沁怡

中国医科大学学报2012,Vol.41Issue(12):1099-1101,3.
中国医科大学学报2012,Vol.41Issue(12):1099-1101,3.

103钯放射性支架诱导胆管癌细胞凋亡及对抑癌基因的影响和意义

Significance of 103pd Radioactive Stent Induced Cholangiocarcinoma Cells Apoptosis and Effects on Tumor Suppressor Genes

何贵金 1姜维国 2郭启勇 3纪大伟 1顾玺 1王柳 1赵晓丹 1潘春来 1李安 1许书河 4高沁怡5

作者信息

  • 1. 中国医科大学附属盛京医院普外科,沈阳110004
  • 2. 中国医科大学附属盛京医院病理科,沈阳110004
  • 3. 中国医科大学附属盛京医院放射科,沈阳110004
  • 4. 中国原子能研究院同位素研究室,北京100050
  • 5. 中国医科大学附属第一医院同位素室,沈阳110001
  • 折叠

摘要

Abstract

Objective To investigate the role of tumor suppressor genes {p53 gene) in radioactive induced eholangiocareinoma cells apoptosis. Methods A total of 12 nude mire were randomly divided into 103pd radioactive stent group (n =6) and control group (n -6). Cross-sections were stained by HE for cholangiocarcinoma. The expression of p53 in cholangiocareinoma tissue was detected using in situ hy-bridization, cells with the brow-yellow nucleus after DAB coloration indicates positive staining. Positive rate was analyzed under microscope and apoptosis cell in paraffin-bedding cholangiocarcinoma tissue section was determined using immunohistologic-al staining method. Results Expression of p53 was higher in the 103pd radioactive stent group than that in the control group (P < 0.01). The cholangiocarcinoma cell apoptosis rate was significantly increased in the 103pd radioactive stent group than the control group (P < 0.01). Conclusion These results suggest that p53 gene was increased by 103pd induced chokngiaaremoma cell apoptosis, the, results also show that 103pd radioactive stent can inhibit cholangiocarcinoma cell proliferation.

关键词

p53基因/细胞凋亡/γ射线

Key words

p53 gene/apoptosis/γ-ray

分类

医药卫生

引用本文复制引用

何贵金,姜维国,郭启勇,纪大伟,顾玺,王柳,赵晓丹,潘春来,李安,许书河,高沁怡..103钯放射性支架诱导胆管癌细胞凋亡及对抑癌基因的影响和意义[J].中国医科大学学报,2012,41(12):1099-1101,3.

基金项目

辽宁省自然科学基金资助项目(20042063) (20042063)

辽宁省教育厅高校科研计划(05L445) (05L445)

辽宁省科技计划项目(2006225001-6) (2006225001-6)

沈阳市科技计划项目(F12-193-9-01) (F12-193-9-01)

中国医科大学学报

OA北大核心CSCDCSTPCD

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