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原发性胆囊癌组织中细胞凋亡及相关基因蛋白产物的表达 被引量:1

Expression of apoptosis and gene proteins in gallbladder neoplasms and dysplasia
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摘要 目的探讨原发性胆囊癌组织中细胞凋亡及相关基因蛋白Bcl-2及p21WAF1的表达。方法用免疫组化ABC法检测46例原发性胆囊癌不同组织学分级中p21WAF1和Bcl-2的表达,TUNAL法检测细胞凋亡的发生。结果在原发性胆囊癌中随着组织学分级的增加,细胞凋亡率减少,并且p21WAF1表达减弱,而Bcl-2表达增强,差异均有统计学意义(P<0.05);相关分析显示细胞凋亡率与p21WAF1表达呈正相关(r=0.52,P<0.05),与Bcl-2表达呈负相关(r=-0.58,P<0.05)。结论细胞凋亡对原发性胆囊癌的发生发展有着重要影响,p21WAF1及Bcl-2基因参与胆囊癌的发生和发展。 Objective To investigate the effects of apoptosis and related gene p21^WAF1 and Bcl - 2 in the tumorigenesis of primary gallbladder neoplasms. Methods p21^WAF1 and Bcl - 2 were detected by immunohistochemistry and apoptotic ceils were stained in situ by terminal deoxynudeotidyl transferase mediated- dUTP nick end labeling(TUNAL) in 46 cases of primary gallbladder neoplasms with different histological grades. Results Apoptotic index and p21^WAF1 were decreased, but the expression of Bcl-2 was increased with the increasing of the histological grades in primary gallbladder neoplasms (P〈0.05). p21^WAF1 expression was positively and Bcl-2 expression was negatively associated with the rateof apoptosis(r =0.52,P〈0.05; r= -0.58,P〈0.05 respectively). Conclusion It indicates that apoptosis has an important role in the tumorigenesis of primary gallbladder neoplasms, p21^WAF1 and Bcl-2 take part in the occurrence and progression of primary gallbladder neoplasms.
出处 《中国医师进修杂志》 2006年第4期7-8,24,共3页 Chinese Journal of Postgraduates of Medicine
关键词 胆囊癌 凋亡 P21^WAF1 BCL-2 Gallbladder neoplasms Apoptosis p21^WAF1 Bcl- 2
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  • 1Kawamata N,Morosettic R,Miller CW,et al.Molecular analysis of the cyclin-dependent kinase inhibitor gene p27/kipi in human magnancies.Cancer Res,1995,55:2266-2278. 被引量:1
  • 2Goke R,Barth P,Schmidt A,et al.Programmed cell death protein 4 suppresses CDK1/cdc2 via induction of p21 (waf1/cip1).Am J Physiol Cell Physiol,2004,287(6):1541-1546. 被引量:1
  • 3Alenzi FQ,Warrens AN.Cellular and molecular themes in apoptosis.Wien Klin Wochenschr,2003,115:563-574. 被引量:1
  • 4于志勇,左文述,魏玲,薛兴奎,卓培英,宋现让,刘玉谭,刘岩松,周正波,邵志敏.阿霉素对不同乳腺癌细胞株的抑制及凋亡调控作用[J].中华医学杂志,2005,85(1):19-22. 被引量:10
  • 5Ruiz-Ruiz C,Munoz-Pinedo C,Lopez-Rivas A,et al.Interferon-gamma treatment elevates caspase-8 expression and sensitizes human breast tumor cells to a death receptor-induced mitochondria-operated apoptosis program.Cancer Res,2000,60(20):5673-5680. 被引量:1

二级参考文献14

  • 1Ng AY, Bales W, Veltri RW. Phenylbutyrate-induced apoptosis and differential expression of Bcl-2, Bax, p53 and Fas in human prostate cancer cell lines. Anal Quant Cytol Histol,2000,22:45-54. 被引量:1
  • 2Kawanishi S, Hiraku Y. Amplification of anticancer drug-induced DNA damage and apoptosis by DNA-binding compounds. Curr Med Chem Anti-Canc Agents,2004,4:415-419. 被引量:1
  • 3Tsai JY, Safran H. Status of treatment for advanced gastric carcinoma. Curr Oncol Rep,2003,5:210-218. 被引量:1
  • 4Egawa T, Kubota T, Suto A, et al. Docetaxel enhances the cytotoxicity of anthracyclines by increasing intracellular drug accumulation. Oncol Rep,2002,9:777-781. 被引量:1
  • 5Beurel E, Kornprobst M, Blivet-Van Eggelpoel MJ,et al. GSK-3beta inhibition by litbium confers resistance to chemotherapy-induced apoptosis through the repression of CD95 (Fas/APO-1) expression.Exp Cell Res,2004 ,300 :354-364. 被引量:1
  • 6Alenzi FQ, Warrens AN. Cellular and molecular themes in apoptosis. Wien Kiln Wochenschr,2003 ,115 :563-574. 被引量:1
  • 7Han J, Goldstein LA, Gastman BR, et al. Differential involvement of Bax and Bak in TRAIL-mediated apoptosls of leukemic T cells.Leukemia ,2004,18 : 1671-1680. 被引量:1
  • 8Yuki K, Takahashi A, Ota 1, et al. Sensitization by glycerol for CDDP-therapy against human cultured cancer cells and tumors bearing mutated p53 gene. Apoptosis,2004,9:853-859. 被引量:1
  • 9Kigawa J, Sato S, Shimada M, et al. p53 gene status and chemosensitivity in ovarian cancer. Hum Cell,2001,14 : 165-171. 被引量:1
  • 10Zhan M, Yu D, Lang A,et al. Wild type p53 sensitizes soft tissue sarcoma cells to doxorubicin by down-regulating multidrug resistance-1 expression. Cancer,2001,92 : 1556-1566. 被引量:1

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