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肿瘤坏死因子相关诱导凋亡配体受体mRNA在肝癌中的表达及其意义 被引量:3

The expression and significance of TRAIL recepters mRNA in hepatocellular carcinoma
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摘要 目的探讨肿瘤坏死因子相关诱导凋亡配体的4种受体DR4、DR5、DcR1、DcR2在肝细胞癌肝组织中的表达状况。方法应用半定量逆转录聚合酶链反应(RTPCR)方法检测40例人肝细胞癌组织、相应癌旁肝组织、23例正常人肝组织中DR4、DR5、DcR1、DcR2的mRNA表达率及表达水平。结果(1)40例肝癌组织、癌旁组织、23例正常肝组织DR4、DR5的mRNA的表达水平差异无统计学意义(P>0.05);(2)40例癌旁组织、23例正常肝组织DcR1、DcR2表达水平明显高于40例肝癌组织(P<0.05);(3)DR4和DR5mRNA在肝细胞癌组织中表达水平与患者的年龄,肿瘤大小,有无包膜,分级程度,AFP水平,HBsAg,有无肝硬化有关系。结论肝癌组织中存在TRAIL受体的表达,与其在正常肝组织中的表达差异有统计学意义(P<0.05);DR4、DR5表达水平与肝癌的病理状况有关系。 Objective To explore the mechanism and clinical significance of TRAIL-induced apoptosis in hepatocellular carcinoma (HCC) by detecting the expression of DR4, DR5, DcR1 and DcR2 mRNA, the main recepters of the TRAIL, in liver tissue of patients with HCC. Methods DR4, DR5, DcR1 and DcR2 mRNA expression and its levels were assessed in 23 cases of normal liver tissue, 40 cases of para-liver cancer tissuse and 40 cases of HCC tissues with semi-quantitative reverse transcription polymerase chain reation (RT-PCR) method. Results (1) There was no different expression levels of DR4 and DR5mRNA among the normal liver tissue, para-liver cancer tissuse and HCC tissue (P 〉 0.05);(2) The positive expression level of DcR1 and DcR2 mRNA in the normal liver tissue and para-liver cancer tissuse was significant1:, higher than in HCC tissue (P 〈 0.05);(3) Statistical correlation hmong the expression changes of DR4 or DR5 mRNA and patient' s age, size and differentiation of the tumor, plasma AFP levels and HBsAg was existed. Conclusion TRAIL receptors expression was prevalent in HCC, which was different from that in normal liver tissue;The expression of DR4 or DR5 was closely correlated with HCC pathological status.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2005年第10期1214-1216,共3页 Chinese Journal of Experimental Surgery
关键词 肿瘤坏死因子 凋亡配体受体 MRNA 肝癌 基因表达 Carcinoma, hepatocellular IRAIL recepters PCR
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  • 1Pan G, O'Rourke K, Chinnaiyan AM, et al. The receptor for the cytotoxic ligand TRAIL[J]. Science, 1997, 276:111-113. 被引量:1
  • 2Motzer RJ, Bander NH, Nanus DM. Renal-cell carcinoma. N Engl J Med, 1996, 335: 865-887. 被引量:1
  • 3Wu XX, Mizutani Y, Kakehi Y, et al. Expression of major histocompatibility complex antigens and adhesion molecules on renal cell carcinoma cells, and effect of interferon-α and/or cimetidine on the expression. Acta Urol Jpn, 1998,44: 621-626. 被引量:1
  • 4Lin Y, Devn A, Cook A, et al. The death domain kinase RIP is essential for TRAIL (Apo2L)-induced activation of I B kinase and c-Jun N-Terminal Kinase. Mol Cell Biol, 2000, 20: 6638-6645. 被引量:1
  • 5MacFarrlane M. TRAIL-induced signallling and apoptosis. Toxicol Lett, 2003, 139: 89-97. 被引量:1
  • 6Rossi D, Gaidano G. Messengers of cell death: apoptotic signaling in health and disease. Haematologica, 2003, 88 ; 212-218. 被引量:1
  • 7Wu XX, Kakehi Y, Mizutani Y, et al. Enhancement of TRAIL/Apo2L-mediated apoptosis by adriamycin through inducing DR4 and DR5 in renal cell carcinoma cells. Int J Cancer, 2003, 104 : 409-417. 被引量:1
  • 8Shigeno M, Nakao K, Ichikawa T, et al. Interferon-a sensitizes human hepatoma cells to TRAIL-induced apoptosis through DR5 upregulation and NF-κB inactivation. Oncogene, 2003, 22:1653-1662. 被引量:1
  • 9Pan H;Rourke K;chinnaiyan AM.The receptor for the cytotoxic ligand TRAIL[J],1997(5309). 被引量:5
  • 10Wiley SR;Schooley K;Smolak PJ.Identification and characterization of a new member of the TNF family that induces apoptosis[J],1995. 被引量:1

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  • 1张仲宁,喻爱喜,侯炜,祝少博,程丽,毛琳.肿瘤坏死因子相关凋亡诱导配体联合阿霉素治疗骨肉瘤[J].中华实验外科杂志,2006,23(2):141-143. 被引量:6
  • 2朱冉旭,林菊生,宋宇虎,黎培员,陶璐薇.死亡受体5与肝癌细胞凋亡的相关性[J].中华肿瘤杂志,2006,28(4):261-264. 被引量:6
  • 3佟海侠,张继红,马力,陆春伟,张锦华.Caspase-8和DR5在TRAIL诱导神经母细胞瘤细胞凋亡中的作用[J].中国当代儿科杂志,2006,8(4):327-330. 被引量:4
  • 4Wiley SR,Schooley K,Smolak PJ.Identification and characterizationof a new member of the TNF family that induees apoptosis.Immunity,1995,3:673-682. 被引量:1
  • 5Falschlehner C ’Schaefer U ’ Walczak H.Following TRAIL’ s path inthe immune system.Immunology,2009,127:145-154. 被引量:1
  • 6Gray HL,Sorensen EL,Hunt JS,et al.Three polymorphisms in the 3 ’UTR of the TRAIL(TNF-related apoptosis-inducing ligand)gene.Genes Immun,2001,2:469-470. 被引量:1
  • 7Goldstraw P,Crowley J,Chansky K,et ai.The IASLC Lung CancerStaging Project:proposals for the revision of the TNM stage groupingsin the forthcoming(seventh)edition of the TNM Classification of ma-lignant tumours.J Thorac Oncol,2007,2:706-714. 被引量:1
  • 8Yan X,Xu L,Qi J,et al.sTRAIL levels and TRAIL gene polymor-phisms in Chinese patients with fatty liver disease.Immunogenetics,2009,61:551-556. 被引量:1
  • 9Lub-de HMN,de Vries EG,de Jong S,et al.Soluble TRAIL concen-trations are raised in patients with systemic lupus erythematosus.AnnRheum Dis,2005,64 ; 854-858. 被引量:1
  • 10Kikuchi S,Miyagishi R,Fukazawa T,et al.TNF-related apoptosis in-ducing ligand(TRAIL)gene polymorphism in Japanese patients withmultiple sclerosis.J Neuroimmunol,2005,167:170-174. 被引量:1

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