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DEK的表达与结直肠癌患者预后的相关性研究 被引量:2

Expression and prognostic significance of DEK in human colorectal carcinoma
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摘要 目的:采用免疫组化技术,分析DEK基因在结直肠癌患者中的表达情况及其与预后的相关性。方法:运用免疫组化SP法,检测DEK基因在169例结直肠癌患者肿瘤组织及癌旁组织中的表达情况,并运用统计分析软件分析DEK表达水平与结直肠癌患者预后的相关性。结果:DEK的表达率在结直肠癌组织(85/169,50.30%)明显高于癌旁正常组织(28/169,16.57%),差异具有统计学意义(P<0.01)。DEK在肿瘤组织中的表达情况与病人年龄、性别、肿瘤分化程度、TNM分期及肿瘤大小等因素无相关性,与总生存率(OS)显著相关(P<0.05)。结论:DEK表达水平与结直肠癌预后密切相关,DEK高表达的结直肠癌患者预后较差。 Objective :To analyze DEK gene expression and prognostic significance in human colorectal carcinoma by using immunohistochemical techniques. Methods :Immunohistochemical SP method was used to test the expression of DEK gene in 169 eases of colorectal cancer tissue and para - carcinoma tissue, and statistical analysis software was used to analyze the correlation between DEK gene expression and prognostic significance in human colorectal carcino- ma. Results:The expression rate of DEK in colorectal cancer tissue 85/169 (50.30%) was significantly higher than those in para - carcinoma tissue,28/169 ( 16.57% ) ( P 〈 0.01 ). The level of DEK expression in the tumor tissues was irrelevant to age, gender, differentiated degree, TNM stage and location, but significantly correlated with overall survival(OS) ( P 〈 0.05 ). Conclusion: DEK expression is closely related to the prognosis of colorectal cancer. There will be poor prognosis for colorectal cancer patients with high DEK expression.
出处 《现代肿瘤医学》 CAS 2014年第4期875-878,共4页 Journal of Modern Oncology
关键词 DEK 结直肠癌 免疫组化 生存分析 DEK colorectal cancer immunohistochemical survival analysis
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参考文献19

  • 1Wise-Draper TM,Mintz-Cole RA,Morris TA,et al.Overexpression of the cellular DEK protein promotes epithelial transformation in vitro and in vivo[J].Cancer Res,2009,69 (5):1792-1799.
  • 2Wu Q,Li Z,Lin H,et al.DEK overexpression in uterine cervical cancers[J].Pathol Int,2008,58 (6):378-382.
  • 3Orlic M,Spencer CE,Wang L,et al.Expression analysis of 6p22 genomic gain in retinoblastoma[J].Genes Chromosomes Cancer,2006,45 (1):72-82.
  • 4Carro MS,Spiga FM,Quarto M,et al.DEK expression is controlled by E2F and deregulated in diverse tumor types[J].Cell Cycle,2006,5 (11):1202-1207.
  • 5Sanchez-Carbayo M,Socci ND,Lozano JJ,et al.Gene discovery in bladder cancer progression using cDNA microarrays[J].Am J Pathol,2003,163(2):505-516.
  • 6Larramendy ML,Niini T,Elonen E,et al.Overexpression of translocation-associated fusion genes of FGFRI,MYC,NPMI,and DEK,but absence of the translocations in acute myeloid leukemia.A microarray analysis[J].Haematologica,2002,87 (6):569-577.
  • 7Kroes RA,Jastrow A,McLone MG,et al.The identification of novel therapeutic targets for the treatment of malignant brain tumors[J].Cancer Lett,2000,156 (2):191-198.
  • 8Grottke C,Mantwill K,Dietel M,et al.Identification of differentially expressed genes in human melanoma cells with acquired resistance to various antineoplastic drugs[J].Int J Cancer,2000,88 (4):535-546.
  • 9Kondoh N,Wakatsuki T,Ryo A,et al.Identification and characterization of genes associated with human hepatocellular carcinogenesis[J].Cancer Res,1999,59(19):4990-4996.
  • 10Friedrichs K,Gluba S,Eidtmann H,et al.Overexpression of p53 and prognosis in breast cancer[J].Cancer,1993,72:3641-3647.

二级参考文献20

  • 1Tournigand C,Andre T,Achille E,et al.FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer:a randomized GERCOR study[J].J Clin Oncol,2004,22:229 -237.
  • 2Xiong HQ,Ajani JA.Treatment of colorectal cancer metastasis:the role of chemotherapy [J].Cancer Metastasis Rev,2004,23(1 -2):145 -163.
  • 3Kohne CH,van Cutsem E,Wils J,Bokemeyer C,et al.Phase Ⅲ study of weekly high-dose infusional fluorouracil plus folinic acid with or without irinotecan in patients with metastatic colorectal cancer:European Organization for Research and Treatment of Cancer Gastrointestinal Group Study 40986 [J].J Clin Oncol.2005,23 (22) :4856 - 4865.
  • 4Martin MJ.Current stage-specific chemotherapeutic options in colon cancer [J].Expert Rev Anticancer Ther,2005,5 (4):695 -704.
  • 5Grothey A,Deschler B,Kroening H,et al.Phase Ⅲ study of bolus 5-fluorouracil (5-FU)/folinic acid (FA) (Mayo) vs weekly high-dose 24h 5-FU infusion/FA + oxaliplatin (OXA)(FOLFOX) in advanced colorectal cancer (ACRC) [J].Proc Am Soc Clin Oncol,2002,21 :abstr 512.
  • 6Kohne CH,Cutsem VE.Wils JA et al.Irinotecan improves the activity of the AIO regimen in metastatic colorectal cancer:Results of EORTC GI Group study 40986 [J].Proc Am Soc Clin Oncol,2004,23:abstr 1018.
  • 7Saltz LB,Cox JV,Blanke C,et al.Irinotecan plus fluorouracil and leucovorin for metastatic Colorectal cancer.Irinotecan Study Group[J].N Engl J Med,2000,343(13) :905 -914.
  • 8de Gramont A,Figer A,Seymour M,et al.Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer[J].J Clin Oncol,2000,18(16) :2938- 2947.
  • 9de Gramont A,Bosset JF,Milan C,et al.Randomized trial comparing monthly low-dose leucovorin and fluorouracil bolus with bimonthly high-dose leucovorin and fluorouracil bolus plus continuous infusion for advanced colorectal cancer:a French intergroup study[J].J Clin Oncol ,1997,15(2) :808 -815.
  • 10Cunningham D,Humblet Y,Siena S,et al.Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer[J].N Engl J Med,2004,351 (4) :337- 345.

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同被引文献29

  • 1吕自力,文剑明,罗殿中,张文敏,肖刚,张萌.肿瘤相关基因在肝细胞癌及癌旁正常肝组织中表达[J].临床与实验病理学杂志,2004,20(6):654-658. 被引量:4
  • 2汪亚伦,王彤,许凤,冮岩,王杰.伴有6;9染色体易位急性髓系白血病患者DEK-CAN融合基因表达分析[J].中国实验血液学杂志,2006,14(2):232-236. 被引量:8
  • 3Kappes F,Scholten I ,Richter N,et al. Functional do- mains of the ubiquitous chromatin protein DEK[J]. Mol Cell Biol, 2004, 24(13):6 000-6 010.
  • 4Aravind L, Koonin EV. SAP-a putative DNA-hinding motif involved in chromosomai organization[J]. Trends Biochem Sci,2000,25(3) :112-114.
  • 5Waldmann T,Baack M,Richter N,et al. Structure-spe- cific binding of the protooncogene protein DEK to DNA [J]. Nucleic Acids RES, 2003, 31(23):7 003-7 010.
  • 6Alexiadis V, Waldmann T, Andersen J, et al. The pro- tein encoded by the proto-oncogene DEK changes the topology of chromatin and reduces the efficiency of DNA replication in a chromatin-specific manner[J]. Genes Dev,2000,14(ll) :1 308-1 312.
  • 7Wise-Draper TM, Mintz Colr RA, Morris TA, et al. Overexpression of the cellular DEK protein promotes epithelial transformation in vitro and in vivo[J]. Cancer Res,2009,69(5):1 792-1 799.
  • 8Wise-Draper TM, Allen HV, Jones EE, et al. Apop- tosis inhibition by the human DEK oncoprotein involves interference with P53 functions[J]. Mol Cell Biol, 2006, 26(20) :7 506-7 519.
  • 9Secchiero P, Voltan R, Iasio MG, et al. The oncogene DEK promotes leukemic cell survival and is downregu lated by both Nutlin-3 and chlorambucil in B-chronic lymphocytic leukemic cells[J]. Clin Cancer Res,2010, 16(6):1 824-1 833.
  • 10Lee KS, Kim DW, Kim JY, et al. Caspase-dependent apoptosis induction by targeted expression of DEK in- drosophila involves histone acetylation inhibition[J]. J Cell Bioche,2008,1(103) :1 283-1 293.

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