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IKKε在卵巢癌中的表达及临床意义 被引量:3

Expression and clinical significance of IKKε in ovarian cancer
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摘要 目的探讨I-κB激酶ε(IKKε)在卵巢癌组织中的表达及与卵巢癌转移的关系。方法采用实时定量PCR(qRT-PCR)和Western blot法分别检测53例不同临床分期的卵巢癌组织和10例正常卵巢组织中IKKεmRNA和蛋白表达,并分析IKKε表达与卵巢癌转移的相关性。结果Ⅱ、Ⅲ、Ⅳ期卵巢癌组织中IKKεmRNA和蛋白表达高于正常卵巢组织和Ⅰ期卵巢癌组织(P<0.05),且IKKε表达随着卵巢癌临床分期升高而增加(P<0.05),但与卵巢癌的病理类型、组织学分型及年龄无明显相关性(P>0.05)。结论 IKKε表达与卵巢癌的临床分期密切相关,可望成为临床治疗卵巢癌的一个新靶点。 Objective To investigate I-kB kinase ε(IKKε) expression in ovarian Cancer tissues and its correlation with tumor metastasis. Methods The mRNA and protein expressions of IKKε were detected by quantitative RT-PCR and Western blot in 53 cases of ovarian cancer in different clinical stages and 10 cases of normal ovarian tissues, respectively. Then the correlation between the expressions and ovarian cancer metastasis was analyzed. Results The mRNA and protein expressions of IKKε in ovarian cancer in stage Ⅲ-Ⅳ were significantly higher than those in ovarian cancer in stage I and normal ovarian tissues (P〈0. 05). IKKε expression was up-regulated with the increase of clinical stages of ovarian cancer (P〈0. 05 ), but had no significant correlation with pathological pattern, histological classification and age (P〈0. 05). Conclusion IKKε expression is closely correlated with clinical stages of ovarian cancer, which may be taken as a new target for the treatment of ovarian cancer in the future.
作者 成开花
出处 《江苏医药》 CAS 北大核心 2014年第1期63-66,共4页 Jiangsu Medical Journal
关键词 I-kB激酶ε 卵巢癌 I-kB kinase εOvarian cancer
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参考文献12

  • 1黄光琦,贺国丽,宋毅.几种肿瘤转移基因变化与卵巢癌转移的相关性[J].华西医科大学学报,2002,33(1):28-31. 被引量:4
  • 2Tenoever BR,Ng SL,Chua MA. Multiple functions of the IKK-related kinase IKKepsilon in interferon-mediated antiviral immunity[J].{H}SCIENCE,2007,(5816):1274-1278.
  • 3Boehm JS,Zhao J J,Yao J. Integrative genomic approaches identify IKBKE as a breast cancer oncogene[J].{H}CELL,2007,(06):1065-1079.
  • 4Hsu S,Kim M,Hernandez L. IKK-ε coordinates invasion and metastasis of ovarian cancer[J].{H}CANCER RESEARCH,2012,(21):5494-5504.
  • 5Ozols RF,Bookman MA,Connolly DC. Focus on epithelial ovarian cancer[J].{H}CANCER CELLS,2004,(01):19-24.
  • 6Chau TL,Gioia R,Gatot JS. Are the IKKs and IKK-related kinases TBK1 and IKK-epsilon similarly activated[J].{H}Trends in Biochemical Sciences,2008,(04):171-180.
  • 7Boehm JS,Zhao J J,Yao J. Integrative genomic approaches identify IKBKE as a breast cancer oncogene[J].{H}CELL,2007,(06):1065-1079.
  • 8Xie X,Zhang D,Zhao B. IkappaB kinase epsilon and TANK-binding kinase 1 activate AKT by direct phosphorylation[J].{H}Proceedings of the National Academy of Sciences(USA),2011,(16):6474-6479.
  • 9Shen RR,Zhou AY,Kim E. IκB kinase ε phosphorylates TRAF2 to promote mammary epithelial cell transformation[J].{H}Molecular and Cellular Biology,2012,(23):4756-4768.
  • 10Guo JP,Shu SK,He L. Deregulation of IKBKE is associated with tumor progression,poor prognosis,and cisplatin resistance in ovarian cancer[J].{H}AMERICAN JOURNAL OF PATHOLOGY,2009,(01):324-333.

二级参考文献10

  • 1[1]Sawan A. Lascul, Veron M, et al. NDPK/nm23 expressi on in human breast cancer in relation to relapse, survival, and other prognostic factors: an immunohisto-chemical study. J Pathology, 1994; 172 (1):27
  • 2[2]Shiozaki H, Tahara H, Oka H, et al. Expression of immunoreact ive E-cadherin adhesion molecules in human cancer. Am J Pathol, 1991; 139 (1): 17
  • 3[3]Toh Y, Pencil SD, Nicolson GL, A Novel cndidate metastasis-assoc iated gene, mtal, differentially expressed in high metastatic mammary adenocarci noma cell line. J Biological Chemistry, 1994; 269(37):22958
  • 4[4]Toh Y, oki E, Ods S, et al. Overexpressionof MTA1 gene in ga strointestinal carcinoma: correlation with invasion and metastasis. Int J Cancer , 1997; 74(4):459
  • 5[5]Toh Y, Kiwano H, Mori M, et al. Overexpression of met astasis -associated MTA1 mRNA in invasive oesophageal carcinomas. Br J Cancer, 1999; 79 (11-12): 1723
  • 6[6]Tokunaga Y, Urano T, Furukawa K, et al. Reduced expre ssion of nm23H1 but not of nm23H2, is concordant with the freguency of lymph-node m etastasis of human breast cancer. Int J Cancer, 1993; 55(3):66
  • 7[7]Berx G, Staes K, Van Hengel J, et al. Cloning and cha racterzi tion of the human invasion suppressor gene E-cadherin(CDHI). Genomics, 1995; 26 :(2)281
  • 8[8]Toh Y, Kuninaka S, Endo K, et al Molecular analysis o f a cand idate metastasis-associated, MTA1: possible inferaction with histone deacetylas e 1. J Exp Clin Cancer Res, 2000;19(1):105
  • 9[9]Lakshmi MS, Parker C, Sherbet GV .Metastasis associated m tsl and nm23 gene affect tubulin polymerization II in B16 melanomas: a possible mechanis m of their regulation of metastasis behaviour of tumors. Anticancer Res, 1993; 1 3(2):299
  • 10[10]Shapiro L, Fannon AM, Kwong PD, et al. Structural base of ce ll-adhesion by cadherin. Nature.,1995;374(23):327

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  • 1Boehm JS, Zhao JJ, Yao J, et al. Integrative genomicapproaches identify IKBKE as a breast cancer oncogene[J].Cell,2007,129(6) :1065-1079.
  • 2Peters RT, Liao SM,Maniatis T. IKKepsilon is part of a novelPMA-inducible IkappaB kinase complex[J]. Mol Cell,2000,5(3):513-522.
  • 3Harris J,Oliere S, Sharma S, et al. Nuclear accumulation ofcRel following C-terminal phosphorylation byTBKl/IKKepsilon[J]. J Immunol, 2006,177(4): 2527-2535.
  • 4Gilmore TD, Wolenski FS. NF-kB: where did it come fromand why[J]. Immunol Rev,2012,246(1) : 14-35.
  • 5Hutti JE,Shen RR, Abbott DW,et al. Phosphorylation of thetumor suppressor CYLD by the breast canceroncogeneIKKepsilon promotes cell transformation[J]. Mol Cell,2009,34(4):461-472.
  • 6Shen RR,Zhou AY,Kim E,et al. I.cB kinase e phosphorylatesTRAF2 to promote mammary epithelial celltransformation[J]. Mol Cell Biol,2012,32(23) :4756-4768.
  • 7Reiley W, Zhang M, Wu X, et al. Regulation of thedeubiquitinating enzyme CYLD by IkappaB kinasegamma-dependent phosphorylation[J], Mol Cell Biol* 2005, 25 ( 10):3886-3895.
  • 8Guo JP,Coppola D, Cheng JQ. IKBKE protein activates Aktindependent of phosphatidylinositol 3-kinase/PDKl/mTORC2 and the pleckstrin homology domain tosustainmalignant transformation[J].J Biol Chem, 2011, 286(43):37389-37398.
  • 9Kim HS, Lee MS. ST ATI as a key modulator of cell death[J].Cell Signal,2007,19(3) =454-465.
  • 10Yarilina A,Park-Min KH, Antoniv T,et al. TNF activates anIRFl-dependent autocrine loop leading to sustainedexpressionof chemokines and ST ATI-dependent type I interferon-response genes[J]. Nat Immunol,2008.9.4) :378-387.

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