期刊文献+

胆囊癌WWOX、Survivin表达及相关性研究 被引量:2

下载PDF
导出
摘要 目的观察WWOX、Survivin在胆囊癌中的表达,探讨WWOX和Survivin与胆囊癌的相关性。方法采用免疫组化法检测48例胆囊癌组织、20例癌旁正常胆囊粘膜组织WWOX和Survivin的表达。结果胆囊癌组织中WWOX的阳性表达率显著低于正常胆囊粘膜组织(P<0.01),胆囊癌组织中Survivin的阳性表达率显著高于正常胆囊粘膜组织(P<0.01),胆囊癌中WWOX和Survivin阳性表达率与病理分级、临床分期和淋巴结转移情况相关(P<0.05),WWOX和Survivin在胆囊癌组织中的表达明显负相关(P<0.05)。结论 WWOX和Survivin蛋白异常表达在胆囊癌发生过程中具有重要意义。
出处 《西部医学》 2011年第2期276-277,共2页 Medical Journal of West China
  • 相关文献

参考文献6

  • 1OtKeefe LV, Riehards R I. Common chromosomal fragile sites and cancer:Focus on FRA16D [J]. Cancer Lett, 2006, 232 (1) : 37-47.
  • 2Li F, Altieri DC. The cancer antiapoptosls mouse survlvin genel characterization of locus and transcriptional requirements of basal and cell cycle-dependent expression [J]. Cancer Res, 1999, 59 (13) :3143-3151.
  • 3B EDNAREK A K,LAFLIN K J,DANIEL R L,etal. WWOX,a novel WWdomain- containing protein mapping to human chromosome16q23.3-24.1,a region frequently affected in breast cancer [J]. Cancer Res,2000,60(8) :2140-2145.
  • 4CHANG N S,PRATT N, HEATH J,et al. Hyaluronidase induction of a WW domain-containing oxidoreductase that enhances tumor necrosis factor cytotoxicity[J]. J Biol Chem, 2001, 276 (5) : 3361-3370.
  • 5Suzuki A, Hayashida M,Ito T, et al. Survivin initiates cell cycle entry by the competitive interaction with CDK4/pl 6(INK4a)and CDK2/cyclinE complex activation[J]. Oneogene,2005 ,19(29): 3225-3234.
  • 6Li F, Ambrosini G, Chu E Y, et al. Control of apoptosis and mitotic spindle checkpoint by survivin[J]. Nature, 2006 , 396 (6711):580-584.

同被引文献24

  • 1毕旭东,付晓光,白光.原发性胆囊癌的手术治疗[J].中国普通外科杂志,2005,14(1):68-69. 被引量:14
  • 2Bednarek AK, Laflin K J, Daniel RL, et al. WWOX, a novel WW dom-ain-containing protein mapping to human chromosome 16q23. 3-q24.1,a region frequently affected in breast cancer[ J ]. Cancer Res ,2000,60 ( 8 ) :2140-2145.
  • 3Filling C, Bemdt KD, Benach J, et al. Critical residuces for struc- ture and catalysis in short-chain dehydrogenases/reductases [ J ]. J Biol Chem ,2002,277 (28) :25677-25684.
  • 4Chang NS, Doherty J, Ensign A, et al. WOX1 is essential for tumor necrosis factor, UV light, stanrosporine, and p53-mediated cell death,and its tyrosine 33-phosphorylated form binds and stabilizes serine 46-phosphorylated p53 [ J ]. J Biol Chem, 2005,280 ( 52 ) : 43100-43108.
  • 5Thavathiru E, Ludes-Meyers JH, MacLeod MC, et al. Expression of common chromosomal fragile site genes, WWOX/ FRA16D and FHIT/FRA3B is down regulated by exposure to environmental car- cinogens, UV, and BPDE but not by IR [ J ]. Mol Carcinog, 2005, 44(3) :174-182.
  • 6Aqeilan R1, Donati V, Palamarehuk A, et al. WW domain-contai- ning proteins, Wwox and Yap, compete for interaction with ErbB-4 and modulate its transcriptional function[ J]. Cancer Res ,2005,65 (15) :6764-6772.
  • 7郑运刚,黄昭志,李志愚,何治平,郭丁燕.胆囊癌的早期诊断与处治原则[J].西部医学,2007,19(6):1060-1061. 被引量:1
  • 8Lazcano-Ponce EC, Miquel JF, Mufioz N, et al. Epidemiology and molecular pathology of gallbladder cancer CA Cancer [J]. Clin,2001, 51(6) :349-364.
  • 9Liu JW, Chandra D, Tang SH, Chopra D, Tang DG. Identification and characterization of Bim gamma, anovel proapoptotic BH3-only splice variant of Bim [J]. Cancer Res,2002; 62: 2976-2981.
  • 10Ling MT, Wang X, Ouyang XS, etal. Id-1 expression promotes cell survival through activation of NF-kappaB signalling pathway in pros- tate cancer cells [J]. Oncogene. , 2003,22 (29) : 4498-4508.

引证文献2

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部