期刊文献+

混合型肝癌组织中OV_6与Snail蛋白的表达及临床意义 被引量:6

Expression and clinical significance of OV_6 and Snail in mixed hepatocellular cholangiocarcinoma
下载PDF
导出
摘要 目的探讨混合型肝癌中OV6与Snail的表达及临床意义。方法回顾性分析本院1998年4月—2003年7月收治的经病理学诊断确诊为混合型肝癌且行手术切除的70例患者,采用免疫组织化学方法检测肿瘤组织中OV6和Snail蛋白的表达情况,分析其表达水平与临床病理因素及预后的关系。结果 OV6与Snail蛋白阳性表达率分别为42.8%(30/70)和47.1%(33/70);OV6和Snail蛋白的表达均与肿瘤数目、血AFP水平和微血管侵犯密切相关(P<0.05),且都影响患者术后生存(P<0.05)。Snail蛋白的表达还影响患者术后复发(P<0.05)。OV6和Snail在肿瘤中的表达呈正相关(r=0.270,P<0.05)。结论 OV6和Snail在混合型肝癌中的表达状态与肿瘤的发生发展密切相关。 Objective To explore the expression and significance of OV6 and Snail in mixed hepatocellular cholangiocarcinoma.Methods Clinical materials of 70 patients with mixed hepatocellular cholangiocarcinoma and surgical resection were analyzed retrospectively.Expressions of OV6 and Snail were detected by immunohistochemistry in tumor tissue,and the correlation between the expression levels and clinical pathological and prognosis were analyzed.Results The positive rates of OV6 and Snail were 42.8% and 47.1% respectively.The positive expression rates of OV6 and Snail were significantly related with tumor multiplicity,serum levels of oα-fetoprotein and microvascular invasion (P < 0.05),both affected overall survival.The protein expression of Snail also affected disease-free survival (P < 0.0 5).OV6 in tumor liver was associated with expression of Snail (r =0.2 7 0,P <0.05).Conclusion Expressions of OV6 and Snail proteins are associated with clinicopathological development in mixed hepatocellular cholangiocarcinoma.
出处 《实用临床医药杂志》 CAS 2014年第11期17-20,共4页 Journal of Clinical Medicine in Practice
关键词 混合型肝癌 OV6 SNAIL 免疫组化 mixed hepatocellular cholangiocarcinoma OV6 Snail immunohistochemistry
  • 相关文献

同被引文献85

  • 1方瑞,郭强,杜军.高表达Snail蛋白诱导黑色素瘤EMT细胞模型的构建及鉴定[J].中国生物工程杂志,2013,33(7):1-7. 被引量:3
  • 2言伟强,王成林,刘远健,高文清,刘鹏程.肝血管瘤的螺旋CT三期扫描表现分析[J].中国CT和MRI杂志,2004,2(3):34-37. 被引量:19
  • 3赵峰,许顺良,林坚,郑继爱.26例混合细胞性肝癌的CT和MRI诊断[J].中国临床医学影像杂志,2010,21(11):804-806. 被引量:14
  • 4Bo16s V,Peinado H,Prez-Moreno MA,et al. The transcrip- tion factor Slug represses E-cadherin expression and in- duces epithelial to mesenchymal transitions:A comparison with Snail and E47 repressors[J]. J Cell Sci, 2003,116(3): 499-511.
  • 5Jin K, Ewton DZ,Park S,et al. Mirk regulates the exit of colon cancer ceils from quiescence[J]. J Biological Chem- istry, 2009,284(34) : 22916-22925.
  • 6Ye Y, XiaoY, Wang W, et al. ERa signaling through slug regulates E-cadherin and EMTERa signaling regulates E-cadherin through slugfJ]. Oncogene,2010,29(1 O) : 1451- 1462.
  • 7Perez-ManceraPA, Gonzalez-Herrero I, Perez-Caro M, etal. SLUG in cancer developmenltJ} Oncogene,2005,24(19): 3073-3082.
  • 8Nieto MA. The snail superfamily of zinc finger transcrip- tion factors[J]. Nat Rev Mol Cell Biol, 2002,3 (3) : 155- 166.
  • 9Micalizzi DS, Farabaugh SM,Ford HL. Epithelial-mes- enchymal transition in cancer:Parallels between normal development and tumor progression[J]. J Mammary Gland Biol Neoplasia, 2010,15 (2) : 117-134.
  • 10Vetter G, Le B6chec A, Muller J, et al. Time-resolved analysis of transcriptional events during Snail-triggered epithelial to mesenchymal transition[J]. Biochem Biophys Res Commun, 2009,385 (4) : 485-491.

引证文献6

二级引证文献7

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