期刊文献+

CDC25C蛋白和CLDN6蛋白在肝细胞癌中的表达及临床意义 被引量:10

Expression of CDC25C and CLDN6 proteins in hepatic cell carcinoma and its clinical significance
下载PDF
导出
摘要 目的:研究肝细胞癌(hepatic cell carcinoma,HCC)组织中细胞分裂周期蛋白25同源蛋白C(cell division cyclin 25 homolog C,CDC25C)与紧密连接蛋白Claudin-6(CLDN6)的表达情况,探讨其与HCC的发生、发展、预后的关系。方法:应用免疫组织化学SABC法检测58例HCC、24例癌旁组织和18例正常肝脏组织中CDC25C和CLDN6的表达情况,并分析两者与临床病理特征和术后无瘤生存期的关系。结果:CDC25C在HCC组织、癌旁组织、正常肝脏组织表达阳性率分别为86.2%、45.8%、11.1%,表达差异均有统计学意义(P<0.05)。CDC25C在HCC组织中的表达与乙型肝炎表面抗原(HBsAg)、肿瘤直径大小和肿瘤分化程度有关(P<0.05)。CLDN6在HCC组织、癌旁组织、正常肝脏组织表达阳性率分别为77.6%、41.7%、16.7%,表达差异均有统计学意义(P<0.05)。CLDN6在HCC组织中的表达与肿瘤直径大小有关(P<0.05)。HCC中CDC25C阳性组及CDC25C阴性组的中位无瘤生存时间分别为12个月和15个月,差异有统计学意义(P<0.05)。CLDN6阳性组及CLDN6阴性组中位无瘤生存时间分别为12个月和14个月,差异有统计学意义(P<0.05)。结论:CDC25C和CLDN6可能在肝细胞癌的发生、发展及复发过程中起重要作用,有望成为肝癌诊断及预测预后的重要指标。 Objective: To study the expression of cell division cyclin 25 homolog C (CDC25C) and Claudin-6(CLDN6) proteins in hepatic cell carcinoma(HCC) and discuss its clinical significance with the occurrence, development and prognosis of HCC. Methods: Immunohistochemical SABC method was performed to detect the expression of CDC25C and CLDN6 proteins in 58 cases of HCC tissues, 24 cases of tumor-adjacent tissues and 18 cases of normal liver tissues. The relationship between clinical pathological characteristics and postoperative disease-free survival time was ana- lyzed. Results: The expression positive rates of CDC25C in HCC tissues, tumor-adjacent tissues and normal liver tissues were 86.2% , 45.8% , 11.1%. The differences were statistically signifi- eant(P 〈0.05). The expression of CDC25C in HCC tissues was closely related to HBsAg, tumor size and tumor differentiation degree(P 〈 0.05). The positive expression rates of CLDN6 in HCC tissues, tumor-adjacent tissues and normal liver tissues were 77.6% , 41.7% , 16.7% , the differ- ences were statistically significant (P 〈 0.05 ). The expression of CLDN6 in HCC tissues was closely related to tumor differentiation degree (P 〈 0.05 ). The median disease-free survival time of CDC25C positive and negative groups was 12 months and 15 months respectively, the differences were statistically significant(P 〈 0.05). The median disease-free survival time of CLDN6 positive and negative groups were 12 months and 14 months respectively. The differences were statistically significant(P 〈 0.05). Conclusion: CDC25C and CLDN6 may play important roles in the proces- ses of the occurrence, development and recurrence of HCC. They are expected to be the important indicators for diagnosis and prognosis of HCC.
出处 《河南医学研究》 CAS 2013年第6期807-811,共5页 Henan Medical Research
关键词 肝细胞癌 细胞分裂周期蛋白25同源蛋白C 紧密连接蛋白Claudin-6 临床意义 hepatic cell carcinoma CDC25C CLDN6 clinical significance
  • 相关文献

参考文献15

  • 1Aressy B, Ducommun B. Cell cycle control by the CDC25 phosphata- ses [J]. Anticancer Agents Med Chem, 2008, 8 (8): 818-824.
  • 2Boutros R., Lobjuls V, Duenmmun B. CDC25 phosphatases in cancer cells: key players? Good targets? [ J]. Nat Rev Cancer, 2007, 7 ( 7 ) : 495-507.
  • 3Turowski P, Franckhauser C, Morris M C, et al. Functional cdc25C dual-specificity phosphatase is required for S-phase entry in human ceils [J]. Mol Biol Cell, 2003, 14(7) : 2984-2998.
  • 4Lindqvist A, van Zon W, Karlsson Rosenthal C, et al. Cyclin B1- Cdkl activation continues after eentrosome separation to control mitotic progression [J]. PLoS Biol, 2007, 5(5): e123.
  • 5Peng C Y, Graves P R, Thoma R S, et al. Mitotic and G2 checkpoint control: regulation of 14-3-3 protein binding by phosphorylation of Cdc25C on serine-216 [J]. Science, 1997, 277(5331): 1501- 1505.
  • 6Karlsson-Rosenthal C, Millar J B. Cdc25 : mechanisms of checkpoint inhibition and recovery [J]. Trends Cell Biol, 2006, 16(6) : 285-292.
  • 7Ozen M, Ittmann M. Increased expression and activity of CDC25 phosphatase and an alternatively spliced variant in prostate cancer [J]. Clin CancerRes, 2005, 11(13):4701-4706.
  • 8Wang Z, Trope C G, Flcrenes V A, et al. Overexpression of CDC25B, CDC25C and phospho-CDC25C (Ser216) in vulvar squa- mous cell carcinomas are associated with malignant features and ag- gressive cancer phenotypes[J]. BMC Cancer, 2010, 10: 233.
  • 9张强,张仲富,丁宇,周立军,蔡志明.CDC25C基因在肾透明细胞癌中的表达及临床意义[J].安徽医科大学学报,2012,47(11):1336-1339. 被引量:6
  • 10Wang X, Zhao H, Xu Q, et al. HPtaa database-potential target genes for clinical diagnosis and immunotherapy of human carcinoma [ J ]. Nucleic Acids Res, 2006, 34: D607-D612.

二级参考文献15

  • 1许良中,杨文涛.免疫组织化学反应结果的判断标准[J].中国癌症杂志,1996,6(4):229-231. 被引量:1365
  • 2Jemal A, Bray F, Center M M, et al. Global cancer statistics [J]. CA Cancer J Clin, 2011,61(2) : 69 -90.
  • 3Chow W H, Dong L M, Devesa S S, et al. Epidemiology and risk factors for kidney cancer[J]. Nat Rev Urol, 2010,7(5) : 245 - 57.
  • 4Aressy B, Ducommun B, Ducommun, et al. Cell cycle control by the CDC25 phosphatases [ J]. Anticancer Agents Med Chem, 2008,8(8) : 818 -24.
  • 5Boutros R, Lobjois V, Ducommun B. CDC25 phosphatases in cancer cells: key players? good targets? [ J]. Nat Rev Cancer, 2007,7(7) : 495 -507.
  • 6Ozen M, htmann M. Increased expression and activity of CDC25C phosphatase and an alternatively spliced variant in prostate cancer [J]. Clin Cancer Res, 2005,11(13) : 4701 -6.
  • 7Wang Z, Trope G G, Florenes U A, et al. Overexpression of CDC25B, CDC25C and phospho-CDC25C (Ser216) in vulvar squamous cell carcinomas are associated with malignant features and aggressive cancer phenotypes [ J ]. BMC Cancer, 2010,10: 233.
  • 8Turowski P, Franckhauser C, Morris M C, et al. Functional cdc25C dual-specificity phosphatase is required for S-phase entryin human cells[J]. Mol Biol Cell, 2003,14(7) : 2984 -98.
  • 9Lindqvist A, van Zon W, Karlsson Rosenthal C, et al. Cyclin B1- Cdkl activation continues after centrosome separation to control mitotic progression [ J ]. PLoS Biol, 2007,5 ( 5 ) : e123.
  • 10Peng C Y, Graves P R, Thoma R S, et al. Mitotic and G2 check- point control: regulation of 14-3-3 protein binding by phosphoryla- tion of Cdc25C on serine-216 [ J ]. Science, 1997,277 (5331) : 1501 -5.

共引文献5

同被引文献89

引证文献10

二级引证文献15

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