期刊文献+

DPC4/SMAD4在子宫内膜癌中的表达及意义 被引量:2

Expression of Smad4 protein in endometrial carcinoma and its significance
下载PDF
导出
摘要 目的探讨Smad4蛋白在子宫内膜癌中的表达情况及其意义。方法应用免疫组织化学SP方法检测 56例子宫内膜癌Smad4的表达情况,并与 30例正常子宫内膜和 42例各型增生性子宫内膜对比。结果Smad4在子宫内膜癌中的表达明显低于正常子宫内膜和单纯性增生性子宫内膜(P<0. 01,P<0. 05),且与组织学分级及临床分期明显相关 (P<0. 01,P<0. 05),而与肌层浸润深度无关。结论Smad4蛋白的表达可能在子宫内膜癌的发生发展及判断预后方面具有重要作用,可作为重要的生物学标记物。 Objective To investigate the expression of in endometrial carcinoma and its clinical significance. Methods Smad4 protein was detected in 56 endometrial carcinoma samples and 72 normal or/and benign hypertrophic endometrium samples by immunohistochemical SP method. Results Compared with normal controls and single hyperplasia, Smad4 protein was decreased in endometrial carcinoma tissue (P<0.01, P<0.05). The expression of Smad4 was correlated with histological grade and clinical stage (P<0.01, P<0.05),while no significant difference was detected in tumors of different myometrial carcinoma samples. Conclusion Smad4 protein may play an important role in the development and prognosis of endometrial carcinoma. It may be used as an important biological marker in endometrial carcinoma.
出处 《广东药学院学报》 CAS 2005年第1期89-91,共3页 Academic Journal of Guangdong College of Pharmacy
关键词 SMAD4蛋白 子宫内膜癌 免疫组织化学 Smad4 protein endometrial carcinoma immunohistochemistry
  • 相关文献

参考文献7

  • 1Enomoto T, Fujita M, Inoue M, et al. Alterations of the p53 tumor suppressor gene and its association with activation of the c-K-ras-2 protooncogene in premalignant and malignant lesions of the human uterine endometrium[J]. Cancer Res, 1993,53(8):1 883.
  • 2Hruban RH, Offerhaus GJA, Kern SE, et al. Tumor-suppressor genes in pancreatic cancer[J]. J Hepatobiliary Pancreat Surg, 1998,5:383.
  • 3Pasche B. Role of transforming growth factor beta in cancer[J]. J Cell Physiol, 2001, 186(2): 153.
  • 4Wilentz RE, Su GH, Dai JL, et al. Immunohistochemical labeling for dpc4 mirrors genetic status in pancreatic adenocarcinomas: a new marker of DPC4 inactivation[J]. Am J Pathol, 2000,156(1):37.
  • 5Massague J, Chen YG. Controlling TGF-beta signaling[J]. Genes Dev, 2000 , 14(6):627 .
  • 6Kim YH,Lee HS,Lee HJ,et al. Prognostic significance of the expression of smad4 and Smad7 in human gastric carcinomas[J]. Annals of Oncology,2004,15(1):574.
  • 7Sohn TA, Su GH, Ryu B, et al. High-throughput drug screening of the DPC4 tumor-suppressor pathway in human pancreatic cancer cells[J]. Ann Surg, 2001 ,233(5):696.

同被引文献13

  • 1董蕾,吴强,胡向阳,丁向东,汪渊,杨枫,左莉.涎腺腺样囊性癌组织中内皮细胞特异性分子-1与E钙黏着蛋白的表达[J].安徽医科大学学报,2006,41(4):383-386. 被引量:1
  • 2Hirayama D, Fujinori T, Satonata K, et al. Immunohistochemical study of epidermal growth factor and transforming growth factorβ in penetrating type of early gastric cancer [J]. Human Pathol,1992,23(6) :681.
  • 3Korchynskyi O, Landstrom M, Stoika R, et al. Expression of smad protein in human colorectal cancer [ J ]. Int J Cancer, 1999,82(2) :197.
  • 4Hahn SA, Schuhe M, Hoque ATMS, et al. Dpc4 a candidate tumor suppressor gene at human chromosome 18q21.1 [ J ]. Science, 1996,271 (5247) :350.
  • 5Kaminska B, Wesolowska A, Danilkiewicz M. TGF β signalling and its role in tumour pahtogenesis [ J ]. Acta Biochim Pol,2005,52 (2) :329.
  • 6Minoru F, Tatsuya M, Yasuyuki F, et al. Plasma level of transforming growth factorβ1 measured from the azygos vein predicts prognosis in patients with esophageal cancer[ J]. Clin Cancer Res ,2004,10:2738.
  • 7Liu Y,Zhong X,Li W,et al. The role of Spl in the differential expression of transforming growth factor β receptor type Ⅱ in human breast adenocarcinoma MCF-7 cells[ J]. J Biol Chem,2000,275 (16) : 12231.
  • 8Frnk SP, Swinler SE, Lutterbaugh JD, et al. Transforming growth factor-β induced growth inhibition in a Smad4 mutant colon adenoma cell line [ J ]. Cancer Res, 2001,61 (1) :256.
  • 9Christina H, Miriam B, Juergen D, et al. Smad4-expression is decreased in breast cancer tissues:a retrospective study [ J]. BMC Cancer Res,2006 ,6 :25.
  • 10Hazelbag S, Fleuren GJ, Baelde J J, et al. Cytokine profile of cervical cancer cells[ J]. Gynecol Oncol,2001,83 (2) :235.

引证文献2

二级引证文献11

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