期刊文献+

MCM4与c-erbB-2蛋白在乳腺浸润性导管癌组织中的表达及其临床意义 被引量:2

Expression and clinical significances of MCM4 and c-erbB-2 protein in breast invasive ductal carcinoma
下载PDF
导出
摘要 目的检测MCM4、c-erbB-2蛋白在乳腺浸润性导管癌(IDC)组织中表达的改变及其在癌发生、发展中的作用。方法采用免疫组化SP法检测80例IDC、20例乳腺不典型增生和30例乳腺腺病等非癌病变旁正常乳腺组织中MCM4、c-erbB-2蛋白的表达情况。结果80例IDC、20例不典型增生组织中MCM4蛋白的阳性率分别为86.25%、70%,与正常对照组比较差异极显著(P<0.01)。IDC组织中c-erbB-2蛋白的阳性率为65%,与不典型增生组及正常对照组比较差异显著(P<0.05)。乳腺癌组中MCM4蛋白的阳性表达与组织学分级、TNM分期、淋巴结转移及肿瘤大小有关(P<0.05),与年龄无关。c-erbB-2蛋白的阳性表达与淋巴结转移有关(P<0.05),而与组织学分级、TNM分期、肿瘤大小及年龄无关。MCM4蛋白的阳性表达与c-erbB-2的表达呈正相关(r=0.240,P<0.05)。结论MCM4蛋白阳性表达可作为乳腺癌发生、发展的生物学指标,联合c-erbB-2检测有助于乳腺癌预后的判断及临床治疗的指导。 Objective To evaluate the significance of MCM4 and c-erbB-2 protein expression and the correlations with carcinogenesis and progression in breast invasive ductal carcinoma. Methods The SP technique was used to detect the expression of MCM4 and c-erbB-2 in 80 cases of breast invasive ductal carcinoma, 20 cases of atypical hyperplasia and 30 cases of normal breast tissues of non-cancerous breast disease. Results The positive rates of MCM4 in 80 cases of breast invasive duetal carcinoma and 20 atypical hyperplasia were 86.25% (69/80) and 70.00% (14/20) respectively, which were significantly higher than those in normal breast tissues ( P 〈 0.001 ). The positivity rate of c-erbB-2 in breast invasive ductal carcinoma was 65.00% (52/80), which was significantly higher than those in atypical hypetplasia and normal breast tissues ( P 〈 0.05). In breast invasive ductal carcinoma, MCM4 protein positive expression was associated with histological grading, clinical stage, lymph node status and ttunor size ( P 〈 0.05), but no correlation with age ( P 〉 0.05). C-erbB-2 positive expression was associated with lymph node status ( P 〈 0.05) , and no correlation with histological grading, clinical stage, tumor size and age (P〉0.05). There was positive correlation between the expression of MCM4 and c-erbB-2 (r = 0.240, P 〈 0.05). Conclusion The expression of MCM4 protein is an objective biologic marker for estimating the occurrence and progression of breast cancer. Combined detection of MCM4 and e-erbB-2 may help judge the prognosis and guide clinical treatment of breast cancer.
出处 《诊断病理学杂志》 CSCD 2009年第6期465-468,共4页 Chinese Journal of Diagnostic Pathology
基金 广西卫生厅医疗卫生科研课题项目(Z2004094)
关键词 乳腺 浸润性导管癌 MCM4 c—erbB-2 免疫组化 Breast Invasive ductal carcinoma MCM4 C-erbB-2 Immunohistochemistry
  • 相关文献

参考文献10

  • 1Stoeber K, Tlsty TD, Happerfield L, et al. DNA replication licensing and human cell proliferation [J]. J Cell Sci, 2001, 114 (Pt11): 2027-2041.
  • 2Lawson JS, Tran D, Rawlinson WD. From Bittner to Barr: a viral, diet and hormone breast cancer aetiology hypothesis [ J]. Breast Cancer Res, 2001, 3(2): 81- 85.
  • 3任占平.微小染色体维持蛋白与肿瘤[J].诊断病理学杂志,2004,11(6):427-429. 被引量:12
  • 4Pasion SG, Forshurg SL. Deconstructing a conserved protein family: the role of MCM proteins in eukaryotie DNA replication [J]. Genet Eng, 2001, 23: 129- 155.
  • 5Labib K, Kearsey SE, Diffley JF. MCM2-7 proteins are essential components of prereplicative complexes that accumulate cooperatively in the nucleus during Gl-phase and are required to establish, but not maintain, the S-phase checkpoint [J]. Mol Biol Cell, 2001, 12(11): 3658-3667.
  • 6Ishimi Y, Okayasu I, Kato C, et al. Enhanced expression of MCM proteins in cancer cells derived from uterine cervix [ J ]. Eur J Biochem, 2003, 270(6): 1089- 1101.
  • 7黄晓平,张旭,苏晓东,马国伟,赵进明,戎铁华.MCM4在食管癌组织中的表达与临床病理的关系[J].癌症,2007,26(1):96-99. 被引量:12
  • 8Volpi A, Nannl O, De Paola F, et al. HER-2 expression and cell proliferation: prognostic markers in patients with node-negative breast cancer [J]. J Clin Oncol, 2003, 21(14): 2708-2712.
  • 9Rodins K, Cheale M, Coleman N, et al. Minichromosome maintenance protein expression in normal kidney and renal cell carcinomas: relationship to tumor dormancy and potential clinical utility [J]. Clin Cancer Res, 2002, 8(4) : 1075 - 1081.
  • 10Kato H, Miyazaki T, Fukai Y, et al. A new proliferation marker, minichromosome maintenance protein 2, is associated with tumor aggressiveness in esophageal squamous cell carcinoma [J]. J Surg Oncol, 2003, 84(1): 24-30.

二级参考文献20

  • 1刘复兴,黄晓平,赵春霞,徐昕,韩亚玲,蔡岩,吴人亮,吴昕,詹启敏,王明荣.食管鳞癌FHIT基因等位缺失及其表达下调[J].癌症,2004,23(9):992-998. 被引量:10
  • 2Gozuacik D,Chami M,Lagorce D, et al. Identification and functional characterization of a new member of the human Mcm protein family:hMcm8 [J]. Nucleic Acids Res,2003,32(2):570-579.
  • 3Going JJ, Keith WN, Neilson L, et al. Aberrant expression of minichromosome maintenance proteins 2 and 5,and Ki-67 in dysplastic squamous oesophageal epithelium and Barrett' s mucosa [J]. Gut,2002,50(3) :373 - 377.
  • 4Labib K,TerceroJA, Diffley JF. Uninterrupted Mom2-7 functionrequired for DNA replication fork progression [J]. Science, 2000, 288(5471): 1643 - 1647.
  • 5Crevel G, Ivetic A, Ohno K, et al. Nearest neighbour analysis of Mcm protein complexes in drosophilia melanogaster [J]. Nucl Acids Res,2001,29(23) :4834 - 4842.
  • 6Lee JK, Hurwitz J. Processive DNA helicase activity of the minichromosome maintenance protein 4,6,and 7 complex requires forked DNA structures [J]. Proc Natl Acad Sci USA,2001,98(1):54- 59.
  • 7YouZ,IshimiY,MasaiH, etal. Roles of Mcm7 andMcm4subunits in the DNA helicase activity of the mouse Mcm4/6/7 complex [J]. J Biol Chem,2002,277(45):42471-42479.
  • 8Ishimi Y. A DNA helicase activity is associated with an Mcm4,-6,and -7 protein complex [J]. J Biol Chem, 1997,272 (39): 24508-24513.
  • 9Ohtani K, Iwanaga R, Nakamura M, et al. Cell growth-regulated expression of mammalian Mcm5 and Mcm6 genes mediated by the transcription factor E2F [J]. Oncogene, 1999,18(14) :2299 - 2309.
  • 10Stemer JM, Dew KS, Musahl C, et al. Negative regulation of DNA replication by the retinoblastoma protein is mediated by its association with Mcm7 [J]. Mol Cell Biol,1998,18(5) :2748- 2757.

共引文献19

同被引文献89

  • 1孔丽凤,赵峰,李景英,房新志.ERβ、C-erbB-2在乳腺癌组织中的表达及其与内分泌治疗效果的关系[J].新疆医科大学学报,2008,31(12):1667-1670. 被引量:3
  • 2周宗炎.C-erbB-2、P53、ki67、ER和PR在乳腺癌中的表达及意义[J].贵州医药,2011,35(2):118-120. 被引量:9
  • 3黄晓平,张旭,苏晓东,马国伟,赵进明,戎铁华.MCM4在食管癌组织中的表达与临床病理的关系[J].癌症,2007,26(1):96-99. 被引量:12
  • 4石华山,李妍,任德莲.C-erbB-2癌基因与NSCLC的研究进展[J].细胞与分子免疫学杂志,2007,23(5):482-483. 被引量:2
  • 5Maine GT Sinha P,Tye BK. Mutants of S. cerevisiae defective in the maintenance of minichromosomes[J]. Genetica, 1984,106(3) :365- 385.
  • 6Kearsey SE,Labib K. MCM proteins:evolution,proterties and role in DNA replication[J]. Biochim Biophys Acta, 1998,1398 : 113-136.
  • 7You Z, Ishimi Y, Masai H, et al. Roles of MCM7 and MC M4 subunits DNA helicase activity of the mouse MCM4/6/7 complex[J]. Biol Chem, 2002,277 (45) : 42471-42479.
  • 8Poplawski A,Crabnwski B,Long SE,et al. The tine finger domain of the archaeal minichromosome maintenance is required for helicase ac- tivity[J]. J Biol Chem, 2001,276 (52) :49371-49377.
  • 9Musahl C,Holthoff HP,Lesch R,et al. Stability of the replicative MCM3 protein in proliferating and differentiating human cells[J]. Exp Cell Res, 1998,241 : 260-264.
  • 10Labib K,Kearsey SE,Diffley JF. MCM2-7 proteins are essentialcomponents of prereplicative complexes that accumulate cooperatively in the nucleus during Gl-phase and are required to establish,but not maintain, the S-phase checkpoint[J]. Mol Biol Cell, 2001,12 ( 11 ) : 3658-3667.

引证文献2

二级引证文献1

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