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人乳癌组织中血管生成素-2及其受体Tie-2的表达 被引量:5

Expression of angiopoietin-2 and Tie-2 in human breast cancer tissue
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摘要 目的:探讨乳癌组织中血管生成素-2(Ang-2)、血管生成素2受体Tie-2的表达。方法:应用免疫组化SP法检测28例人乳腺导管内癌、49例浸润性导管癌、25例乳腺纤维腺瘤和51例正常乳腺间质组织中Ang2及Tie-2、CD34的表达,根据CD34的表达情况计算微血管密度(MVD)。结果:正常乳腺间质组织中Ang-2、Tie-2阳性表达率分别为12.0%(6/50)和18.0%(9/50),在乳腺纤维腺瘤组织中的阳性表达率为16.0%(4/25)和20.0%(5/25);而在乳腺导管内癌组织中的阳性表达率分别为53.57%(15/28)和64.28%(18/28),在乳腺浸润性导管癌组织中的表达率分别为93.87%(46/49)和97.96%(48/49),均显著高于正常乳腺间质组织和乳腺纤维腺瘤组织中的表达(P<0.01)。乳癌组织CD34的表达显著高于其在正常乳腺间质组织中的表达。结论:Ang2及Tie2的表达与乳癌血管生成关系密切,Ang2表达与乳癌的浸润有关。 Aim : To explore the expression and significance of Angiopoietin-2 and Tie-2 in breast cancer tissue. Methods:The expressions of Ang-2, Tie-2, CD34 were detected by immunohistochemistry SP method in 28 cases of intraductal carcinoma in situ, 49 cases of invasive ductal carcinoma, 25 cases of fibroadenoma of breast, and 50 cases of normal mammary tissue. The microvessel density (MVD) of the normal and tumor tissue based on the expression of CD34 was calculated and analyzed the relation between the pathological character of mammary cancer. Results: The positive rate of Ang-2 and Tie-2 in the normal mammary stroma, fibroadenoma of breast, intraductal carcinoma in situ and invasive duetal carcinoma were 12.0% and 18.0% , 16.0% and 20.0% , 53.57% and 64.28% , 93.87% and 97.96% , respectively. The expression levels of Ang-2 and Tie-2 in carcinoma tissue were significantly higher than those in normal tissue and fibroadenoma of breast ( P 〈0.01 ). The expression level of CD34 in carcinoma tissue was significantly higher than that in normal tissue. Conclusion : The expressions of Ang-2 and Tie-2 have intimate correlation with the sprouting new vessel of mammary cancer. The expression of Ang-2 is connected with the nature of breast tumor and the metastasis of breast cancer.
出处 《郑州大学学报(医学版)》 CAS 北大核心 2006年第3期517-519,共3页 Journal of Zhengzhou University(Medical Sciences)
关键词 乳腺肿瘤 血管生成素-2 血管生成素-2受体 微血管密度 breast neoplasm angiopoietin-2 Tie-2 MVD
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  • 1Stratmann A, Risau W, Plate KH. Cell type-specific expression of angiopoietin-1 and angiopoietin-2 suggests a role in glioblastoma angiogenesis. Am J Pathol 1998; 153:1459-1466.
  • 2Newland RC, Dent OF, Lyttle MN, Chapuis PH, Bokey EL.Pathologic determinants of survival associated with colorectal cancer with lymph node metastases. A multivariate analysis of 579 patients. Cancer 1994; 73:2076-2082.
  • 3Steinberg SM, Barwick KW, Stablein DM. Importance of tumor pathology and morphology in patients with surgically resected colon cancer. Cancer 1986; 58:1340-1345.
  • 4Mustonen T, Alitalo K. Endothelial receptor tyrosine kinases involved in angiogenesis. J Cell Biol 1995; 129:895-898.
  • 5Maisonpierre PC, Goldfarb M, Yancopoulos GD, Gao G.Distinct rat genes with related profiles of expression define a TIE receptor tyrosine kinase family. Oncolgene 1993; 7: 1631-1637.
  • 6Sato TN, Qin Y, Kozak CA, Audus KL. Tie-1 and tie-2 define another class of putative receptor tyrosine kinase genes expressed in early embryonic vascular system. Proc Natl Acad Sci USA 1993; 90:9355-9358.
  • 7Dumont DJ, Gradwohl G, Fong GH, Puri MC, Gertsenstein M, Auerbach A, Breitman ML. Dominant-negative and targeted null mutations in the endothelial reeptor tyrosine kinase,tek, reveal a critical role in vasculogenesis of the embryo.Genes Development 1994; 8:1897-1909.
  • 8Sato TN, Tozawa Y, Deutsch U, Wolburg-Buchholz K,Fujiwara Y, Gendron-Maguire M, Gridley T, Wolburg H, Risau W, Qin Y. Distinct roles of the receptor tyrosine kinases Tie-1 and Tie-2 in blood vessel formation. Nature 1995; 376:70-74.
  • 9Wong AL, Haroon ZA, Werner S, Dewhirst MW, Greenberg CS, Peters KG. Tie2 expression and phosphorylation in angioenic and quiescent adult tissues. Circ Res 1997; 81:567-574.
  • 10Koblizek TI, Runting AS, Stacker SA, Wilks AF, Risau W,Deutsch U. Tie2 receptor expression and phosphorylation in cultured cells and mouse tissues. Eur J Biochem 1997; 244:774-779.

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