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乳腺癌组织中Bmi-1蛋白表达与病理学特征的相关性研究 被引量:2

Investigation of the Correlation Between the Expression and Pathological Eharaeteristies of Bmi-1 Protein in Breast Cancer
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摘要 目的研究Bmi-1蛋白在乳腺癌组织中的表达与临床病理学特征的相关性。方法采用免疫组织化学方法检测60例乳腺癌组织中Bmi-l蛋白的表达水平,分析Bmi-1蛋白在乳腺癌组织中的表达,并结合乳腺癌患者的临床病理资料分析与其相关性。结果乳腺癌组织中Bmi-1蛋白的阳性表达率为88.3%,Bmi-1蛋白阳性表达与淋巴结转移、肿瘤大小、远处转移及TNM临床分期密切相关(P<0.05),与ER、PR、CerbB-2等临床病理特征无显著性相关(P>0.05)。结论 Bmi-1蛋白的高表达在乳腺癌的发生、发展和转移中起重要作用,提示Bmi-1可能成为预测乳腺癌高度转移的新标志物。 Objective This study was to investigate the correlation between the expression and pathological charaeteristics of Bmi-1 Protein in breast cancer. Methods The expression of Bmi-1 protein in 60 specimens of breast cancer was detected by immunohistochemistry. The correlation of Bmi 1 expression to clinic pathologic features of breast cancer was analyzed. Results The intensive positive rate of/3mi-1 in breast cancer was 88.3%. The intensive expression of Bmi-i was positively correlated to lymph node metastasis, tumor size, metastasis and Clinical stage (TNM) ( P ( 0. 05 ), but not to estrogen receptor ( ER), progesterone receptor ( PR), and C-erbB-2 expression(P〈0.05). Conclusion The high expression of Bmi-1 protein plays important roles in the development and the metastasis of breast cancer, Bmi-1 may serve as a new molecular marker of metastas is of breast cancer.
机构地区 奉化市人民医院
出处 《成都医学院学报》 CAS 2013年第2期165-167,共3页 Journal of Chengdu Medical College
基金 宁波卫生局宁波科学技术局课题项目(NO:2010A21)
关键词 乳腺癌 免疫组织化学 BMI-1 Breast cancer Immunohistochemistry Bmi-1
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  • 1Park IK, Mora-ison SJ, Clarke MF. Broil, stem cells, and senescence regulation[J]. J Clin Invest, 2004, 113 (2) : 175--179.
  • 2Wang H, Pan K, Zhang HK, et al. Increased polycomb--group oncogene Bmi--1 expression correlates with poor prognosis in hepatocellular carcinoma[J]. J Cancer Res Clin Oncol, 2008, 134(5): 535-541.
  • 3AmesJB, Collett K, Akslen LA. Independent prognostic value of the basal-like phenotype of breast cancer and associations with EGFR and candidate stem cell marker BMI-1[J]. Histopathology, 2008, 52 (3): 370--380.
  • 4Reinisch C, Kandutsch S, Uthman A, et al. Bmi-1: a protein expreesed in stem cell, specialized cells and tumors of the gastrointestinal tract[J]. Histol Histopathol, 2006, 21(11) : 1146-1149.
  • 5Jacobs JJ, Kieboom LK, Marino S, et al. The oncogene and Polycomb-group gene Bmi-1 regxxlates cell proliferation and senescence through the ink4a locus[]]. Nature, 1999, 397(6715): 164-165.
  • 6Tateishi K, Ohta M, Kanai F, et al. Dysregulated expression of stem cell factor Bmil in precancerous lesions of the gastrointestinal tract [J]. Clin Cancer Res, 2006, 12(23): 6960--6967.
  • 7Jacobs ,Scheijen B, VonckenJW, et al. Bmi-1 collaborates with c-myc in tumorigenesis by inhibiting C-myc-induced apoptosis via INK4a/ARF[J]. Genes development, 1999, 13(20):2678--2690.
  • 8Liu JH, Song LB, Zhang X, et al. Bmi-1 expression predicts prognosis for patients with gastric carcinoma[J].J surg Oncol, 2008, 97(3): 267-729.
  • 9Van L M, Verbeek S, Scheijen B, et al. Identification of cooperating oncogenes in E~-myc transgenic mice by provirus tagging [J]. Cell, 1991,65(5):735-752.
  • 10Haupt Y, Alexander W S, Barri G, et al. Novel zinc finger gene implicated as myc collaborator by retrovirally accelerated lymphomagenesis in Eμ-myctransgenic mice [J]. Cell, 1991,65 (5): 753-763.

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