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乳腺浸润性导管癌组织Bmi-1的表达及其临床意义

Expression and clinicopathological relevance of Bmi-1 in invasive mammary ductal cancer
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摘要 目的:探讨Bmi-1在乳腺浸润性导管癌组织中的表达及其与临床病理特征的关系。方法:免疫组化法检测84例乳腺癌组织中雌激素受体(ER)、孕激素受体(PR)、c-erbB-2和B细胞特异性莫洛尼小鼠白血病病毒整合位点-1(Bmi-1)表达,并取其中43例(51.2%)乳腺癌新鲜肿瘤组织和癌旁的正常组织,采用RT-PCR方法检测其Bmi-1表达。结果:84例乳腺浸润性导管癌组织中Bmi-1蛋白阳性表达率为56.0%(47/84)。43例乳腺癌新鲜肿瘤组织中Bmi-1mRNA阳性表达率为67.4%(29/43)。Bmi-1过表达与临床晚期及ER阴性表达显著相关,P<0.05。Bmi-1表达与患者年龄、肿瘤大小、组织学分级以及PR、c-erbB-2表达均无明显相关性,P>0.05。Bmi-1在乳腺浸润性导管癌与癌旁正常组织中的表达差异有统计学意义,P<0.01。结论:Bmi-1过表达与乳腺浸润性导管癌的发生、发展有关。Bmi-1可能成为预测乳腺浸润性导管癌临床分期的新分子标志。 OBJECTIVE:To investigate the relationship between the expression of Bmi-1 and clinicopathological characteristics in invasive mammary ductal cancer.METHODS: Immunohistochemistry was used to detect the expression of ER,PR,c-erbB-2 and Bmi-1 oncoproteins in 84 cases of invasive mammary ductal carcinoma.RT-PCR assay was used to detect the mRNA expression level of Bmi-1 in 43 cases(51.2% from the 84 cases) of breast cancer and paraneoplastic tissues.RESULTS: The positive rate of Bmi-1 oncoprotein expression was 56.0%(47/84) in 84 cases of mammary carcinoma.The positive rate of Bmi-1 mRNA expression was 67.4%(29/43) for the 43 cases of fresh breast cancer tissue samples.The overexpression of Bmi-1 was positively correlated with clinical advanced stage and negative ER status(P0.05),but not with age,tumor size,histological grading,and PR,c-erbB-2(P0.05).Significant different expression of Bmi-1 were found between breast cancer and in paraneoplastic tissues(P0.01).CONCLUSIONS: The intensive expression of Bmi-1 is related to the development and progression of invasive mammary ductal carcinoma.Bmi-1 may serve as a new molecular marker of clinical staging for invasive mammary ductal carcinoma.
出处 《中华肿瘤防治杂志》 CAS 2011年第17期1363-1366,共4页 Chinese Journal of Cancer Prevention and Treatment
基金 南通市社会发展科技计划项目(S2008013)
关键词 乳腺肿瘤 蛋白质类 免疫组织化学 逆转录聚合酶链反应 breast neoplasms proteins immunohistochemistry reverse transcriptase polymerase chain reaction
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参考文献11

  • 1Vonlanthen S, Heighway J, Altermatt H J, et al. The Bmi-1 oncogene induces telomerase activity and immortalizes human mammary epithelial cells[J]. Cancer Res, 2002, 62 (16):4736-4745.
  • 2Hino M,Kobayashi S,Arata K.Reactions of butane and isobutene catalyzed by zirconium oxide treated with sulphate ion.solid superacid catalyst[J].J Am Chem Soc,1979,101(21):6439-6441.
  • 3张锐,刘耀芳.水对SO_4^(2-)/ZrO_2型固体超强酸催化正戊烷异构化反应的影响[J].石油与天然气化工,2000,29(2):53-55. 被引量:4
  • 4李贵新,郭璐,李鹏鑫,路中,孙秀梅,马长庚,刘康,刘锦.乳腺癌组织p53和nm23及VEGF表达相关性的研究[J].中华肿瘤防治杂志,2010,17(12):923-925. 被引量:10
  • 5刘卫红,孟秀香,刘丹丹,单路娟,赵心宇.反义Bmi-1对Jurkat细胞的抑制作用[J].中华血液学杂志,2005,26(9):554-556. 被引量:19
  • 6Jacobs J J, Scheijen B, Voncken J W, et al. Bmi-1 collaborates with c-myc in tumorigenesis by inhibiting c-myc-induced apopto sis viaINK4a/ARF[J]. GenesDev, 1999, 13(20) :2678-2690.
  • 7Kim J H, Yoon S Y, Jeong S H, et al. Overexpression of Bmi-1 oncoprotein correlates with axillary lymph node metastases in in vasive ductal breast cancer[J]. Breast, 2004,13(5) :383-388.
  • 8李嗣杰,韩冰,吴迪.乳腺癌组织中Bmi-1、EZH2蛋白的表达变化及意义[J].山东医药,2010,50(34):49-50. 被引量:4
  • 9Silva J, Garcia V, Garcia J M, et al. Circulating Bmi-1 mRNA as a possible prognostic factor for advanced breast cancer pa- tients[J]. Breast Cancer Res, 2007,9(4):R55.
  • 10Liu W L, Guo X Z, Zhang L J, et al. Prognostic relevance of Bmi-1 expression and autoantibodies in esophageal squamous cell carcinoma[J]. BMC Cancer, 2010,1(10) :467.

二级参考文献26

  • 1刘进,薛新波.P53、VEGF和VEGF-C在胰腺癌中的表达及意义[J].华中科技大学学报(医学版),2004,33(4):472-474. 被引量:7
  • 2Brown L F, Berse B, Jackman K W, et al. Expression vascular permeability factor(vascular endothelial growth factor)and its receptors in adenocarcinomas of the gastrointestinal tract [J].Cancer Res,1993,53(19) :4727-4735.
  • 3Zolota V, Gerokosta A, Melachrinou M, et al. Microvessel density, proliferating activity,p53 and bcl 2 exp ression in situ duc talcarcinoma of thebreast[J].Anticancer Res, 1999, 19(4B) 3269- 3274.
  • 4Toi M, Hoshina S, Takayanagi T, et al. Association of vascular endothelial growth factor expression with tumor angiogenesis and with early relapse in primary breast cancer[J].Jpn J Cancer Res, 1994,85 (10) 1045-1049.
  • 5Tanigawa N,Matsumura M,Amaya H,et al. Tumor vascularity correlates with the prognosis of patients with esophageal Squamous cell carcinoma[J]. Cancer, 1997,79(2) :220-225.
  • 6Folkman J. Tumor angiogenesis: therapeutic implications[J]. N Engl J Med, 1971,285(21) :1182-1186.
  • 7Gautam A, Densmore C L, Melton S, et al. Aerosol delivery of PEI- p53 complexes inhibits B16-F10 lung metastases through regulation of angiogenesis[J].Cancer Gene Ther, 2002,9(1) :28.
  • 8Weinstat-Saslow D L, Zabrenetzky V S, Vanhoutte K, et al. Transfection of thrombospondin-1 complementary DNA into hu man breast carcinoma cell line reduces primary tumor growth, metastatic potential,and angiogenesis[J]. Cancer Res, 1994,54 (24) :6504-6511.
  • 9Ringrose L,Paro R.Epigenetic regulation of cellular memory by the polycomb and trithorax group proteins[J].Annu Rev Genet,2004,38(11):413-443.
  • 10Jacobs JJ,Kieboom K,Marino S,et al.The oncogene and Polycomb-group gene bmi-1 regulates cell proliferation and senescence through the ink4a locus[J].Nature,1999,397(6715):164-168.

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