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Mdm2、p53在乳腺癌中的表达及意义 被引量:2

Expression of P53 and MDM2protein in breast tumor
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摘要 目的研究Mdm2、P53蛋白在乳腺肿瘤组织中的表达及临床意义。方法应用免疫组化SP法检测Mdm2、P53蛋白在不同组织学类型乳腺癌60例、正常乳腺组织20例中的表达。结果Mdm2、P53蛋白在乳腺癌组织中阳性表达率与正常乳腺组织比较差异有统计学意义(P〈0.01)。Mdm2、P53蛋白表达与肿瘤大小比较无差异(P〉0.05),在临床分期、腋窝淋巴结转移之间比较差异有统计学意义(P〈0.01)。结论Mdm2、P53蛋白在乳腺癌组织中的异常表达,说明在乳腺癌的发生及发展中起重要作用。 Objective To investigate the expression of anti-oneogene P53 and caneergeneMDM2 proteins and their significance inthe pathogenesls and progress of Breast tumor. Methods To detect the expression ofP53 andMDM2 in 60 cases of Breast tumor and 20 cases of normal Breast tissue with immunoh is to chemical method. Results The positive rate of P53 in the tissues of the 60 cases of breast tumor is much higher than it in the 20 cases of normal breast tissues. There is statistical significance in the disparity ( P 〈 0. 01 ). Mdm2, P53 protein expression and tumor size was no difference ( P 〉 0. 05 ), clinical stage, axillary lymph node metastasis was significant difference( P 〈 0.01 ). Conclusion Both P53 andMDM2 participate in the pathogenesis and progress of breast tumor and they can be considered as the biological index to evaluate breast tumor.
出处 《中国临床实用医学》 2010年第8期8-9,共2页 China Clinical Practical Medicine
关键词 乳腺肿瘤 MDM2蛋白 P53蛋白 免疫组织化学 P53 MDM2 Breast tumor immunohistoehemistry
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  • 1周承,温廷桓.太湖德永摇蚊过敏的调查[J].寄生虫与医学昆虫学报,1994,1(2):42-47. 被引量:44
  • 2张丽萍,许良中.nm23基因在人体肿瘤研究的现状[J].实用癌症杂志,1995,10(4):281-283. 被引量:9
  • 3赵亚刚,张学庸,惠宏襄,赵永同,王成济.人野生型P53基因真核表达载体的构建及其转染胃癌细胞后对胃癌细胞的影响[J].第四军医大学学报,1996,17(4):300-301. 被引量:4
  • 4Roth JA, Cristiano RJ. Gene therapy for cancer: what have we done and where are we going? J Natl Cancer Inst,1997,89(1):21-39.
  • 5Ramesh R, Saeki T, Templeton NS, et al. Successful treatment of primary and disseminated human lung cancers by systemic delivery of tumor suppressor genes using an improved liposome vector. Mol Ther,2001,3(3):337-350.
  • 6D'Orazi G, Marchetti A, Crescenzi M, et al. Exogenous wt-p53 protein is active in transformed cells but not in their non-transformed counterparts: implications for cancer gene therapy without tumor targeting. J Gene Med,2000,2(1):11-21.
  • 7Zhang WW, Fang X, Mazur W, et al. High-efficiency gene transfer and high-le-vel expression of wild-type p53 in human lung cancer cells mediated by recombinant adenovirus. Cancer Gene Ther,1994,1(1):5-13.
  • 8Osaki S, Nakanishi Y, Takayama K, et al. Alteration of drug chemosensitivity caused by the adenovirus-mediated transfer of the wild-type p53 gene in human lung cancer cells. Cancer Gene Ther,2000,7(2):300-307.
  • 9Horio Y, Hasegawa Y, Sekido Y, et al. Synergistic effects of adenovirus expressing wild-type p53 on chemosensitivity of non-small cell lung cancer cells. Cancer Gene Ther,2000,7(4):537-544.
  • 10Kawabe S, Munshi A, Zumstein LA, et al. Adenovirus-mediated wild-type p53 gene expression radiosensitizes non-small cell lung cancer cells but not normal lung fibroblasts. Int J Radiat Biol,2001,77(2):185-194.

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  • 1Golubovskaya VM, Conway-Dorsey K, Edmiston SN, et al. FAK overexpression and p53 mutations are highly correlated in human breast cancer[J]. Int J Cancer, 2009, 125:1735-1738.
  • 2Olivier M, Eeles R, Hollstein M, et al. The IARC TP53 data- base: new online mutation analysis and recommendations to users [J]. Hum Mutat, 2002, 19:607-614.
  • 3Wickremasinghe RG, Prentice AG, Steele AJ. P53 and Notch sig naling in chronic lymphocytic leukemia: clues to identifying novel therapeutic strategies [ J ]. Leukemia,2011 ;25 ( 9 ) : 1400-1407.
  • 4Meek DW. Tumour suppression by p53 : a role for the DNA dam- age response[J]. Nat Rev Cancer,2009,9(10) :714-723.
  • 5Chang LJ, Eastman A. Decreased translation of p21 (waft) mR- NA causes attenuated p53 signaling in some p53 wild-type tumors [J]. Cell Cycle,2012,11(9):1818-1826.
  • 6Seong HA, Ha H. Murine protein serine/threonine kinase 38 acti- vates p53 function through Serl5 phosphorylation [ J]. J Biol Chem, 2012,15 (25) :20797-20810.
  • 7Yin Y, Luciani MG, Fahraeus. P53 stability and activity is regu- lated by mdm2-mediated induction of alternative p53 translation products[ J]. Nat Cell Biol , 2002,46:462-467.
  • 8Camus S, Menendez S, Fernandes K,et al. The p53 isofomls are differentially modified by MDM2 [ J ]. Cell Cycle, 2012, 11 (8) : 1646-1655.
  • 9Huang L, Yan Z, Liao X, et al. The p53 inhibitors MDM2/MD- MX complex is required for control of p53 activity in vivo [ J ]. Proc Natl Acad Sci USA,2011, 108 ( 29 ) : 12001 - 12006.
  • 10Nicholson J, Hupp TR. The molecular dynamics of MDM2[ J ]. Cell Cycle,2010, 9(10) :1878-1881.

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