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c-erbB-2、p53、PCNA、ER、PR及TopoⅡ在乳腺癌的表达及其临床意义 被引量:5

Expression of c-erbB-2,p53,PCNA,ER,PR and Topo Ⅱ in breast cancer and its clinical significances
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摘要 目的:探讨c-erbB-2、p53、增殖细胞核抗原(proliferating cell nuc lear antigen,PCNA)和DNA拓扑异构酶Ⅱ(DNAtopoisom eraseⅡ,TopoⅡ)及雌激素受体(estrogen receptor,ER)和孕激素受体(progesterone receptor,PR)在乳腺癌的表达和临床病理关系。方法:89例乳腺癌石蜡切片标本免疫组化EnV ision法染色。结果:c-erbB-2、p53、TopoⅡ和PCNA在乳腺癌的阳性率分别为64.04%、29.21%、55.06%和59.55%,其中c-erbB-2、PCNA在淋巴结有无转移之间表达差异有统计学意义(P<0.05),且PCNA的表达与乳腺浸润性癌的关系密切。而TopoⅡ在淋巴结转移间差异无统计学意义(P>0.05)。结论:c-erbB-2、PCNA可以作为判断乳腺癌患者预后的有效指标,TopoⅡ在乳腺癌中的表达可作为指导乳腺癌化疗的重要指标和判断乳腺癌预后的参考指标。 Objective: To evaluate the chnicopathological significance of expressions of c-erbB-2, p53, proliferating cell nuclear antigen (PCNA) , DNA topoisomerase Ⅱ ( Topo Ⅱ ), estrogen receptor(ER) and progesterone receptor(PR) in breast cancer. Methods : Eighty-nine cases of paraffin-embedded specimens of breast carcinoma were studied by immunohistochemical technique. Results:The positive rates of c-erbB-2, p53, Topo Ⅱ and PCNA were 64.04% ,29.21% ,55.06% , and 59.55% , respectively. The expressions of c- erbB-2, PCNA were positively correlated with lymph node metastases( P 〈 0.05 ) , and there was the closely relationship between PCNA and invasive mammary carcinoma. But there was no relationship between Topo Ⅱ and 1 ymph node metastases( P 〉 0.05 ). Conclusions: The results suggested that c-erbB-2 and PCNA can be effective markers for estimating the prognosis of breast cancer. The expressions of Topo Ⅱ may be useful in predicting prognosis and leading chemotherapy.
作者 张琼 朱玉兆
出处 《蚌埠医学院学报》 CAS 2006年第5期447-450,共4页 Journal of Bengbu Medical College
关键词 乳腺肿瘤 c—erbB-2 P53 增殖细胞核抗原 DNA拓扑异构酶Ⅱ 雌激素受体 孕激素受体 breast neoplasms c-erbB-2 p53 proliferating cell nuclear antigen DNA topoisomerase Ⅱ estrogen receptor progesterone receptor
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  • 1张莉萍.DNA拓朴异构酶及其抑制剂与细胞凋亡[J].国外医学(临床生物化学与检验学分册),1997,18(4):181-183. 被引量:6
  • 2[1]Zhu L, Skoultchi AI. Coordinating cell proliferation and differentiation[J]. Curr Opin Genet Dev, 2001,11(1): 91-95.
  • 3[2]John FB, Joyce AS, Thomas G. In vitro assays used to measure the activity of topoisomerase[J]. Antimicrob Agents Chemther, 1990, 34(1): 1-4.
  • 4[3]Froelich-Ammon SJ, Gale KC, Osheroff N et al. Site-specific cleavage of a DNA Hairpin by Topo Ⅱ[J]. J Biol Chem, 1994,260(10): 7719-7723.
  • 5[5]Champoux JJ. DNA topoisomerases: structure, function, and mechanism[J]. Annu RevBiochem, 2001,70: 369-413.
  • 6[6]Kellner U, Sehested M, Jensen PB et al. Culprit and victim-DNA topoisomerase Ⅱ[J]. LancetOncol, 2002, 3(4): 235-243.
  • 7[7]Bakshi RP, Galande S, Muniyappa K. Functional and regulatory characteristics of eukaryotictype Ⅱ DNA topoisomerase[J]. Crit Rev Biochem Mol Biol, 2001, 36(1):1-5.
  • 8[9]Xinbo Z, Jenn C, Bruce D. Hoechst 33342 induces apoptosis in HL-60 cells and inhibitstopoisomerase Ⅰin vivo[J]. Arch Pathol Lab Med, 1999, 123: 921-926.
  • 9[10]Villman K, Stahl E, Liljegren G et al. Topoisomerase Ⅱ-alpha expression in different cellcycle phases in fresh human breast carcinomas[J]. Mod Pathol, 2002, 15(5): 486-491.
  • 10[11]Nicolletta Z, Alberto M, Patrizia S et al. The 180-kDa isoform of topoisomerase Ⅱ islocalized in the nucleolus and belongs to the structural elements of the nucleolar remnant[J].Experimental Cell Research,1992, 200: 460-467.

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