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P53及nm23在不同分子亚型浸润性乳腺癌中的表达及意义 被引量:1

Expression and significance of P53 and nm23 in different molecular subtypes of breast carcinoma
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摘要 目的 :研究P53及nm23在不同分子亚型浸润性乳腺癌中的表达及其意义。方法 :将275例浸润性乳腺癌患者分为激素受体阳性、HER2受体阳性及三阴性3组,采用免疫组织化学法检测其P53及nm23蛋白的表达水平。结果:P53在激素受体阳性组、HER2受体阳性组、三阴性组中的表达率分别为38.9%、73.5%及77.3%,3组间的P53表达有统计学意义差异(χ2=30.662,P<0.05),以三阴性组表达最高;nm23在激素受体阳性组、HER2受体阳性组、三阴性组中的表达率分别为84.3%、67.6%及54.5%,3组间差异有统计学意义(χ2=15.515,P<0.05),以三阴性组及HER2阳性组表达较低。有腋窝淋巴结转移的乳腺癌患者的P53表达阳性率高于无腋窝淋巴结转移者,差异有统计学意义(χ2=5.502,P<0.05);而无腋窝淋巴结转移者的nm23表达阳性率高于有腋窝淋巴结转移者,差异亦有统计学意义(χ2=21.196,P<0.05)。结论:在不同分子亚型的乳腺癌中联合检测P53及nm23,可作为评价乳腺癌发生、发展的指标,更有助于临床治疗和预后判断。 Objective: To investigate the expression and significance of P53 and nm23 in different molecular subtypes of breast carcinoma. Methods: The expression of ER、PR、HER2、P53 and nm23 were detected immunohistochemically in275 specimens of invasive breast carcinoma. Results: Positive expression rates of P53 were 38.9% in ER/PR(+) group,73.5% in HER2(+)group, and 77.3% in triple negative breast cancer group. Significant differences in positive expression rates of P53 between the 3 groups were seen( χ^2=30.662, P 0.05), with the highest expression level in triple negative breast cancer group. The positive expression rates of nm23 were 84.3% in ER/PR(+)group, 67.6% in HER2(+)group and54.5% in triple negative breast cancer group. Significant differences in positive expression rates of nm23 were found be-tween the 3 groups( χ^2=15.515, P〈0.05), and the expression rates were lower in HER2(+) group and triple negative breast cancer group. Patients with axillary lymph nodes metastasis had a higher positive expression rate of P53 than those without axillary lymph nodes metastasis( χ^2=5.502, P〈0.05), while expression of nm23 was the contrary( χ^2=21.196, P〈0.05).Conclusions: Combined detection of P53 and nm23 in breast carcinoma of different molecular subtypes may contribute to the guidance of clinical treatment and prognosis prediction.
作者 高玉霞 沈媛
出处 《诊断学理论与实践》 2015年第1期58-61,共4页 Journal of Diagnostics Concepts & Practice
关键词 P53 NM23 分子亚型 乳腺癌 免疫组织化学 P53 nm23 Molecular subtypes Breast carcinoma Immunohistochemical staining
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参考文献14

  • 1Tavassoli FA, Devilee P. The WHO classification of tumors of the breast and female genital organs[M]. Lyon: IARC Press,2003:10-112.
  • 2乳腺癌HER2检测指南(2014版)[J].中华病理学杂志,2014,43(4):262-267. 被引量:297
  • 3Menendez D, Nguyen TA, Freudenberg JM, et al. Diverse stresses dramatically alter genome-wide p53 binding and transactivation landscape in human cancer cells[J]. Nu- cleic Acids Res,2013,41(15):7286-7301.
  • 4Walerych D, Napoli M, Collavin L, et al. The rebel angel: mutant p53 as the driving oncogene in breast cancer[J]. Carcinogenesis,2012,33(11):2007-2017.
  • 5Varna M, Bousquet G, Plassa LF, et al. TP53 status and response to treatment in breast cancers[J]. J Biomed Biotechnol,2011,2011:284584.
  • 6Bieging KT, Attardi LD. Deconstructing p53 transcrip- tional networks in tumor suppression[J]. Trends Cell Biol, 2012,22(2):97-106.
  • 7Boissan M, Lacombe ML. NM23, an example of a metas- tasis suppressor gene[J]. Bull Caneer,2012,99(4):431-440.
  • 8Cubukcu E, Kanat O, Fatih Olmez O, et al. Prognostic significance of estrogen receptor, progesterone receptor, HER2/neu, Ki-67, and nm23 expression in patients with invasive breast cancer[J]. J BUON,2013,18(2):359-365.
  • 9Rustamadji P. NM23HI as marker of metastasis in inva- sive ductal breast cancer[J]. Acta Med Indones,2012,44(1): 40-46.
  • 10de Ruijter TC, Veeck J, de Hoon JP, et al. Characteris- tics of triple-negative breast cancer[J]. J Cancer Res Clin Oncol,2011,137(2):183-192.

二级参考文献79

  • 1江泽飞,姚开泰,宋三泰.乳腺癌治疗的新循证医学证据和临床实践[J].中华医学杂志,2005,85(43):3025-3027. 被引量:29
  • 2张瑰红,施达仁,梁晓曼,侯景辉,康苏娅,朱卫东,李晓兵,邵云,陈丽荣,周燕.显色原位杂交和免疫组织化学检测乳腺癌HER2/neu基因状况和蛋白表达的对照性研究[J].中华病理学杂志,2006,35(10):580-583. 被引量:29
  • 3<乳腺癌HER2检测指南>编写组,霍临明.乳腺癌HER2检测指南[J].中华病理学杂志,2006,35(10):631-633. 被引量:165
  • 4谢晓冬.常见肿瘤规范化、标准化诊治 第1讲 乳腺癌的化学治疗[J].中国医刊,2007,42(8):33-36. 被引量:2
  • 5Holash J, Maisonpierre P C, Compton D R et al. Vessel cooption, regression, and growth in tumors medisted by angiopoietins and VEGF. Science, 1999, 284:1994
  • 6Kieser A, Weich H A, Brandner G et al. Mutant p53potentiates proteinkinase C induction of vascular endothelial growth factor expression. Oncogene, 1994, 9:963
  • 7Kang S M, Maeda K , Onoda N et al. Combined analysis of p53 and vascular endothelial growth factor expression in colorectal carcinoma for determination of tumor vascularity and liver metastasis. Int J Cancer, 1997,74: 502
  • 8Uchida S, Shimada Y, Watanabe G et al. In oesophageal squamous cell carcinoma vascular endothelial growth factor is associated with p53 mutation, advanced stage and poor prognosis. BJC, 1998, 77: 1704
  • 9Tang R F, Itakura J, Aikawa T et al. Overexpression of lymphangiogenic growth factor VEGF-C in human pancreatic cancer. Pancreas, 2001, 22:285
  • 10Masood R, Cai J, Zheng T et al. Vascular endothelial growth factor/vascular permeability factor is an autocrine growth factor for AIDS-Kaposi sarcoma. Proc Natl Acad Sci USA, 1997, 94:979

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