期刊文献+

拓扑异构酶Ⅱα表达与乳腺癌患者生存的相关性 被引量:4

Correlation of TOP2A gene expression and survival of breast cancer patients
原文传递
导出
摘要 目的 探讨拓扑异构酶Ⅱα(TOP2A)的表达与乳腺癌患者生存的相关性.方法 通过实时定量逆转录聚合酶链反应(quantitative RT-PCR)方法检测86例乳腺癌组织中的TOP2A基因表达量,应用荧光原位杂交(FISH)检测乳腺癌组织中TOP2A基因扩增,应用免疫组化(IHC)法检测TOP2A蛋白表达,并分析TOP2A基因表达量、TOP2A基因扩增与TOP2A蛋白表达的相关性.结果 86例乳腺癌患者中,TOP2A基因扩增11例,TOP2A基因缺失11例,TOP2A基因变异率为25.6%(22/86);TOP2A蛋白表达的阳性率为66.3%(57/86).TOP2A基因表达水平与蛋白表达水平显著相关(P=0.001),TOP2A基因表达水平与乳腺癌患者的无进展生存期显著相关(P〈0.001).TOP2A基因扩增与TOP2A蛋白阳件表达无显著相关性(P=0.211).结论 TOP2A的基因定量表达水平为乳腺癌客观可靠的临床预后指标. Objective The aim of this study was to assess the TOP2A RNA expression and die relationship of TOP2A protein expression with metastasis-free interval in breast cancer patients. Methods TOP2A expression was analyzed prior to surgery in 86 patients. The level of TOP2A gene amplification was analyzed by fluorescence in situ hybridization (FISH) , its RNA expression level with RT-PCR, and their correlation with TOP2A protein expression was assessed by immunohistochemistry (IHC). The correlation between RNA expression level and metastasis-free interval in breast cancer patients was also analyzed. Results Aberrations (amplification or deletion) of TOP2A copy number was observed in 25.6% (22/86) of the cases. TOP2A protein expression was detected in 66. 3% (57/86) of the samples. There was a significant correlation between the TOP2A RNA expression and protein expression (P〈0.001). TOP2A gene expression was significantly associated with the metastasis-free interval in the breast cancer patients (P =0.001). There was no significant correlation between TOP2A gene amplification and TOP2A protein expression (P=0.211). Conclusions TOP2A RNA level is an objective and reliable prognostic indicator in breast cancer.
出处 《中华肿瘤杂志》 CAS CSCD 北大核心 2011年第5期363-366,共4页 Chinese Journal of Oncology
基金 基金项目:河南省自然科学基金(611040600)
关键词 乳腺肿瘤 拓扑异构酶Ⅱα 荧光原化杂交 实时定量PCR 基因扩增 预后 Breast neoplasms Topoisomerase Ⅱ Alpha Fluorescence in situhybridization Quantitative RT-PCR Gene amplification Prognosis
  • 相关文献

参考文献12

  • 1Brase JC,Schmidt M,Fischbach T,et al.ERBB2 and T0P2A in breast cancer;a comprehensive analysis of gene amplification RNA levels and protein expression and their influence on prognosis and prediction.Clin Cancer Res,2010,16:2391-2401.
  • 2Kwon HC,Roh MS,Oh SY,et al.Prognostic value of expression of ERCCI,thymidylate synthase,and ghtathione S-tramferase PI for 5-fluomuraeil/oxaliplalin chemotherapy in advanced gastric cancer.Ann Oncol,2007,18:504-509.
  • 3Jarvinen TA,Tanner M,Rantanen V,et al.Amplification and deletion of topoisomerase Ⅱ alpha associate with ErbB-2 amplification and affect sensitivity to topoisomerase Ⅱ inhibitor doxorubicin in breast cancer.Am J Pathol,2000,156:839-847.
  • 4<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
  • 5曾瑄,赵大春,周炜洵,武莎斐,梁智勇,刘彤华.荧光原位杂交检测乳腺癌HER2基因状态[J].中华病理学杂志,2005,34(11):701-705. 被引量:65
  • 6杨丽芳,宋三泰,李晓兵,江泽飞,刘晓晴,马维娜,乔西平,郭斯启.284例原发乳腺癌c-erbB2蛋白的表达及其与预后的关系[J].中华肿瘤杂志,2006,28(4):294-297. 被引量:11
  • 7王莉萍,沈坤炜,沈镇宙.赫赛汀在乳腺癌新辅助治疗与辅助治疗中的新进展[J].中华肿瘤杂志,2006,28(4):241-243. 被引量:26
  • 8Orlando L,Del Curto B,Gandini S,et al.Topoisomerase Ⅱ alpha gene status and prediction of pathological complete remission after anthracycline-based neoadjuvant chemotherapy in endocrine non-responsive Her2/neu-positive breast cancer.Breast,2008,17:506-511.
  • 9Tanner M,Isola J,Wiklund T,et al.Topoisomerase Ⅱ alpha gene amplification predicts favorable treatment response to tailored and Jose-escalated anthracycline-based adjuvant chemotherapy in HER-2/neu-amplified breast cancer:Scandinavian Breast Group Trial 9401.J Clin Oncol,2006,24:2428-2436.
  • 10Bhargava R,Lai P,Chen B.HER-2/neu and topoisomerase Ⅱ alpha gene amplification and protein expression in invasive breast carcinomas; chromogenic in situ hybridization and immunohistochemical analyses.Am J Clin Pathol,2005,123:889-895.

二级参考文献51

  • 1宋三泰 汤仲明 等.雌激素受体(ER)阳性乳癌的临床和病理特点的研究[J].中华肿瘤杂志,1985,7(6):426-428.
  • 2Van de Vijver MJ. Assessment of the need and appropriate method for testing for the human epidermal growth factor receptor-2 (HER2).Eur J Cancer, 2001, 37Suppl 1: 11-17.
  • 3Ross JS, Gray GS. Targeted therapy for cancer: the HER-2/neu and Herceptin story. Clin Leadersh Manag Rev, 2003, 17:333-340.
  • 4Vogel-C, Cobieigh MA, Tripathy D? et al. First-line, single-agent Herceptin ( R ) ( trastuzumab ) in metastatic breast cancer: a preliminary report. Eur J Cancer, 2001, 37 Suppl 1:25-29.
  • 5Hammock L, Lewis M, Phillips C, et al. Strong Her-2/neu protein overexpression by immunohistochemistry often does not predict oncogene amplification by fluorescence in situ hybridization. Hum Pathol, 2005,36 : 1043-1047.
  • 6Ross JS, Fletcher JA, Linette GP, et al. The HER-2/neu gene and protein in breast cancer 2003: biomarker and target of therapy.Oncologist, 2003, 8:307-325.
  • 7Hicks DG, Tubbs RR. Assessment of the HER2 status in breast cancer by fluorescence in situ hybridization: a technical review with interpretive guidelines. Hum Pathol, 2005, 36:250-261.
  • 8Yarden Y. Biology of HER2 and its importance in breast cancer.Oncology, 2001, 61 Suppl 2:1-13.
  • 9Reed W, Hannisdal E, Boehler PJ, et al. The prognostic value of p53 and c-erb B-2 immunostaining is overrated for patients with lymph node negative breast carcinoma: a multivariate analysis of prognostic factors in 613 patients with a follow-up of 14-30 years.Cancer, 2000,88:804-813.
  • 10Berry DA, Muss HB, Thor AD, et al. HER-2/neu and p53 expression versus tamoxifen resistance in estrogen receptor-positive,node-positive breast cancer. J Clin Oncol, 2000, 18:3471-3479.

共引文献257

同被引文献61

  • 1Perou C M Pemu CM, Sorlie T, Eisen MB, et al. Molecular portrait of human breast, tumors [ J ]. Nature, 2012 (406) : 747 - 752.
  • 2Nielsen TO, Hsu FD, Jensen K, et al. Immunohistochemi- cal and clnicalcharacterization of the basal like subtype of iii vasive breast carcinoma [ J ]. Clin Cancer Res, 2011 (10) :5367 -5374.
  • 3Carey LA, Perou CM, Livasy CA, et al. Race, breast cancer subtypes,and survical in the Carolina breast cancer study [J]. JAMA, 2006(21) :2492 -2502.
  • 4Jarvinen TA, Tanner M, Rantanen V, et al. Amplification and deletion of topoisomerase II alphah associate with ErB2 amplification and affect sensitivity to topoisomerase II alphah inhibitor dosorubicin doxorubicin in breast canc- er [J]. Am J Pathol, 2010(3) :839 -847.
  • 5Sorile T, Perou CM,Tibshirani R, et al. Gene expression patterns of breast carcinomas distinguish tumor sumor sub- classes with clinical implications [ J ]. Proc Nat Acad Sci USA, 2010 (69) : 10869 - 10874.
  • 6Nielsen TO,Hsn FD,Jensen K, et al. Immnnohistochemi- cal and clnicalcharacterization of the basal like subtype of iii vasive breast carcinoma [ J 1. Clin Cancer Res, 2004 (10) :5367 - 5374.
  • 7Bauer K R, Brown M, CressR D, et al. Descriptive analysis of estrogen receptor (ER) Negative ,progesterone receptor (PR) negative,and HER-2 negative invasive breast canc- er, the socalled triple negative phenotype: a population based study from the California cancer Regaistry [ J 1. Cancer, 2007 (109) : 1721 - 1728.
  • 8Sng JH, Heaton VJ, Bell M, et al. Molecular cloning and characterization of the human topoisomerase II alpha and I/beta genes : Evidence for isoform evolution through gene duplication[ J]. Biochim Biophys Acta, 2009(1444) :395 - 406.
  • 9Menna P, Paz OG, Chello M, et al. Anthracycline cardiotoxicity[J]. Expert Opin Drug Saf, 2012,11( Suppl 1):S21-S36.
  • 10Bartlett JM, Mcconkey CC, Munro AF, et al. Predicting anthracycline benefit: TOP2A and CEP17-Not only but also[J]. J Clin Oncol, 2015,33(15):1680-1687.

引证文献4

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部