期刊文献+

乳腺癌中HER-2、P16和P53的表达及预后意义 被引量:7

乳腺癌中HER-2、P16和P53的表达及预后意义
下载PDF
导出
摘要 目的研究乳腺癌中HER-2、P16和P53蛋白表达及其对预后评估的意义。方法采用免疫组织化学法检测85例乳腺癌组织HER-2、P16和P53蛋白的表达。结果 (1)HER-2过表达阳性率为23.5%(20/85),P16和P53阳性的表达率分别为30.6%(26/85)和51.8%(44/85)。(2)HER-2与组织学分级相关(P<0.05);P16与年龄、ER、PR相关(P<0.05));P53与PR、P16相关(P<0.05)。(4)HER-2过表达阴性患者的无瘤生存率明显高于阳性患者,随着HER-2表达的增强,无瘤生存曲线下降(P<0.05),COX模型多因素生存分析结果显示,TNM分期,HER-2和P16是影响乳腺癌患者无瘤生存期的独立预后因素(P<0.05)。结论 HER-2、P16和P53与乳腺癌的发生发展密切相关,可作为指导治疗和估计预后的参考指标,特别是TNM分期,HER-2和P16是判断乳腺癌术后无瘤生存的独立有效指标。 Objective This study was to evaluate the prognostic significance of the expression of HER-2、P16 and p53 in patients with breast carcinoma.Methods HER-2、P16 and p53 protein levels in tumors from eighty five breast carcinoma patients were determined using immunohistochemistry analysis.Results (1)Of the 85 breast carcinoma, 20(23.5%)were found to be HER-2 over expression , 26(30.6%)were found to be P16 expression, and 44(51.8%)were found to be P53 expression.(2)There was significant correlation between the over expression of HER-2 and histological Grade(P〈0.05). P16 expression was correlated with age , ER and PR(P〈0.05). P53 expression was correlated with PR and P16 (P〈0.05).(4)The disease-free survival (DFS)rate was significantly higher in HER-2-negative group than in HER-2-positive group. The DFS curve had a tendency to decline with the stronger expression of HER-2.(P〈0.05). Cox's proportional hazards regression model revealed that HER-2 over expression, P16 expression, and TNM stage were independent prognostic factors of breast carcinoma (P〈0.05).Conclusion The gene products of HER-2, P16 and P53 play a significant role in the oncogenesis and development of cancer, and may be used as reference indicator to judge direction therapy and predict prognosis. HER-2 over expression, P16 expression and TNM stage are independent prognostic parameters for postoperative DFS in patients with breast carcinoma.
机构地区 广西医科大学
出处 《当代医学》 2011年第9期15-17,共3页 Contemporary Medicine
关键词 乳腺癌 HER-2 P16 P53 预后 Breast carcinoma:HER-2:P16:P53:Prognosis
  • 相关文献

参考文献15

  • 1Cooke T,Eeeves J,Lanigan A,et aI.HEP,2 as a prognostic and predictive marker for breast cancer[J].Ann 0ncol,200],12(1):25-28.
  • 2Kamil M,Yusuf N,Kh&lid I,et al.Associ&tion between HER-2/ neu over expression and clinico pathologic parameterg of breast cancer in northern Malaysia[J].Oeylon Med J,20]0,55(1):9 13.
  • 3Toikkanen S,Helin H,Isola J,et aI.Prognostic significance ofHER-2 oncoprotein expression in bre&st c&ncer:& 50--ye&r follow--up[J].JClin Oncol,1992, 1 0(7):1044-1048.
  • 4Strauss B Best hope or last hope: access to phase Ill clinicaltrials of HER-2/neu for advanced stage breast cancer patients[J].J AdvNurs,2000,51(2):259 266.
  • 5Borg A,andon A K,Sigurdsson H,et aI.HEE--2/neu ampiificationpredicts poor survival in node-posftive breast cancer[J].C&ncerEes.1990.50(14).4552-4557.
  • 6Ohtani N,Yamakoshi K,Takahashi A,et al.The pl61NK4a-RB pathway:molecular link between cellular senescence and tumor suppression[J]. J Med Invest,2004,51(5 4):146-155.
  • 7Tsuda H,Yamamoto K,Inoue T, et al.The role of pl6--cyclin d/ CPK--pRb pathway in the tumorigenesis of endometrioid type endornetrial carcinorna[J].Br J Cancer,2000,82(5):675-682.
  • 8Merlo A,Herman J O Mao L,et &l. 5' CpG island methyIation is associated with transcrfptionsl silencing of the tumour suppressor p16/ CDKN2/MTS1 in human cancers[J].Nat Med,1995,1(7):686-692.
  • 9Vousden K H,Lu X.Live or let die:the cellrs response to p55[J].Nat P.ev Cancer,2002,2(8):594-604.
  • 10Casey G,Lo-Hsueh M,Lopez M E,et al.Growth suppression ofhuman breast cancer cells by the introduction of a wild-type p53 gene[J]. Oncogene,1991,6( 0): 79 -797.

同被引文献101

  • 1廖健伟,邵佳佳,王鹏,蒋圆玲,萧晓琴,彭小芳,李晓娟,欧阳能太.乳腺癌分子分型与遗传基因变异谱关系的初步探讨[J].岭南急诊医学杂志,2020(5):499-503. 被引量:2
  • 2许少峰,付丽.p53研究的新进展[J].中华病理学杂志,2004,33(6):559-561. 被引量:24
  • 3郭树彬,杨红,陆星华,钱家鸣,刘军波,陈琳洁,王升启.胰腺癌抑癌基因P16、DPC4寡核苷酸芯片点突变及缺失的应用[J].临床内科杂志,2007,24(6):419-422. 被引量:2
  • 4Wentzensen N,sherman ME,Schiffman M,et a1.Utility of methylation markers in cervical cancer early detection:appraisal of the tate-of-thescience[J].Gynecol Oncol,2009,112(2):291-293.
  • 5Negri G,Bellisano G,Zannoni G F,et a1.P16ink4a and HPV L1 immunohistochemistry is helpful for estimating the behavior of lowgrade dysplastie lesions of the cervix uteri[J].Am J Surg Pathol,2008,32(11):1715-1720.
  • 6Badaracco G,Savarese A,Micheli A,et a1.Persistence of HPV after radio—chemotherapy in locally advanced cervicai cancer[J].Oncol Rep,2010,23(4):l093-1095.
  • 7Higgins MJ, Baselga J. Targeted therapies for breast cancer [ J]. J Clin Invest, 2011 , 121 (10) :3797-3803.
  • 8Gould VE, Martinez N, Orucevic A, et al. A novel, nuclear pore- associated, widely distributed molecule overexpressed in oncogenesis and development [ J ]. Am J Pathol, 2000,157 ( 5 ) : 1605-1613.
  • 9Wang-Rodriguez J, Dreilinger AD, Alsharabi GM, et al. The signa- ling adapter protein PINCH is up-regulated in the stroma of common cancers, notably at invasive edges [ J ]. Cancer, 2002,95 ( 6 ) : 1387-1395.
  • 10Gajria D, Chandarlapaty S. HER2-amplified breast cancer: mecha- nisms of trastuzumab resistance and novel targeted therapies [ J ]. Expert Rev Anticancer Ther, 2011,11 (2) :263-275.

引证文献7

二级引证文献17

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