期刊文献+

PTEN、p53和EGFR在乳腺癌中的表达与临床意义 被引量:12

Expression and clinical significance of PTEN,p53 and EGFR in breast carcinoma
下载PDF
导出
摘要 目的:检测PTEN、p53和EGFR在乳腺癌中的表达,分析它们与乳腺癌临床病理特征的关系及三者的相关性,并探讨其与乳腺癌预后的关系。方法:采用免疫组织化学SP法,检测PTEN、p53和EGFR在68例乳腺浸润性癌和10例乳腺纤维腺瘤组织标本中的表达。结果:PTEN、p53和EGFR在乳腺癌组织中的阳性率为45.6%、51.5%和58.8%,PTEN在乳腺癌组织中的表达明显低于纤维腺瘤组织,p53和EGFR在乳腺癌组织中的表达明显高于纤维腺瘤组织,差异有统计学意义(P<0.05)。PTEN、p53和EGFR蛋白在乳腺癌中表达与组织学分级、淋巴结转移情况、雌激素受体(ER)状态均有关(P<0.05)。PTEN和p53阳性率在死亡组与生存组的差异有统计学意义(P<0.05);EGFR阳性率在死亡组中高于生存组,但差异无统计学意义(P>0.05)。结论:PTEN表达的缺失和p53、EGFR的过度表达共同参与了乳腺癌的转移和进展,它们与肿瘤的侵袭性和预后有关。三者联合检测有助于乳腺癌的早期病理诊断、恶性程度的判断及预后的评估。 Objective:To evaluate the significance of PTEN,p53 and EGFR in the invasive breast cancer and the relationship between these markers and clinieopathologic parameter as well as clinical outcome. Methods: SP immunohistochemistry was used in detecting the expression of PTEN,p53 and EGFR in 68 eases of breast carcinoma and 10 eases of breast fibroadenoma. Results:The positive expression rate of PTEN, p53 and EGFR protein in breast carcinoma were 45.6% ,51.5% and 58.8% respectively,which were significantly different than that in breast fibroadenoma (P 〈 0.05). The expression of PTEN, p53 and EGFR in breast cancer was correlated with histological grade,lymph node metastasis and the status of ER(P 〈 0.05). The positive expression rate of PTEN in the death group was lower than that in the s urviwl group,which had statistically significant difference (P 〈 0.05 ) ; the positive expression rate of p53 (P 〈 0.05) and EGFR(P 〉 0.05) in the death group is significantly higher than that in the survival group. Conclusion:The deletion of PTEN as well as up - regulated expression of p53 and EGFR are involved in progression and invasion of breast carcinoma and indicate poor prognosis. The combined detection of these three markers could indicate early pathological diagnosis and prognosis of breast carcinoma.
出处 《现代肿瘤医学》 CAS 2014年第2期345-349,共5页 Journal of Modern Oncology
关键词 乳腺癌 免疫组化 PTEN P53 EGFR breast carcinoma immunohistochemistry PTEN p53 EGFR
  • 相关文献

参考文献19

  • 1Kurose K,Gilley K,Matsumoto S. Frequent somatic mutations in PTEN and Tp53 are mutually exclusive in the stroma of breast carcinomas[J].{H}Nature genetics,2002,(03):355-357.
  • 2Vitolo MI,Weiss MB,Szmacinski M. Deletion of PTEN promotes tumorigenic signaling,resistance to anoikis,and altered response to chemotherapeutic agents in human mammary epithelial cells[J].{H}CANCER RESEARCH,2009,(21):8275-8283.
  • 3Stambolic V,Tsao MS,Macpherson D. High incidence of breast and endometrial neoplasia resembling human Cowden syndrome in PTEN +/-mice[J].{H}CANCER RESEARCH,2000,(13):3605-3611.
  • 4Van Dyke T. p53 and tumor suppression[J].{H}New England Journal of Medicine,2007,(01):79-81.
  • 5Sotiriou C,Powles TJ,Dowsett M. Gene expression profiles derived from fine needle aspiration correlate with response to systemic chemotherapy in breast cancer[J].{H}Breast Cancer Research,2002,(03):R3.
  • 6Lialiaris TS,Kouskoakis A,Georgiou G. Expression of 6 common antigenic markers in invasive ductal breast carcinoma:potential clinical implications[J].{H}Applied Immunohistochemistry and Molecular Morphology,2011,(02):106-111.
  • 7Alsner J,Jensen V,Kyndi M. A comparison between p53 accumulation determined by immunohistochemistry and Tp53 mutations as prognostic variables in tumours from breast cancer patients[J].{H}ACTA ONCOLOGICA,2008,(04):600-607.
  • 8K Park,S Han B,E Shin. EGFR gene and protein expression in breast cancers[J].J Cancer Surg,2007,(33):956-960.
  • 9Matkovic B,Juretic A,Separovic V. Immunohistochemical analysis of ER,PR,HER-2,CK5/6,p63 and EGFR antigen expression in medullary breast cancer[J].{H}TUMORI,2008,(06):838-844.
  • 10赵荫农,何妮,欧超,曹骥,刘剑勇,袁卫平,吴飞翔,黄山.乳腺良、恶性病变中EGFR、EGFRvⅢ的表达及其临床意义[J].广西医科大学学报,2008,25(1):13-16. 被引量:2

二级参考文献8

  • 1欧超,吴飞翔,罗元,曹骥,赵荫农,袁卫平,李瑗,苏建家.表皮生长因子受体Ⅲ型突变体在肝细胞癌中的表达及意义[J].癌症,2005,24(2):166-169. 被引量:19
  • 2Arteaga CL. Epidermal growth factor receptor dependence in human tumors: more than just expression. On cologist.2002,7(Suppl 1) :31-39.
  • 3Yaden Y. Sliwkowski MX. Untangling the ErbB signa ling net work[J]. Nat Rev Mol all Biol.2001,2(2):127-137.
  • 4KlapperLN, Kirschbaum MA,Sela M,et al. Biochemical and clinical implications of the ErbB/HER signaling network of growth facter receptors[J]. Adv Cancer Res,2000,77:25-79.
  • 5Wikstrand CJ, Reist CJ, Archer GE, et al. The Class Ⅲ variant of epidermal growth factor receptor (EGFRv Ⅲ): Charaterization and utilization as immunotherapeutie target[J]. J Neuroviro, 1998,4(2) : 118-158.
  • 6Pedersen MW,Meltorn M,DamstrllP L,et al. The type Ⅲ epidermal growth factor receptor mutation, biological. Significant and potential target for anti-cancer therapy[J]. Ann Oncol,2001,12(6):745-760.
  • 7Moscatello DK, Holgado-Madruga M. Godwin AK, et al. Frequent expression of a mutant epidermal growth factor receptor in multiple human tumors [J]. Cancer Res,1995,55(23):5 536-5 539.
  • 8Damstrup L, Wandahl RM. Basthoiml, et al. Epidermal growth factor receptor mutation type transfected into a small sell lung cancer cell line is predominantly localized at the cell surface and enhances the malignant phenotype[J]. Int J Cancer,2002,97(1):7-11.

共引文献1

同被引文献112

  • 1耿进朝,周玉荣,刘晋红,翁艳,李明山,刘晶哲.乳腺癌的ER、PR、C-erbB-2和P53表达与钼靶X线表现相关性研究[J].中华放射医学与防护杂志,2006,26(5):486-489. 被引量:32
  • 2中国癌症防治办公室,中国抗癌协会.中国常见恶性肿瘤诊治规范[M].北京:北京医科大学、中国协和医科大学联合出版社,1990:10.
  • 3吴绍新,王涛,付颖,官德元.E-cd及CD_(44)V_6在乳腺癌中的表达及意义[J].右江民族医学院学报,2007,29(6):969-970. 被引量:1
  • 4蒙彦军.乳腺癌发病现况的研究进展[J].中国药物经济学,2013(3):440.441.
  • 5Chen KH,Guo X,Ma D,et al.Dysregulation of HSG triggers vascular proliferative disorders[J].Nat Cell Biol,2004,6(9):872-879.
  • 6Mitsudomi T,Yatabe Y.Epidermal growth factor receptor in relation to tumor development:EGFR gene and cancer[J].FEBS J,2010,277(2):301-306.
  • 7El-Rayes BF,LoRusso PM.Targeting the epidermal growth factor receptor[J].Br J Cancer,2004,91(3):418-422.
  • 8Wang W,Zhu F,Wang S,et al.HSG provides antitumor efficacy on hepatocellular carcinoma both in vitro and in vivo[J].Oncol Rep,2010,24(1):183-190.
  • 9Pich S,Bach D,Briones P,et al.The Charcot-Marie-Tooth type 2A gene product,Mfn2,up-regulates fuel oxidation through expression of OXPHOS system[J].Hum Mol Genet,2005,14(11):1405-1415.
  • 10Zhen Y,Guanghui L,Xiefu Z.Knockdown of EGFR inhibits growth and invasion of gastric cancer cells[J].Cancer Gene Ther,2014,21(11):491-497.

引证文献12

二级引证文献56

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