期刊文献+

乳腺浸润性导管癌组织FGFR1与AIB1表达及其相关性研究 被引量:1

Expression and correlation of FGFR1 and AIB1 in invasive ductal carcinoma of breast
原文传递
导出
摘要 目的:探讨乳腺浸润性导管癌(invasive ductal carcinoma,IDc)中成纤维细胞生长因子受体1(fibroblast growth factor receptor1,FGFRl)和乳腺癌扩增性抗原1(amplified in breast cancer 1,AIBl)的表达,分析两者与乳腺IDC临床特征的关系以及两者的相关性。方法:采用免疫组织化学SP法检测2006—01-01—2011-06-30河北省人民医院100例经病理科医师确诊、临床病例资料完整的乳腺IDC组织石蜡标本中FGFRl及AIBl的表达情况,分析两者与临床病理特征的关系及两者的相关性。统计所有数据均采用SPSS17.0统计软件进行分析,采用Y。检验或Fisher确切概率法对同一指标的不同临床病理特征进行比较,应用多因素Logistic回归分析FGFRl及AIBl阳性表达有关的因素,采用Spearman等级相关分析乳腺IDC中FGFRl和AIBl表达的相互关系。结果:FGFRl在乳腺IDC中的阳性表达率为31.oo%,其表达与腋窝淋巴结转移(42.86%珊22.41%)、病理组织学分级(Ⅰ级0,Ⅱ级26.80%,Ⅲ级51.60%)和临床分期(Ⅰ期11.10%,Ⅱ期29.40%,Ⅲ期65.00%)有关,差异均有统计学意义,X^2值分别为4.760、12.463和15.671,P值分别为0.029、0.002和〈0.001;AIBl在乳腺IDC中的阳性表达率为75.00%,与腋窝淋巴结转移与否(83.33%79S68.97%)有关,差异有统计学意义(X^2=4.433,P-0.035),其表达随着病理组织学分级(Ⅰ级38.46%,Ⅱ级75.0。%,Ⅲ级90.32%)和临床分期(Ⅰ期44.44%,Ⅱ期84.31%,Ⅲ~Ⅳ期95.OO%)的增高而逐渐增高,差异均有统计学意义(X^2=13.138,P-0.001;x。=20.336,P〈0.001);多因素Logistic回归分析显示,组织学分级是影响FGFRl及AIBl阳性表达的最主要因素(wald X^2=13.448,P=0.003;wald X^2=7.958,P一0.001)。FGFRl与AIBl表达在乳腺IDC中呈正相关,r-0.237,P-0.017。结论:FGFRl及AIBl与乳腺IDC的淋巴结转移、病理组织学分级及临床分期有关,提示两者与乳腺IDC的发生和发展密切相关,且两者表达呈正相关,联合检测两者可能对乳腺ID2的预后判断更有价值。 OBJECTIVE: To investigate the correlation between the protein expressions of fibroblast growth factor receptorl(FGFR1) and amplified in breast cancer 1 (AIB1) in invasive ductal carcinoma (IDC) of breast and the associa- tions with clinical features. METHODS: S-P Immunohistochemical techniques were adopted to detect the expression of FGFR1 and AIB1 in 100 cases of IDC who were collected from 2006-01-01 to 2011-06-30 in Hebei General Hospital, and had been confirmed by histopathology, with the complete clinical data. SPSS 17.0 statistical software was used for statis- tical analysis. X2 test or Fisher exact Test was used to compare different clinical pathological features of the same parame- ter. Logistic regression analysis was applied for the analysis of positive expression-related factors of FGFR1 and AIB1. Spearman rank correlation was used to analyse the interrelation of FGFR1 and AIB1 in IDC. RESULTS: The positive ex- pression rate of FGFR1 in IDC tissues was 31.00%. The expression of FGFR1 was positively related to the lymph node metastasis(42.86% vs 22.41%), histological grade( Ⅰ grade 0, Ⅱ grade 26.80%, Ⅲ grade 51.60%), clinical stage(Ⅰ staging 11.10 %, Ⅱ staging 29.40 %, Ⅲ-- IV staging 65.00 % ), with statistical significance (X^2 = 4. 760, P = 0. 029 ; Xz = 12. 463, P= 0. 002; X2= 15. 671, P〈0. 001, respectively). The positive expression rate of AIB1 in IDC tissues was 75.00%. The positive expression rate of AIB1 in lymph node positive group was significantly higher than that in lymph node negetive group (83.33 % vs 68.970, X^2 = 4. 433, P = 0. 035), and increased along with the histologic grading ( Ⅰ grade 38.46 %, Ⅱ grade 75.00 %, Ⅲ grade 90.32 % ) and clinical stage( Ⅰ staging 44.44 %, Ⅱ staging 84.31%, Ⅲ -- Ⅳ stag- ing 95.00%), the positive expression rate of FGFR1 increased gradually, and the difference was statistically significant (X^2 = 13. 138, P= 0. 001 ; z = 20. 336, P〈0. 001, respectively). Logistic regression analysis showed that the histological grade of IDC was the main factor impacting the expression of FGFR1 and AIB1 (wald X^2 = 13. 448, P=0. 003; wald .X^2 = 7. 958, P=0. 001). FGFR1 expression had a positive correlation with the expression of AIB1 (r=0. 237,P=0. 017). CONCLUSIONS: The expression of FGFR1 and AIB1 have close correlation with lymph node metastasis, histological grade, clinical stage,which present that both proteins have relationship with ocurrance and progress of IDC. FGFR1 is positively related to AIB1 in IDC,and combined detection of them may be valuable for evaluating the prognosis of IDC.
出处 《中华肿瘤防治杂志》 CAS 北大核心 2014年第8期594-598,共5页 Chinese Journal of Cancer Prevention and Treatment
基金 河北省科技支撑计划(11276103D-70)
关键词 乳腺肿瘤 浸润性导管癌 FGFR1 AIB1 免疫组织化学 预后 breast neoplasms invasive ductal carcinoma fibroblast growth factor receptorl amplified in breast canc-er 1 immunohistochemistry prognosis
  • 相关文献

参考文献18

  • 1Turner N,Pearson A,Sharpe Rvet al. FGFR1 amplification drives en-docrine therapy resistance and is a therapeutic target in breast cancer [J]. Cancer Res,2010, 70(5) :2085-2094.
  • 2Weiss J .Sos ML,Seidel D, et al. Frequent and focal FGFR1 am-plification associates with therapeutically tractable FGFR1 de-pendency in squamous cell lung cancer[J]. Sci Transl Med , 2010, 2(62) :62-93.
  • 3Tsimafeyeu I, Demidov L, Stepanova E, et al. Overexpression of fibroblast growth factor receptors FGFR1 and FGFR2 in renal cell carcinoma[J]. Scand J Urol Nephrol,2011,45(3) :190-195.
  • 4Elbauomy Elsheikh S, Green AR, Lambros MB, et al. FGFR1 amplification in breast carcinomas: a chromogenic in situ hybridi-sation analysis[J]. Breast Cancer Res, 2007 ,9(2) : 23.
  • 5Tenhagen M, van Diest PJ, Ivanova lA, et al. Fibroblast growth factor receptors in breast cancer: expression, downstream effects, and possible drug targets [J]. Endocr Relat Cancer, 2012,19(4):115-129.
  • 6Jang MH, Kim EJ .Choi v, et al. FGFR1 is amplified during the progression of in situ to invasive breast carcinoma [J]. Breast Cancer Res,2012,14(4) :115-127.
  • 7李庆霞,张炎,王娟,张明,潘海燕,苗军程.成纤维细胞生长因子受体1在乳腺癌中的表达及意义[J].中华实验外科杂志,2012,29(5):814-814. 被引量:3
  • 8张君红,林瑶光.胃癌组织Flt-1和PDGFR及bFGFR表达与MVD相关性研究[J].中华肿瘤防治杂志,2013,20(4):269-272. 被引量:8
  • 9刘春忻.bFGF、FGFR1和FGFR2在子宫内膜癌的表达和临床意义[J].中国实验诊断学,2011,15(8):1331-1334. 被引量:4
  • 10Spears M,Oesterreich Sv Migliaccio I.et al. The p160 ER co-reg-ulators predict outcome in ER negative breast cancer[J]. Breast Cancer Res Treat,2012,131(2): 463-472.

二级参考文献47

  • 1许会彬,张代民,曹英林.碱性成纤维细胞生长因子及受体与肿瘤的关系[J].临床军医杂志,2005,33(1):98-100. 被引量:18
  • 2徐迎春,林玉梅,张凤春.乳腺癌内分泌治疗耐药机制研究进展[J].中华肿瘤防治杂志,2006,13(3):227-231. 被引量:8
  • 3林瑶光,韦良宏.大肠癌COX-2和BFGFR表达与Dukes分期,淋巴结转移之间的关系[J].陕西医学杂志,2007,36(3):293-295. 被引量:3
  • 4Osborne CK, Bardou V, Hopp TA, et al. Role of the estro gen receptor coaetivator AIB1 (SRG3) and HER-2/neu in Tamoxifen resistance in breast cancer[J]. Journal of the National Cancer Institute, 2003, 95(5):353-361.
  • 5Bouras T, Southey MC, Venter DJ. Overexpression of the steroid receptor coactivator AIB-1 in breast cancer correlates with the absence of estrogen and progesterone receptors and positivity for p53 and HER-2/neu[J]. Cancer research, 2001, 61(3) :903- 907.
  • 6Henke RT, Haddad BR, Kim SE, et al. Overexpression of the nuclear receptor coactiator AIB1 (SRC 3) during progression of pancreatic adenocarcinoma[J].Clin Cancer Res, 2004,10(18pt1): 6134-6142.
  • 7Anzick SL, Kononen J, Walker RL, et al. AIB1, a steroid receptor coactivator amplified in breast and ovarian cancer[J].Science, 1997, 277(5328): 965-968.
  • 8Shao W, Keeton EK, McDonnell DP, et al. Coactivator AIB1 links estrogen receptor transcriptional activity and stability [J]. PNAS, 2004, 101(32):11599-11604.
  • 9Auboeuf D, Honig A, Berget SM,et al. Coordinate regulation of transcription and splicing by steroid receptor coregulators [J]. Science, 2002, 298(5592):416- 419.
  • 10Zhou G, Hashimoto Y, Nwak I, et al. Role of the steroid receptor coactivator SRC- 3 in cell growth[J]. Mol Cell Biol, 2003, 23(21) :7742-7755.

共引文献17

同被引文献1

引证文献1

二级引证文献1

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