期刊文献+

CRABPⅡ和E-FABP在乳腺浸润性导管癌中的差异性表达及其意义 被引量:2

Expression of CRABPII and E-FABP in breast invasive ductal carcinoma and their significance
下载PDF
导出
摘要 目的探讨CRABPII和E-FABP在乳腺浸润性导管癌中的表达差异及与临床病理特征和预后的关系。方法采用免疫组化SP法检测152例乳腺浸润性导管癌中CRABPII和E-FABP的表达。结果 CRABPII和EFABP在乳腺浸润性导管癌中的表达存在差异(P<0.05),E-FABP 72.4%的阳性率高于CRABPII的33.6%。CRABPII和E-FABP的差异性表达与肿瘤有/无转移、TNM分期有关(P<0.05),与患者预后无关(P>0.05)。结论在乳腺浸润性导管癌中,E-FABP在肿瘤中的阳性表达率较CRABPII高,伴有癌转移、TNM分期晚的肿瘤阳性率更高。调节肿瘤细胞中CRABPII/E-FABP的比例有望成为乳腺癌个性化靶向治疗研究的新方向。 Objective To study the differential expression between CRABPII and E-FABP in breast invasion ductal carcinoma (IDC)and their clinical significance. Methods CRABPII and E-FABP proteins were detected in 152 cases of IDC by SP method of immunohistochemical staining. Results CRABPII and E-FABP showed different expression distribution in IDC (P 〈 O. 05 ). The expression level of E-FABP had a recognizable advantage over that of CRABPII. The differential expression between CRABPII and E-FABP was correlated to the metastasis and TNM staging, but not correlated to the prognosis of IDC patients (P 〉 0. 05 ). Conclusions The expression level of E-FABP has a recognizable advantage over that of CRABPII in IDC, the later the TNM staging is, along with cancer metastasis, the more likely the expression of E-FABP would dominate. Regulating the CRABPII/E-FABP ratio in tumor cells may be the new direction of research on target therapy of breast carcinoma.
出处 《诊断病理学杂志》 CSCD 北大核心 2013年第10期638-641,共4页 Chinese Journal of Diagnostic Pathology
基金 四川省卫生厅科研资助课题(100174)
关键词 乳腺肿瘤 浸润性导管癌 CRABPII E-FABP 预后 免疫组化 Breast neoplasms Invasive ductal carcinoma CRABPII E-FABP Prognosis Immunohistochemistry
  • 相关文献

参考文献11

  • 1Schug 33', Berry DC, Shaw NS, et al. Opposing effects of retinoic acid on cell growth result from alternate activation of two different nuclear receptors [ J ]. Cell, 2007,129 (4) :723 - 733. 被引量:1
  • 2Zimmerman AW, van Moerkerk HTB, Veerkamp JH. Ligand specificity and conformational stability of human fatty acid- binding proteins[ J]. Int J Bioehem Cell Biol, 2001,33 (9) :865 - 876. 被引量:1
  • 3Rochette-Egly C, Chambon P. 10 embryocarcinoma ceils : a cell autonomous model to study the functional selectivity of RARs and RXRs in retinoid signaling [ J]. Histol Histopathol, 2001,16 (3) :909 -922. 被引量:1
  • 4Donato LJ, Suh JH, Noy N. Suppression of mammary carcinoma cell gro.h hy retinoic acid: the cell cycle control gene Btg2 is a direct target for retinoic acid receptor signaling [ J ]. Cancer Res, 2007,67(2) :609-615. 被引量:1
  • 5Oonato LJ, Noy N. Suppression of mammary carcinoma growth by retinoic acid: Proapoptotic genes are targets for retinoic acid receptor and cellular retinoic acid-binding protein II signaling [ J 1. Cancer Res, 2005,65 ( 18 ) : 8193 - 8199. 被引量:1
  • 6Di-Pi N, Tan NS, Michalik L, et al. Antiapoptotic role of PPAR beta in keratinocytes via transcriptional control of the Aktl signaling pathway [ J ]. Mol Cell, 2002,10 (4) :721 - 733. 被引量:1
  • 7Shaw N, Elholm M, Noy N. Retinoic acid is a high affinity selective ligand for the pemxisome proliferator-activated receptor 13/8[ J]. J Biol Chem, 2003,278(43) :41589 -41592. 被引量:1
  • 8Garattini E, Gianni M, Terao M. Retinoids as differentiating agents in oncology: a network of interactions with intracellular pathways as the basis for rational therapeutic combinations [ J ]. Curt Pharm Des, 2007,13(13) :1375 -1400. 被引量:1
  • 9Schug TY, Berry DC, Toshkov IA, et al. Overcoming retinoic acid-resistance of mammary carcinomas by diverting retinoic acid from PPAR beta/delta to RAR [ J ]. Proc Natl Acad Sci U S A, 2008,105 (21) :7546 -7551. 被引量:1
  • 10Budhu AS, Noy N. Direct channeling of retinoic acid between cellular retinoic acid-binding protein II and retinoic acid receptor sensitizes mammary carcinoma ceils to retinoic acid-induced growth arrest[ J]. Mol Cell Biol, 2002,22 ( 8 ) :2632 - 2641. 被引量:1

同被引文献20

引证文献2

二级引证文献2

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