期刊文献+

大肠癌中FAK的表达与生物学行为关系的研究 被引量:2

Expression of Focal Adhesion Kinase in Colorectal Carcinomas and its Biological Significance
下载PDF
导出
摘要 目的:研究粘着斑激酶(FAK)在大肠癌及癌旁组织中的表达及与肿瘤细胞分化、浸润、转移等生物学行为的关系。方法:应用免疫组织化学LSAB法检测60例大肠癌及癌旁组织石蜡标本中FAK蛋白的表达水平。结果:FAK在癌组织中的表达明显高于癌旁组织,低分化癌组织较高分化、中分化组织中FAK的表达高,有淋巴结转移的组织较无转移的组织表达高,浸润程度越深表达越高。结论:FAK可能是一种转化相关酶又是一种演变相关酶。FAK的表达量可作为肿瘤发生、发展过程中一种较有价值的病理指标。 Objective:To study the correlation between FAK expression in colorectal car-cinoma and noncancerous tissue and clinicopathological data including tumor differentiation,infil-trating and lymph node metastasis.Methods:Expression of FAK was examined in60colorectal carcinomas by immunohistochemical technique.Results:The staining of FAK was stronger in col-orectal carcinomas than in the epithelias of noncancerous areas and was higher in low differentia-tion cancer cells than in well differentiation ones.The cancers with lymph node metastasis had more FAK expression than the cancers without lymph node metastasis and the deeper extent of infiltrating,the higher FAK expression.Conclusions:The FAK might be not only a transformation related enzyme but also a progression related enzyme.The level of FAK expression might be a valuable marker for the carcinogenesis and progression of the carcinoma.
出处 《中国肿瘤临床》 CAS CSCD 北大核心 2003年第9期624-626,共3页 Chinese Journal of Clinical Oncology
基金 国家自然科学基金资助(编号:30170423)
关键词 大肠癌 免疫组织化学 粘着斑激酶 Colorectal carcinoma Immunohistochemistry Focal adhesion kinase
  • 相关文献

参考文献2

二级参考文献5

共引文献1368

同被引文献19

  • 1许良中,杨文涛.免疫组织化学反应结果的判断标准[J].中国癌症杂志,1996,6(4):229-231. 被引量:1365
  • 2Clark EA, Hynes RO.1997 Keystone symposiumon signal transduction by cell adhesion receptors [J]. BiochemBiophysActa, 1998,1 333(3):9 16.
  • 3Schlaepfer MD, Jones KC ,Hunter T. Multiple Grb2 mediated intergrin stimulated signaling pathways to ERK2 mitogen activated proteinkinase: summation of both Src and focaladhesionkinase initiated by rosinephosphorylation events [J]. MolCellBio1,1998,(5):2 571.
  • 4Schlaepfer MD, Parsons JT. Focal adhesion kinase and associated proteins [J]. CurrOpinCellBiol, 1994,6(5):705.
  • 5Ktay MH, Oktay K, Hamele-Bena D,et al. Focal adhesion kinase as a marker of malignant phenotype in breast and cervical carcinomas[J]. Hum Pathol, 2003, 34(3):240.
  • 6Schlaeofer DD , Jones KC , Hunter T. Multiplt Grb 2-mediated integrin stimulated signaling pathways to ERK 2 / mitogen-activated protein kinase: summation of both c-Src and focal adhesion kinase-initiated tyronsine phosphorylation events [ J ]. Mol Cell Biol,1998 (5) :2571-2585.
  • 7Oktay M, Wary KK, Dans M, et al. Integrin mediated activation of focal adhesion kinade is required for signaling to JunNH2-terminal kinase and progression through the Gphase of the cell cycle [ J ]. J cell Biol, 1999, 145: 1461-1469.
  • 8Calalb M , Pilte TR , Hanks SK. Tyrosinephosphorylation of focal adhesion kinase at sites in the catalytic domain regulates kinase activity: AroleforSrcfamily kinases [ J ]. Mol Cell Biol,1995, 15(2) :954-963.
  • 9Miyazaki T, Kato H , Nakajima M , et al. FAK overexpression is correlated with tumour invasiveness and lymph node metastasis in oesophageal squamous cell carcinoma [ J ]. Br J Cancer,2003,89(1) :140-145.
  • 10Schneider GB, Kurago Z, Zaharias R, et al. Elevated focal adhesion kinase expression facilitates oral tumor cell invasion.[J]Cancer,2002,95(12) :2508-2515.

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