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FAK-原发性肝癌分子靶向治疗的新希望

FAK-New hope for molecular targeted therapies in primary hepatic carcinoma
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摘要 粘着斑激酶(focal adhesion kinase,FAK)是位于胞浆的一种非受体型酪氨酸激酶,它的功能包括调节细胞生长发育、存活和凋亡,以及调节细胞与细胞外基质黏附、细胞骨架重组等。FAK的高表达与多种肿瘤的发生发展、侵袭和转移有关。与正常肝组织和肝硬化组织相比,FAK的mRNA及蛋白水平在肝癌组织中呈过度表达或过度激活状态。FAK与肝癌细胞的增殖、凋亡、黏附、侵袭和转移密切相关,可望成为原发性肝癌分子靶向治疗的一个新希望。 Focal adhesion kinase (FAK) is cytoplasmic non-receptor type protein tyrosine kinase, the functions of FAK include regulating the growth and development, survival, apoptosis of cells, as well as regulating cell adhesion to extracellular matrix, recombination of cytoskeleton. Overexpression of FAK is concerned with the develop- ment, invasion, metastasis of many tumors. In contrast to normal liver and liver cirrhosis tissues, FAK mRNA and protein levels are overexpressed or overactived in liver cancer tissues. FAK is implicated in proliferation, apoptosis, adhesion, invasion, metastasis of hepatoma carcinoma ceils, it is conceivable that it would be another new hope for targeted therapies in primary hepatic carcinoma.
作者 陈川 王阁
出处 《现代肿瘤医学》 CAS 2008年第5期841-844,共4页 Journal of Modern Oncology
基金 国家自然科学基金资助项目(编号:30370341 30570410) 全国优秀博士专项基金资助项目(编号:200261)
关键词 粘着斑激酶 肿瘤 原发性肝癌 靶向治疗 focal adhesion kinase tumor primary hepatic carcinoma targeted therapy
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参考文献31

  • 1Thomas MB, Abbrtruzese JL. Opportunities for targeted therapies in hepatocellular carcinoma[ J ]. J Clin Oncol, 2005,23 (31 ) : 8093 - 8108.
  • 2Dunty JM, Schaller MD. The N termini of focal adhesion kinase family members regulate substrate phosphorylation, localization, and cell morphology[ J ]. J Biol Chem, 2002,277 (47) :45644 - 45654.
  • 3Sieg DJ, Hauck CR, Ilic D, et al. FAK integrates growth factor and integrin signals to promote cell migration[ J]. Nat Cell Biol, 2000,2(5 ) :249 - 256.
  • 4Taylor JM, Mack CP, Nolan K, et al. Selective expression of an endogenous inhibitor of FAK regulates proliferation and migration of vascular smooth muscle cells[J]. Mol Cell Biol, 2001,21 (5) : 1565 - 1572.
  • 5Brunton VG, Avizienyte E, Fincham V J, et al. Identification of Src - specific phosphorylation site on focal adhesion kinase: dissection of the role of Src SH2 and catalytic functions and their consequences for tumor cell behavior [ J ]. Cancer Res, 2005,65 (4) : 1335 - 1342.
  • 6Gelman IH. Pyk 2 FAKs, any two FAKs[J]. Cell Biol Int,2003, 27(7) :507 -510.
  • 7Miyazaki 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.
  • 8Schmitz K J, Grabellus F, Callies R, et al. High expression of focal adhesion kinase (p125FAK) in node - negative breast cancer is related to overexpression of HER -2/neu and activated Akt kinase but does not predict outcome [ J ]. Breast Cancer Res, 2005, 7 (2) :194 -203.
  • 9Han EK, Mcgonigal T, Wang J, et al . Functional analysis of focal adhesion kinase (FAK) reduction by small inhibitory RNAs[ J]. Anticancer Res, 2004 ,24(6 ) :3899 -3905.
  • 10Lark AL, Livasy CA, Calvo B, et al. Overexpression of focal adhesion kinase in primary colorectal carcinomas and colorectal liver metastases[J]. Clin Cancer Res ,2003, 9(1) : 215 -222.

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