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ERK/MAPK信号传导途径在乳腺肿瘤治疗中的意义 被引量:15

Role of ERK/MAPK pathway in treatment of breast tumors
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摘要 ERK/MAPK途径在乳腺癌的发生和发展中起着重要的作用,该通路有3个关键靶分子:小G蛋白Ras及其下游的Raf激酶、MEK1/2和ERK1/2。ERK/MAPK信号转导途径的激活将促进乳腺肿瘤细胞的增殖,因此阻断该信号转导途径就可以干预肿瘤的进程,这为乳腺癌的治疗提供了一种新的策略。目前主要有3种抑制ERK/MAPK信号转导途径的方法:(1)利用抑制剂破坏主要靶蛋白的结构和功能;(2)抑制靶蛋白之间的相互作用,阻止信号转导;(3)利用反义核苷酸技术使靶分子功能缺失从而阻断级联反应。这些方法为乳腺肿瘤的治疗提供了新的思路,相信它们将对乳腺肿瘤的治疗做出重要的贡献。
作者 张丰 李楠
出处 《中国肿瘤生物治疗杂志》 CAS CSCD 2007年第5期497-500,共4页 Chinese Journal of Cancer Biotherapy
基金 国家自然科学基金(No.30570370) Surpported by the National Natural Science Foundation of China(No.30570370)
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  • 1Adeyinka A, Nui Y, Cherlet T, et al. Aetivated mitogen-activated protein kinase expression during human breast tumorigenesis and breast cancer progression [ J ]. Clin Cancer Res, 2002, 8 (6) :1747-1753.
  • 2Spencer KS, Graus-Porta D, Leng J, et al. ErbB2 is necessary for induction of carcinoma cell invasion by ErbB family receptor tyrosine kinases[J]. J Cell Biol, 2000. 148(2) : 385-397.
  • 3Lee TJ, Lee JT, Park JW, et al. Acquired TRAIL resistance in human breast cancer cells are caused by the sustained cFLIP(L) and XIAP protein levels and ERK activation [ J ]. Biochem Biophys Res Commun, 2006,351 (4) :1024-1030.
  • 4Johnston SR, Hickish T, Ellis P. et al. Phase Ⅱ study of the efficacy and tolerability of two dosing regimens of the farnesyl transferase inhibitor, R115777, in advanced breast cancer[ J ]. J Clin Oncol, 2003,21 ( 13 ) :2492-2499.
  • 5Kelland LR, Smith V, Valenti M, et al. Preclinical antitumor activity and pharmacodynamic studies with the farnesyl protein transferase inhibitor R115777 in human breast cancer[ J ]. Clin Cancer Res, 2001,7( 11 ) :3544-3550
  • 6End DW, Smets G, Todd AV, et al. Characterization of the antitumor effects of the selective farnesyl protein transferase inhibitor R115777 in vivo and in vitro [ J ]. Cancer Res, 2001,61 ( 1 ) : 131 - 137.
  • 7Lee M, Koh WS, Han SS. Down-regulation of Raf-1 kinase is associated with paclitaxel resistance in human breast cancer MCF-7/ Adr cells[ J]. Cancer Lett, 2003,193 ( 1 ) :57-64.
  • 8Lyons JF, Wilhelm S, Hibner B, et al. Discovery of a novel Raf kinase inhibitor[ J]. Endocr Relat Cancer, 2001, 8 ( 3 ) : 219- 225.
  • 9Ochel HJ, Eichhom K, Gademann G. Geldanamycin: the prototype of a class of antitumor drugs targeting the heat shock protein 90 family of molecular chaperones [ J ]. Cell Stress Chaperones, 2001,6 (2) : 105-112.
  • 10Beliakoff J, Bagatell R, Paine-Murrieta G, et al. Hormone-refractory breast cancer remains sensitive to the antitumor activity of heat shock protein 90 inhibitors[ J]. Clin Cancer Res, 2003,9 ( 13 ) : 4961-4971.

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