Lee David, Gautschi Oliver
CIG Media Group, LP, Dallas, TX, USA.
Clin Lung Cancer. 2006 May;7(6):381-4. doi: 10.3816/clc.2006.n.020.
Src tyrosine kinases regulate a large number of important mechanisms in normal and cancerous cells, are overexpressed in a broad range of tumors including lung cancer, and thus represent a potential target for cancer therapy. Preclinical experiments indicate that small-molecule inhibitors of Src block tumor growth, metastasis, and angiogenesis. Phase I data from healthy volunteers also suggest that inhibitors of Src prevent bone resorption. Several phase II trials with small-molecule inhibitors of Src are under way or have been initiated in lung cancer and in other malignancies, as discussed herein.
Src酪氨酸激酶调节正常细胞和癌细胞中的大量重要机制,在包括肺癌在内的多种肿瘤中过度表达,因此是癌症治疗的一个潜在靶点。临床前实验表明,Src的小分子抑制剂可阻断肿瘤生长、转移和血管生成。来自健康志愿者的I期数据也表明,Src抑制剂可预防骨质吸收。如本文所讨论的,几项针对Src小分子抑制剂的II期试验正在肺癌和其他恶性肿瘤中进行或已经启动。