Boyce Brendan, Xing Lianping
Department of Pathology & Laboratory Medicine, University of Rochester Medical Center, 601 Elmwood Avenue, Box 626, Rochester, NY 14642, USA.
Clin Investig (Lond). 2011 Dec 1;1(12):1695-1706. doi: 10.4155/cli.11.150.
Src is a nonreceptor tyrosine kinase essential for the activation of osteoclasts, the cells that degrade bone. Src also regulates normal cell functions, cancer cell growth and metastasis to organs, including bone where tumor cells induce bone destruction by osteoclasts. Src inhibitors prevent bone destruction and tumor cell growth in animal models of metastatic bone disease, and some are being investigated in clinical trials, particularly in patients with prostate cancer, which has high bone metastatic potential. Here, we review how Src regulates osteoclast formation, activation and survival and the results of preclinical and clinical trials of Src inhibitors, which show some promise in inhibiting the effects of tumor cells on the skeleton.
Src是一种非受体酪氨酸激酶,对于破骨细胞(即降解骨骼的细胞)的激活至关重要。Src还调节正常细胞功能、癌细胞生长以及向包括骨骼在内的器官转移,在骨骼中肿瘤细胞会通过破骨细胞诱导骨质破坏。Src抑制剂可预防转移性骨病动物模型中的骨质破坏和肿瘤细胞生长,一些抑制剂正在进行临床试验研究,特别是在具有高骨转移潜力的前列腺癌患者中。在此,我们综述Src如何调节破骨细胞的形成、激活和存活,以及Src抑制剂的临床前和临床试验结果,这些结果在抑制肿瘤细胞对骨骼的影响方面显示出一些前景。