Department of Genitourinary Medical Oncology, University of Texas M D Anderson Cancer Center, Houston, TX 77030-4009, USA.
Mol Cancer Res. 2009 Nov;7(11):1781-91. doi: 10.1158/1541-7786.MCR-09-0255. Epub 2009 Nov 10.
Caveolin-1 (cav-1) and the cancer-promoting growth factors vascular endothelial growth factor (VEGF), transforming growth factor beta1 (TGF-beta1), and fibroblast growth factor 2 (FGF2) are often found to be upregulated in advanced prostate cancer and other malignancies. However, the relationship between cav-1 overexpression and growth factor upregulation remains unclear. This report presents, to our knowledge, the first evidence that in prostate cancer cells, a positive autoregulatory feedback loop is established in which VEGF, TGF-beta1, and FGF2 upregulate cav-1, and cav-1 expression, in turn, leads to increased levels of VEGF, TGF-beta1, and FGF2 mRNA and protein, resulting in enhanced invasive activities of prostate cancer cells, i.e., migration and motility. Our results further show that cav-1-enhanced mRNA stability is a major mechanism underlying the upregulation of these cancer-promoting growth factors, and that PI3-K-Akt signaling is required for forming this positive autoregulatory feedback loop.
窖蛋白-1(cav-1)和促进肿瘤生长的血管内皮生长因子(VEGF)、转化生长因子β1(TGF-β1)和成纤维细胞生长因子 2(FGF2)在晚期前列腺癌和其他恶性肿瘤中常被发现过度表达。然而,cav-1 过表达与生长因子上调之间的关系尚不清楚。本报告首次提出了在前列腺癌细胞中建立正反馈环的证据,即 VEGF、TGF-β1 和 FGF2 上调 cav-1,而 cav-1 表达又导致 VEGF、TGF-β1 和 FGF2 mRNA 和蛋白水平升高,从而增强了前列腺癌细胞的侵袭活性,即迁移和运动。我们的研究结果还表明,cav-1 增强的 mRNA 稳定性是上调这些促进癌症生长的生长因子的主要机制,而 PI3-K-Akt 信号通路是形成这种正反馈环所必需的。