Endocrine Mechanisms and Hormone Action Program, Department of Urology, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
PLoS One. 2012;7(6):e40148. doi: 10.1371/journal.pone.0040148. Epub 2012 Jun 28.
The insulin-like growth factor receptor I (IGF-IR) plays an essential role in transformation by promoting cell growth and protecting cancer cells from apoptosis. We have recently demonstrated that the IGF-IR is overexpressed in invasive bladder cancer tissues and promotes motility and invasion of urothelial carcinoma cells. These effects require IGF-I-induced Akt- and MAPK-dependent activation of paxillin. The latter co-localizes with focal adhesion kinases (FAK) at dynamic focal adhesions and is critical for promoting motility of urothelial cancer cells. FAK and its homolog Proline-rich tyrosine kinase 2 (Pyk2) modulate paxillin activation; however, their role in regulating IGF-IR-dependent signaling and motility in bladder cancer has not been established. In this study we demonstrate that FAK was not required for IGF-IR-dependent signaling and motility of invasive urothelial carcinoma cells. On the contrary, Pyk2, which was strongly activated by IGF-I, was critical for IGF-IR-dependent motility and invasion and regulated IGF-I-dependent activation of the Akt and MAPK pathways. Using immunofluorescence and AQUA analysis we further discovered that Pyk2 was overexpressed in bladder cancer tissues as compared to normal tissue controls. Significantly, in urothelial carcinoma tissues there was increased Pyk2 localization in the nuclei as compared to normal tissue controls. These results provide the first evidence of a specific Pyk2 activity in regulating IGF-IR-dependent motility and invasion of bladder cancer cells suggesting that Pyk2 and the IGF-IR may play a critical role in the invasive phenotype in urothelial neoplasia. In addition, Pyk2 and the IGF-IR may serve as novel biomarkers with diagnostic and prognostic significance in bladder cancer.
胰岛素样生长因子受体 I(IGF-IR)在促进细胞生长和保护癌细胞免受凋亡方面发挥着重要作用,从而促进了转化。我们最近证明,IGF-IR 在浸润性膀胱癌组织中过度表达,并促进尿路上皮癌细胞的迁移和侵袭。这些效应需要 IGF-I 诱导的 Akt 和 MAPK 依赖性的桩蛋白激活。后者与粘着斑激酶(FAK)在动态粘着斑处共定位,对于促进尿路上皮癌细胞的迁移至关重要。FAK 及其同源物富含脯氨酸的酪氨酸激酶 2(Pyk2)调节桩蛋白的激活;然而,它们在调节膀胱癌中 IGF-IR 依赖性信号和迁移中的作用尚未确定。在这项研究中,我们证明 FAK 不是 IGF-IR 依赖性信号和侵袭性尿路上皮癌细胞迁移所必需的。相反,IGF-I 强烈激活的 Pyk2 对于 IGF-IR 依赖性迁移和侵袭以及调节 IGF-IR 依赖性 Akt 和 MAPK 途径的激活至关重要。通过免疫荧光和 AQUA 分析,我们进一步发现 Pyk2 在膀胱癌组织中的表达高于正常组织对照。重要的是,与正常组织对照相比,在尿路上皮癌组织中 Pyk2 定位于细胞核中增加。这些结果首次提供了 Pyk2 活性在调节膀胱癌细胞中 IGF-IR 依赖性迁移和侵袭中的特定作用的证据,表明 Pyk2 和 IGF-IR 可能在尿路上皮肿瘤的侵袭表型中发挥关键作用。此外,Pyk2 和 IGF-IR 可能作为膀胱癌诊断和预后具有重要意义的新型生物标志物。