State Key Laboratory of Biotherapy, Section of Signal Transduction and Molecular Targeted Therapy, West China Hospital, Sichuan University, Chengdu 610041, China.
J Biol Chem. 2010 Oct 1;285(40):30480-8. doi: 10.1074/jbc.M110.131698. Epub 2010 Jul 29.
Insulin-like growth factor (IGF) system plays important roles in carcinogenesis and maintenance of the malignant phenotype. Signaling through the IGF-I receptor (IGF-IR) has been shown to stimulate the growth and motility of a wide range of cancer cells. γ-synuclein (SNCG) is primarily expressed in peripheral neurons but also overexpressed in various cancer cells. Overexpression of SNCG correlates with tumor progression. In the present study we demonstrated a reciprocal regulation of IGF-I signaling and SNCG expression. IGF-I induced SNCG expression in various cancer cells. IGF-IR knockdown or IGF-IR inhibitor repressed SNCG expression. Both phosphatidylinositol 3-kinase and mitogen-activated protein kinase were involved in IGF-I induction of SNCG expression. Interestingly, SNCG knockdown led to proteasomal degradation of IGF-IR, thereby decreasing the steady-state levels of IGF-IR. Silencing of SNCG resulted in a decrease in ligand-induced phosphorylation of IGF-IR and its downstream signaling components, including insulin receptor substrate (IRS), Akt, and ERK1/2. Strikingly, SNCG physically interacted with IGF-IR and IRS-2. Silencing of IRS-2 impaired the interaction between SNCG and IGF-IR. Finally, SNCG knockdown suppressed IGF-I-induced cell proliferation and migration. These data reveal that SNCG and IGF-IR are mutually regulated by each other. SNCG blockade may suppress IGF-I-induced cell proliferation and migration. Conversely, IGF-IR inhibitors may be of utility in suppressing the aberrant expression of SNCG in cancer cells and thereby block its pro-tumor effects.
胰岛素样生长因子(IGF)系统在致癌作用和恶性表型的维持中发挥重要作用。IGF-I 受体(IGF-IR)的信号转导已被证明能刺激广泛的癌细胞的生长和迁移。γ-突触核蛋白(SNCG)主要在外周神经元中表达,但也在各种癌细胞中过度表达。SNCG 的过表达与肿瘤进展相关。在本研究中,我们证明了 IGF-I 信号和 SNCG 表达之间存在相互调节。IGF-I 诱导各种癌细胞中的 SNCG 表达。IGF-IR 敲低或 IGF-IR 抑制剂抑制 SNCG 表达。PI3K 和 MAPK 均参与 IGF-I 诱导的 SNCG 表达。有趣的是,SNCG 敲低导致 IGF-IR 的蛋白酶体降解,从而降低 IGF-IR 的稳态水平。SNCG 的沉默导致配体诱导的 IGF-IR 及其下游信号成分(包括胰岛素受体底物(IRS)、Akt 和 ERK1/2)的磷酸化减少。引人注目的是,SNCG 与 IGF-IR 和 IRS-2 相互作用。沉默 IRS-2 会损害 SNCG 与 IGF-IR 之间的相互作用。最后,SNCG 敲低抑制了 IGF-I 诱导的细胞增殖和迁移。这些数据表明 SNCG 和 IGF-IR 相互调节。SNCG 阻断可能抑制 IGF-I 诱导的细胞增殖和迁移。相反,IGF-IR 抑制剂可能有助于抑制癌细胞中 SNCG 的异常表达,并阻断其促肿瘤作用。