Liu Y E, Pu W, Jiang Y, Shi D, Dackour R, Shi Y E
Department of Radiation Oncology, Long Island Jewish Medical Center, Albert Einstein College of Medicine, The Feinstein Institute for Medical Research, New Hyde Park, NY 11040, USA.
Oncogene. 2007 Mar 29;26(14):2115-25. doi: 10.1038/sj.onc.1210000. Epub 2006 Oct 2.
Synucleins are emerging as central players in the formation of pathologically insoluble deposits characteristic of neurodegenerative diseases. However, synuclein gamma (SNCG), previously identified as a breast cancer specific gene (BCSG1), is also highly associated with breast cancer progression. Using transgenic mouse model, we demonstrated a role of SNCG in induction of highly proliferative pregnancy-like phenotype of mammary epithelial cells and branching morphology. SNCG participated in the heat shock protein-based multiprotein chaperone complex for steroid receptor signaling. Expression of SNCG in mammary epithelium resulted in a significant stimulation of ERalpha transcriptional activity. SNCG-induced mammary gland proliferation can be effectively blocked by antiestrogen and ovariectomy, indicating that the induced proliferation is mediated by ERalpha signaling and requires estrogen stimulation. These data indicate the chaperone activity of SNCG on stimulation of steroid receptor signaling in mammary gland and, thus induces extensive mammary gland proliferation and contributes to the hormonal impact on mammary tumorigenesis.
突触核蛋白正成为神经退行性疾病特征性病理不可溶性沉积物形成的核心参与者。然而,先前被鉴定为乳腺癌特异性基因(BCSG1)的突触核蛋白γ(SNCG)也与乳腺癌进展高度相关。使用转基因小鼠模型,我们证明了SNCG在诱导乳腺上皮细胞高度增殖的妊娠样表型和分支形态中的作用。SNCG参与了基于热休克蛋白的多蛋白伴侣复合物,用于类固醇受体信号传导。SNCG在乳腺上皮中的表达导致雌激素受体α转录活性的显著刺激。抗雌激素和卵巢切除术可有效阻断SNCG诱导的乳腺增生,表明诱导的增生由雌激素受体α信号传导介导,需要雌激素刺激。这些数据表明SNCG在刺激乳腺类固醇受体信号传导方面的伴侣活性,从而诱导广泛的乳腺增生,并有助于激素对乳腺肿瘤发生的影响。