Department of Biochemistry and Molecular Biology, College of Medicine, University of Nebraska Medical Center, 985870 Nebraska Medical Center, Omaha, NE, 68198-5870, USA.
Cancer Metastasis Rev. 2010 Mar;29(1):207-22. doi: 10.1007/s10555-010-9213-8.
p66Shc, a 66 kDa proto-oncogene Src homologous-collagen homologue (Shc) adaptor protein, is classically known in mediating receptor tyrosine kinase signaling and recently identified as a sensor to oxidative stress-induced apoptosis and as a longevity protein in mammals. The expression of p66Shc is decreased in mice and increased in human fibroblasts upon aging and in aging-related diseases, including prostate cancer. p66Shc protein level correlates with the proliferation of several carcinoma cells and can be regulated by steroid hormones. Recent advances point that p66Shc protein plays a role in mediating cross-talk between steroid hormones and redox signals by serving as a common convergence point in signaling pathways on cell proliferation and apoptosis. This article first reviews the unique function of p66Shc protein in regulating oxidative stress-induced apoptosis. Subsequently, we discuss its novel role in androgen-regulated prostate cancer cell proliferation and metastasis and the mechanism by which it mediates androgen action via the redox signaling pathway. The data together indicate that p66Shc might be a useful biomarker for the prognosis of prostate cancer and serve as an effective target for its cancer treatment.
p66Shc 是一种 66kDa 的原癌基因 Src 同源胶原同源物(Shc)衔接蛋白,经典地介导受体酪氨酸激酶信号转导,最近被鉴定为氧化应激诱导细胞凋亡的传感器和哺乳动物的长寿蛋白。p66Shc 的表达在衰老和衰老相关疾病(包括前列腺癌)中在小鼠中降低,在人类成纤维细胞中增加。p66Shc 蛋白水平与几种癌细胞的增殖相关,并可被类固醇激素调节。最近的进展表明,p66Shc 蛋白在介导甾体激素和氧化还原信号之间的串扰中发挥作用,作为细胞增殖和凋亡信号通路的共同汇聚点。本文首先综述了 p66Shc 蛋白在调节氧化应激诱导细胞凋亡中的独特功能。随后,我们讨论了它在雄激素调节的前列腺癌细胞增殖和转移中的新作用,以及它通过氧化还原信号通路介导雄激素作用的机制。这些数据表明,p66Shc 可能是前列腺癌预后的有用生物标志物,并可作为其癌症治疗的有效靶点。