Department of Molecular and Cellular Oncology, MD Anderson Cancer Center, The University of Texas, Houston, TX 77030, USA.
Cancer Cell. 2013 Jun 10;23(6):796-810. doi: 10.1016/j.ccr.2013.04.027.
Epidermal growth factor receptor (EGFR) initiates a signaling cascade that leads to DNA synthesis and cell proliferation, but its role in regulating DNA replication licensing is unclear. Here, we show that activated EGFR phosphorylates the p56 isoform of Lyn, p56(Lyn), at Y32, which then phosphorylates MCM7, a licensing factor critical for DNA replication, at Y600 to increase its association with other minichromosome maintenance complex proteins, thereby promoting DNA synthesis complex assembly and cell proliferation. Both p56(Lyn) Y32 and MCM7 Y600 phosphorylation are enhanced in proliferating cells and correlated with poor survival of breast cancer patients. These results establish a signaling cascade in which EGFR enhances MCM7 phosphorylation and DNA replication through Lyn phosphorylation in human cancer cells.
表皮生长因子受体 (EGFR) 启动信号级联反应,导致 DNA 合成和细胞增殖,但它在调节 DNA 复制许可中的作用尚不清楚。在这里,我们表明激活的 EGFR 在 Y32 位点磷酸化 Lyn 的 p56 同工型,p56(Lyn),然后 p56(Lyn) 在 Y600 位点磷酸化 MCM7,MCM7 是 DNA 复制的关键许可因子,以增加其与其他微染色体维持复合物蛋白的结合,从而促进 DNA 合成复合物组装和细胞增殖。增殖细胞中 p56(Lyn) Y32 和 MCM7 Y600 磷酸化均增强,并且与乳腺癌患者的不良生存相关。这些结果建立了一个信号级联,其中 EGFR 通过 Lyn 在人类癌细胞中的磷酸化增强 MCM7 磷酸化和 DNA 复制。