Department of Biochemistry, School of Medicine, West Virginia University, Morgantown, WV 26506, USA.
Oncogene. 2013 Aug 29;32(35):4169-80. doi: 10.1038/onc.2012.418. Epub 2012 Oct 1.
One of the causes of breast cancer is overexpression of the human epidermal growth factor receptor 2 (HER2). Enhanced receptor autophosphorylation and resistance to activation-induced downregulation have been suggested as mechanisms for HER2-induced sustained signaling and cell transformation. However, the molecular mechanisms underlying these possibilities remain incompletely understood. In the current report, we present evidence that show that HER2 overexpression does not lead to receptor hyper-autophosphorylation, but alters patterns in a manner that favors receptor stability and sustained signaling. Specifically, HER2 overexpression blocks epidermal growth factor receptor (EGFR) tyrosine phosphorylation on Y1045 and Y1068, the known docking sites of c-Cbl and Grb2, respectively, whereas promoting phosphorylation on Y1173, the known docking site of the Gab adaptor proteins and phospholipase C gamma. Under these conditions, HER2 itself is phosphorylated on Y1221/1222, with no known role, and on Y1248 that corresponds to Y1173 of EGFR. Interestingly, suppressed EGFR autophosphorylation on the Grb2 and c-Cbl-binding sites correlated with receptor stability and sustained signaling, suggesting that HER2 accomplishes these tasks by altering autophosphorylation patterns. In conformity with these findings, mutation of the Grb2-binding site on EGFR (Y1068F-EGFR) conferred resistance to ligand-induced degradation, which in turn induced sustained signaling, and increased cell proliferation and transformation. These findings suggest that the Grb2-binding site on EGFR is redundant for signaling, but critical for receptor regulation. On the other hand, mutation of the putative Grb2-binding site in HER2 (Y1139) did not affect stability, signaling or transformation, suggesting that Y1139 in HER2 may not serve as a Grb2-binding site. In agreement with the role of EGFR in HER2 signaling, inhibition of EGFR expression reduced HER2-induced anchorage-independent growth and tumorigenesis. These results imply that complementing HER2-targeted therapies with anti-EGFR drugs may be beneficial in HER2-positive breast cancer.
乳腺癌的一个成因是人类表皮生长因子受体 2(HER2)的过度表达。增强的受体自动磷酸化和对激活诱导的下调的抗性被认为是 HER2 诱导持续信号转导和细胞转化的机制。然而,这些可能性的分子机制仍不完全了解。在本报告中,我们提供的证据表明,HER2 的过度表达不会导致受体过度自动磷酸化,而是以有利于受体稳定性和持续信号转导的方式改变模式。具体而言,HER2 的过度表达阻止了表皮生长因子受体(EGFR)在 Y1045 和 Y1068 上的酪氨酸磷酸化,这分别是 c-Cbl 和 Grb2 的已知 docking 位点,而促进了 Y1173 上的磷酸化,这是 Gab 衔接蛋白和磷脂酶 Cγ的已知 docking 位点。在这些条件下,HER2 本身在 Y1221/1222 上磷酸化,该位点没有已知的作用,并且在 Y1248 上磷酸化,该位点对应于 EGFR 的 Y1173。有趣的是,EGFR 上 Grb2 和 c-Cbl 结合位点的抑制性自动磷酸化与受体稳定性和持续信号转导相关,表明 HER2 通过改变自动磷酸化模式来完成这些任务。与这些发现一致,EGFR 上 Grb2 结合位点(Y1068F-EGFR)的突变赋予了对配体诱导降解的抗性,这反过来又诱导了持续的信号转导,并增加了细胞增殖和转化。这些发现表明,EGFR 上的 Grb2 结合位点对于信号转导是冗余的,但对于受体调节却是关键的。另一方面,HER2 中假定的 Grb2 结合位点(Y1139)的突变不影响稳定性、信号转导或转化,表明 HER2 中的 Y1139 可能不是 Grb2 结合位点。与 EGFR 在 HER2 信号转导中的作用一致,抑制 EGFR 表达降低了 HER2 诱导的非锚定依赖性生长和肿瘤发生。这些结果表明,用抗 EGFR 药物补充 HER2 靶向治疗可能有益于 HER2 阳性乳腺癌。