Xia Wenle, Liu Lei-Hua, Ho Peter, Spector Neil L
Department of Discovery Medicine, GlaxoSmithKline, Five Moore Drive, Research Triangle Park, NC 27709-3398, USA.
Oncogene. 2004 Jan 22;23(3):646-53. doi: 10.1038/sj.onc.1207166.
The expression of the NH2 terminally truncated ErbB2 receptor (p95ErbB2) in breast cancer correlates with metastatic disease progression compared with the expression of full-length p185ErbB2. We now show that heregulin (HRG), but not EGF, stimulates p95ErbB2 phosphorylation in BT474 breast cancer cells. Furthermore, phospho-p95ErbB2 forms heterodimers with ErbB3, but not EGFR, while p185ErbB2 heterodimerizes with both EGFR and ErbB3. The predilection of p95ErbB2 to heterodimerize with ErbB3 provides an explanation for its regulation by HRG, an ErbB3 ligand. GW572016, a reversible small molecule inhibitor of EGFR and ErbB2 tyrosine kinases, inhibits baseline p95ErbB2 phosphorylation in BT474 cells and tumor xenografts. Inhibition of p95ErbB2, p185ErbB2, and EGFR phosphorylation by GW572016 resulted in the inhibition of downstream phospho-Erk1/2, phospho-AKT, and cyclin D steady-state protein levels. Increased phosphorylation of p95ErbB2 and AKT in response to HRG was abrogated to varying degrees by GW572016. In contrast, trastuzumab did not inhibit p95ErbB2 phosphorylation or the expression of downstream phospho-Erk1/2, phospho-AKT, or cyclin D. It is tempting to speculate that trastuzumab resistance may be mediated in part by the selection of p95ErbB2-expressing breast cancer cells capable of exerting potent growth and prosurvival signals through p95ErbB2-ErbB3 heterodimers. Thus, p95ErbB2 represents a target for therapeutic intervention, and one that is sensitive to GW572016 therapy.
与全长p185ErbB2的表达相比,乳腺癌中氨基末端截短的ErbB2受体(p95ErbB2)的表达与转移性疾病进展相关。我们现在表明,在这里调节蛋白(HRG)而非表皮生长因子(EGF)可刺激BT474乳腺癌细胞中的p95ErbB2磷酸化。此外,磷酸化的p95ErbB2与ErbB3而非表皮生长因子受体(EGFR)形成异二聚体,而p185ErbB2则与EGFR和ErbB3均形成异二聚体。p95ErbB2倾向于与ErbB3形成异二聚体,这为其受ErbB3配体HRG的调节提供了解释。GW572016是一种EGFR和ErbB2酪氨酸激酶的可逆小分子抑制剂,可抑制BT474细胞和肿瘤异种移植物中p95ErbB2的基础磷酸化。GW572016对p95ErbB2、p185ErbB2和EGFR磷酸化的抑制导致下游磷酸化细胞外信号调节激酶1/2(phospho-Erk1/2)、磷酸化蛋白激酶B(phospho-AKT)和细胞周期蛋白D稳态蛋白水平的抑制。GW572016不同程度地消除了HRG诱导的p95ErbB2和AKT磷酸化增加。相比之下,曲妥珠单抗不抑制p95ErbB2磷酸化或下游phospho-Erk1/2、phospho-AKT或细胞周期蛋白D的表达。很容易推测,曲妥珠单抗耐药性可能部分是由选择能够通过p95ErbB2-ErbB3异二聚体发出强大生长和促生存信号的p95ErbB2表达乳腺癌细胞介导的。因此,p95ErbB2是治疗干预的一个靶点,并且是对GW572016治疗敏感的靶点。