Department of Surgery, Biostatistics, and Cancer Biology, and Vanderbilt Center for Quantitative Sciences, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Cancer Res. 2012 Sep 1;72(17):4504-14. doi: 10.1158/0008-5472.CAN-12-1119. Epub 2012 Jun 28.
Esophageal adenocarcinoma (EAC) is an aggressive malignancy with a poor outcome. Although targeting ERBB2 with trastuzumab has been evaluated in clinical trials, the molecular mechanisms of trastuzumab resistance remain uncharacterized in EAC. The dopamine and cyclic AMP-regulated phosphoprotein of MR 32000 (DARPP-32), also known as PPP1R1B, is located together with ERBB2 at the 17q12-q21 amplicon. We evaluated the expression of a transcript variant of DARPP-32 (t-DARPP) and ERBB2 in 141 primary tumors and investigated the role of t-DARPP in trastuzumab resistance using OE19 and OE33 EAC cell models. Overexpression of t-DARPP mRNA was detected in two-thirds of tumors with a correlation between ERBB2 and t-DARPP overexpression levels (r = 0.58, P = 0.003). Cell viability and clonogenic survival assays showed that t-DARPP increased survival by 40% in response to trastuzumab (P < 0.01). The Annexin-V staining and Western blot analysis indicated that t-DARPP effectively abrogated trastuzumab-induced apoptosis, inhibited cleavage of caspase-3, and blocked trastuzumab-induced dephosphorylation of ERBB2 and AKT proteins. The knockdown of endogenous t-DARPP reversed these effects and sensitized cells to trastuzumab (P < 0.01). The cycloheximide-based protein degradation analysis indicated that t-DARPP extended the half-life of ERBB2, explaining the increase in the basal levels of ERBB2, p-ERBB2(Y1248), and p-AKT(S473). Coimmunoprecipitation and Western blot analysis showed that t-DARPP associated with ERBB2 in a protein complex, and interfered with trastuzumab binding to the ERBB2 receptor. Using EAC-xenografted mouse model, t-DARPP enhanced tumor growth and rendered tumors unresponsive to trastuzumab. This study establishes t-DARPP as a mediator of trastuzumab resistance and underscores its potential importance in clinical trials of EAC.
食管腺癌(EAC)是一种侵袭性恶性肿瘤,预后不良。尽管曲妥珠单抗靶向 ERBB2 已在临床试验中进行了评估,但 EAC 中曲妥珠单抗耐药的分子机制仍未得到阐明。多巴胺和环 AMP 调节的磷酸蛋白的 MR 32000(DARPP-32),也称为 PPP1R1B,与 ERBB2 一起位于 17q12-q21 扩增子上。我们评估了 141 个原发性肿瘤中 DARPP-32 的一个转录变体(t-DARPP)和 ERBB2 的表达,并使用 OE19 和 OE33 EAC 细胞模型研究了 t-DARPP 在曲妥珠单抗耐药中的作用。三分之二的肿瘤中检测到 t-DARPP mRNA 的过表达,并且 ERBB2 和 t-DARPP 过表达水平之间存在相关性(r = 0.58,P = 0.003)。细胞活力和集落形成存活测定表明,t-DARPP 使细胞对曲妥珠单抗的存活增加了 40%(P < 0.01)。Annexin-V 染色和 Western blot 分析表明,t-DARPP 有效地阻断了曲妥珠单抗诱导的细胞凋亡,抑制了 caspase-3 的切割,并阻止了曲妥珠单抗诱导的 ERBB2 和 AKT 蛋白的去磷酸化。内源性 t-DARPP 的敲低逆转了这些作用,并使细胞对曲妥珠单抗敏感(P < 0.01)。基于环己酰亚胺的蛋白降解分析表明,t-DARPP 延长了 ERBB2 的半衰期,解释了 ERBB2、p-ERBB2(Y1248)和 p-AKT(S473)基础水平的增加。免疫共沉淀和 Western blot 分析表明,t-DARPP 与 ERBB2 形成蛋白复合物,并干扰了曲妥珠单抗与 ERBB2 受体的结合。使用 EAC 异种移植小鼠模型,t-DARPP 增强了肿瘤生长,并使肿瘤对曲妥珠单抗无反应。这项研究确立了 t-DARPP 作为曲妥珠单抗耐药的介体,并强调了其在 EAC 临床试验中的潜在重要性。