Department of Head and Neck Cancer, Instituto de Investigación Sanitaria del Principado de Asturias, 33011 Oviedo, Spain.
Department of Pathology, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.
Int J Mol Sci. 2023 Oct 12;24(20):15110. doi: 10.3390/ijms242015110.
Despite advances in surgery and radiotherapy, the overall prognosis of sinonasal intestinal-type adenocarcinoma (ITAC) is poor, and new treatment options are needed. Recent studies have indicated alterations in cellular signaling pathways that may serve as targets for modern inhibitors. Our aim was to evaluate the frequency of mTOR and ERK pathway upregulation in a retrospective series of 139 ITAC and to test the efficacy and mechanism of action of candidate targeted inhibitors in cell line ITAC-3. An immunohistochemical analysis on p-AKT, p-mTOR, p-S6, p-4E-BP1, and p-ERK indicated, respectively, a 68% and 57% mTOR and ERK pathway activation. In vitro studies using low doses of mTOR inhibitor everolimus and ERK inhibitor selumetinib showed significant growth inhibition as monotherapy and especially as combined therapy. This effect was accompanied by the downregulation of mTOR and ERK protein expression. Our data open a new and promising possibility for personalized treatment of ITAC patients.
尽管手术和放疗取得了进展,但鼻腔鼻窦肠型腺癌(ITAC)的总体预后仍然较差,需要新的治疗选择。最近的研究表明,细胞信号通路的改变可能成为现代抑制剂的作用靶点。我们的目的是在 139 例 ITAC 的回顾性系列中评估 mTOR 和 ERK 通路上调的频率,并在细胞系 ITAC-3 中测试候选靶向抑制剂的疗效和作用机制。免疫组化分析显示 p-AKT、p-mTOR、p-S6、p-4E-BP1 和 p-ERK 分别有 68%和 57%的 mTOR 和 ERK 通路激活。使用低剂量 mTOR 抑制剂依维莫司和 ERK 抑制剂 selumetinib 的体外研究表明,单药治疗和联合治疗均有明显的生长抑制作用。这种作用伴随着 mTOR 和 ERK 蛋白表达的下调。我们的数据为 ITAC 患者的个体化治疗开辟了一个新的、有前途的可能性。