Bangi Erdem, Smibert Peter, Uzilov Andrew V, Teague Alexander G, Gopinath Sindhura, Antipin Yevgeniy, Chen Rong, Hecht Chana, Gruszczynski Nelson, Yon Wesley J, Malyshev Denis, Laspina Denise, Selkridge Isaiah, Wang Huan, Gomez Jorge, Mascarenhas John, Moe Aye S, Lau Chun Yee, Taik Patricia, Pandya Chetanya, Sung Max, Kim Sara, Yum Kendra, Sebra Robert, Donovan Michael, Misiukiewicz Krzysztof, Ang Celina, Schadt Eric E, Posner Marshall R, Cagan Ross L
Department of Cell, Development, and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Department of Genetics and Genomic Sciences and Icahn Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
iScience. 2021 Feb 20;24(3):102212. doi: 10.1016/j.isci.2021.102212. eCollection 2021 Mar 19.
Adenoid cystic carcinoma (ACC) is a rare cancer type that originates in the salivary glands. Tumors commonly invade along nerve tracks in the head and neck, making surgery challenging. Follow-up treatments for recurrence or metastasis including chemotherapy and targeted therapies have shown limited efficacy, emphasizing the need for new therapies. Here, we report a Drosophila-based therapeutic approach for a patient with advanced ACC disease. A patient-specific Drosophila transgenic line was developed to model the five major variants associated with the patient's disease. Robotics-based screening identified a three-drug cocktail-vorinostat, pindolol, tofacitinib-that rescued transgene-mediated lethality in the Drosophila patient-specific line. Patient treatment led to a sustained stabilization and a partial metabolic response of 12 months. Subsequent resistance was associated with new genomic amplifications and deletions. Given the lack of options for patients with ACC, our data suggest that this approach may prove useful for identifying novel therapeutic candidates.
腺样囊性癌(ACC)是一种起源于唾液腺的罕见癌症类型。肿瘤通常沿头颈部神经通路浸润,这使得手术具有挑战性。针对复发或转移的后续治疗,包括化疗和靶向治疗,疗效有限,这凸显了新疗法的必要性。在此,我们报告了一种基于果蝇的针对晚期ACC疾病患者的治疗方法。开发了一种患者特异性果蝇转基因系,以模拟与该患者疾病相关的五种主要变体。基于机器人技术的筛选确定了一种三联药物组合——伏立诺他、吲哚洛尔、托法替布——可挽救果蝇患者特异性系中转基因介导的致死性。患者接受治疗后病情持续稳定,并出现了为期12个月的部分代谢反应。随后的耐药性与新的基因组扩增和缺失有关。鉴于ACC患者缺乏治疗选择,我们的数据表明,这种方法可能有助于识别新的治疗候选药物。