Bergdorf Kensey, Bauer Joshua A, Westover David, Phifer Courtney, Murphy Barbara, Tyson Darren R, Lee Ethan, Weiss Vivian L
Department of Pharmacology, Vanderbilt University, Nashville, TN 37232, USA.
Department of Biochemistry, Vanderbilt University, Nashville, TN 37232, USA.
Cancers (Basel). 2022 Apr 7;14(8):1855. doi: 10.3390/cancers14081855.
Anaplastic thyroid carcinoma (ATC) is the most aggressive endocrine neoplasm, with a median survival of just four to six months post-diagnosis. Even with surgical and chemotherapeutic interventions, the five-year survival rate is less than 5%. Although combination dabrafenib/trametinib therapy was recently approved for treatment of the ~25% of ATCs harboring mutations, there are no approved, effective treatments for -wildtype disease. Herein, we perform a screen of 1525 drugs and evaluate therapeutic candidates using monolayer cell lines and four corresponding spheroid models of anaplastic thyroid carcinoma. We utilize three-dimensional culture methods, as they have been shown to more accurately recapitulate tumor responses in vivo. These three-dimensional cultures include four distinct ATC spheroid lines representing unique morphology and mutational drivers to provide drug prioritization that will be more readily translatable to the clinic. Using this screen, we identify three exceptionally potent compounds (bortezomib, cabazitaxel, and YM155) that have established safety profiles and could potentially be moved into clinical trial for the treatment of anaplastic thyroid carcinoma, a disease with few treatment options.
间变性甲状腺癌(ATC)是最具侵袭性的内分泌肿瘤,诊断后的中位生存期仅为4至6个月。即使进行手术和化疗干预,五年生存率也低于5%。尽管最近达拉非尼/曲美替尼联合疗法已被批准用于治疗约25%携带特定突变的ATC,但对于野生型疾病尚无获批的有效治疗方法。在此,我们对1525种药物进行筛选,并使用间变性甲状腺癌的单层细胞系和四种相应的球体模型评估治疗候选药物。我们采用三维培养方法,因为已证明它们能更准确地模拟体内肿瘤反应。这些三维培养包括四种不同的ATC球体系,代表独特的形态和突变驱动因素,以提供更易于转化到临床的药物优先级排序。通过该筛选,我们鉴定出三种具有既定安全性且可能推进到治疗间变性甲状腺癌临床试验的强效化合物(硼替佐米、卡巴他赛和YM155),间变性甲状腺癌是一种治疗选择很少的疾病。