Program in Oral and Craniofacial Biomedicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Department of Pharmacology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Mol Cancer Ther. 2022 May 4;21(5):762-774. doi: 10.1158/1535-7163.MCT-21-0142.
Human papilloma virus (HPV)-negative head and neck squamous cell carcinoma (HNSCC) is a common cancer worldwide with an unmet need for more effective, less toxic treatments. Currently, both the disease and the treatment of HNSCC cause significant mortality and morbidity. Targeted therapies hold new promise for patients with HPV-negative status whose tumors harbor oncogenic HRAS mutations. Recent promising clinical results have renewed interest in the development of farnesyltransferase inhibitors (FTIs) as a therapeutic strategy for HRAS-mutant cancers. With the advent of clinical evaluation of the FTI tipifarnib for the treatment of HRAS-mutant HNSCC, we investigated the activity of tipifarnib and inhibitors of HRAS effector signaling in HRAS-mutant HNSCC cell lines. First, we validated that HRAS is a cancer driver in HRAS-mutant HNSCC lines. Second, we showed that treatment with the FTI tipifarnib largely phenocopied HRAS silencing, supporting HRAS as a key target of FTI antitumor activity. Third, we performed reverse-phase protein array analyses to profile FTI treatment-induced changes in global signaling, and conducted CRISPR/Cas9 genetic loss-of-function screens to identify previously unreported genes and pathways that modulate sensitivity to tipifarnib. Fourth, we determined that concurrent inhibition of HRAS effector signaling (ERK, PI3K, mTORC1) increased sensitivity to tipifarnib treatment, in part by overcoming tipifarnib-induced compensatory signaling. We also determined that ERK inhibition could block tipifarnib-induced epithelial-to-mesenchymal transition, providing a potential basis for the effectiveness of this combination. Our results support future investigations of these and other combination treatments for HRAS mutant HNSCC.
人乳头瘤病毒(HPV)阴性的头颈部鳞状细胞癌(HNSCC)是一种常见的癌症,全球范围内都存在着对更有效、毒性更小的治疗方法的需求。目前,HNSCC 的疾病和治疗都会导致显著的死亡率和发病率。针对 HPV 阴性患者的靶向治疗有望取得新进展,这些患者的肿瘤携带有致癌性 HRAS 突变。最近令人鼓舞的临床结果重新激发了人们对法呢基转移酶抑制剂(FTIs)作为治疗 HRAS 突变癌症的一种治疗策略的兴趣。随着 FTI 替匹法尼布用于治疗 HRAS 突变 HNSCC 的临床评估的出现,我们研究了替匹法尼布和 HRAS 效应信号抑制剂在 HRAS 突变 HNSCC 细胞系中的活性。首先,我们验证了 HRAS 是 HRAS 突变 HNSCC 系中的致癌驱动基因。其次,我们表明,FTI 替匹法尼布的治疗在很大程度上模拟了 HRAS 沉默,支持 HRAS 作为 FTI 抗肿瘤活性的关键靶点。第三,我们进行了反相蛋白阵列分析,以描绘 FTI 治疗诱导的全局信号变化,并进行了 CRISPR/Cas9 基因敲除功能筛选,以鉴定以前未报道的基因和通路,这些基因和通路调节对替匹法尼布的敏感性。第四,我们确定同时抑制 HRAS 效应信号(ERK、PI3K、mTORC1)增加了对替匹法尼布治疗的敏感性,部分原因是克服了替匹法尼布诱导的代偿性信号。我们还确定 ERK 抑制可以阻断替匹法尼布诱导的上皮间质转化,为这种联合治疗的有效性提供了潜在的基础。我们的研究结果支持对这些和其他针对 HRAS 突变 HNSCC 的联合治疗进行进一步研究。