Division of Oncology, Department of Medicine.
Lineberger Comprehensive Cancer Center.
J Clin Invest. 2021 Nov 15;131(22). doi: 10.1172/JCI154095.
Despite recent therapeutic gains in the treatment of advanced bladder cancer, the overall survival in patients with metastatic disease remains poor and further therapeutic discovery is needed. Advanced bladder cancer is a molecularly heterogeneous disease, and the identification of driver genetic alterations has led to effective targeted therapeutic agents, such as fibroblast growth factor receptor (FGFR) inhibitors. In this issue of the JCI, Bekele et al. identify a subtype of muscle-invasive bladder cancer (MIBC) that harbors RAF1 amplification. The authors showed that RAF1 inhibition, with pan-RAF inhibitors, and the combination of RAF1 inhibition with MEK inhibition were efficacious in preclinical models harboring RAF1 amplifications as well as in tumors with HRAS and NRAS mutations. This study highlights RAF1 amplification as a driver event in bladder cancer and establishes the central role of the MAPK pathway in bladder tumorigenesis.
尽管在治疗晚期膀胱癌方面最近取得了治疗进展,但转移性疾病患者的总体生存率仍然较差,需要进一步的治疗发现。晚期膀胱癌是一种分子异质性疾病,对驱动基因突变的鉴定已导致了有效的靶向治疗药物的出现,如成纤维细胞生长因子受体(FGFR)抑制剂。在本期 JCI 中,Bekele 等人鉴定出一种肌层浸润性膀胱癌(MIBC)亚型,其存在 RAF1 扩增。作者表明,RAF1 抑制,包括 pan-RAF 抑制剂,以及 RAF1 抑制与 MEK 抑制的联合应用,在携带 RAF1 扩增的临床前模型以及具有 HRAS 和 NRAS 突变的肿瘤中均有效。这项研究强调了 RAF1 扩增作为膀胱癌的驱动事件,并确立了 MAPK 通路在膀胱癌发生中的核心作用。