Zarzosa Patricia, Garcia-Gilabert Lia, Hladun Raquel, Guillén Gabriela, Gallo-Oller Gabriel, Pons Guillem, Sansa-Girona Julia, Segura Miguel F, Sánchez de Toledo Josep, Moreno Lucas, Gallego Soledad, Roma Josep
Childhood Cancer and Blood Disorders, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.
Pediatric Oncology and Hematology Department, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.
Cancers (Basel). 2023 Jan 24;15(3):727. doi: 10.3390/cancers15030727.
Aberrant activation of the Hedgehog (Hh) signalling pathway is known to play an oncogenic role in a wide range of cancers; in the particular case of rhabdomyosarcoma, this pathway has been demonstrated to be an important player for both oncogenesis and cancer progression. In this review, after a brief description of the pathway and the characteristics of its molecular components, we describe, in detail, the main activation mechanisms that have been found in cancer, including ligand-dependent, ligand-independent and non-canonical activation. In this context, the most studied inhibitors, i.e., SMO inhibitors, have shown encouraging results for the treatment of basal cell carcinoma and medulloblastoma, both tumour types often associated with mutations that lead to the activation of the pathway. Conversely, SMO inhibitors have not fulfilled expectations in tumours-among them sarcomas-mostly associated with ligand-dependent Hh pathway activation. Despite the controversy existing regarding the results obtained with SMO inhibitors in these types of tumours, several compounds have been (or are currently being) evaluated in sarcoma patients. Finally, we discuss some of the reasons that could explain why, in some cases, encouraging preclinical data turned into disappointing results in the clinical setting.
已知刺猬索尼克(Hh)信号通路的异常激活在多种癌症中发挥致癌作用;在横纹肌肉瘤这种特定情况下,该通路已被证明是肿瘤发生和癌症进展的重要参与者。在这篇综述中,在简要描述该通路及其分子成分的特征之后,我们详细描述了在癌症中发现的主要激活机制,包括配体依赖性、配体非依赖性和非经典激活。在此背景下,研究最多的抑制剂,即 smoothened(SMO)抑制剂,已在基底细胞癌和髓母细胞瘤的治疗中显示出令人鼓舞的结果,这两种肿瘤类型通常与导致该通路激活的突变相关。相反,SMO 抑制剂在主要与配体依赖性 Hh 通路激活相关的肿瘤(包括肉瘤)中并未达到预期效果。尽管在这些类型的肿瘤中使用 SMO 抑制剂所获得的结果存在争议,但几种化合物已在(或正在)肉瘤患者中进行评估。最后,我们讨论了一些原因,这些原因可以解释为什么在某些情况下,令人鼓舞的临床前数据在临床环境中却变成了令人失望的结果。