Department of Thoracic Surgery, Comprehensive Cancer Center, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Department of Thoracic Surgery, Semmelweis University and National Institute of Oncology, Budapest, Hungary.
Mol Cancer. 2024 Feb 24;23(1):41. doi: 10.1186/s12943-024-01953-9.
Current treatment guidelines refer to small cell lung cancer (SCLC), one of the deadliest human malignancies, as a homogeneous disease. Accordingly, SCLC therapy comprises chemoradiation with or without immunotherapy. Meanwhile, recent studies have made significant advances in subclassifying SCLC based on the elevated expression of the transcription factors ASCL1, NEUROD1, and POU2F3, as well as on certain inflammatory characteristics. The role of the transcription regulator YAP1 in defining a unique SCLC subset remains to be established. Although preclinical analyses have described numerous subtype-specific characteristics and vulnerabilities, the so far non-existing clinical subtype distinction may be a contributor to negative clinical trial outcomes. This comprehensive review aims to provide a framework for the development of novel personalized therapeutic approaches by compiling the most recent discoveries achieved by preclinical SCLC research. We highlight the challenges faced due to limited access to patient material as well as the advances accomplished by implementing state-of-the-art models and methodologies.
目前的治疗指南将小细胞肺癌(SCLC)视为一种致命的人类恶性肿瘤,将其视为一种同质疾病。因此,SCLC 的治疗包括放化疗加或不加免疫疗法。与此同时,最近的研究在基于转录因子 ASCL1、NEUROD1 和 POU2F3 的高表达以及某些炎症特征对 SCLC 进行亚分类方面取得了重大进展。转录调节剂 YAP1 在定义独特的 SCLC 亚群中的作用尚待确定。尽管临床前分析已经描述了许多亚型特异性特征和脆弱性,但迄今为止尚未存在的临床亚型区分可能是临床试验结果不佳的原因之一。本综述旨在通过汇集临床前 SCLC 研究的最新发现,为开发新型个性化治疗方法提供框架。我们强调了由于获取患者材料有限而面临的挑战,以及通过实施最先进的模型和方法所取得的进展。