Small cell lung cancer profiling: an updated synthesis of subtypes, vulnerabilities, and plasticity

被引:11
作者
Redin, Esther [1 ]
Quintanal-Villalonga, Alvaro [1 ]
Rudin, Charles M. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Thorac Oncol Serv, Dept Med, New York, NY 10065 USA
[2] Weill Cornell Med, Pharmacol Program, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
MOLECULAR SUBTYPES; MOUSE MODEL; OPEN-LABEL; NEUROENDOCRINE; SCLC; ORIGIN; ASCL1; HETEROGENEITY; RESISTANCE; TUMORS;
D O I
10.1016/j.trecan.2024.07.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Small cell lung cancer (SCLC) is a devastating disease with high proliferative and metastatic capacity. SCLC has been classified into molecular subtypes based on differential expression of lineage-defining transcription factors. Recent studies have proposed new subtypes that are based on both tumor-intrinsic and -extrinsic factors. SCLC demonstrates substantial intratumoral subtype heterogeneity characterized by highly plastic transcriptional states, indicating that the initially dominant subtype can shift during disease progression and in association with resistance to therapy. Strategies to promote or constrain plasticity and cell fate transitions have nominated novel targets that could prompt the development of more durably effective therapies for patients with SCLC. In this review, we describe the latest advances in SCLC subtype classification and their biological and clinical implications.
引用
收藏
页码:935 / 946
页数:12
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