背景(考古学)
生物
癌症研究
表观遗传学
靶向治疗
信号转导
免疫检查点
肺癌
癌症
医学
免疫系统
生物信息学
免疫学
免疫疗法
肿瘤科
基因
遗传学
古生物学
作者
Sally C. M. Lau,Yuanwang Pan,Vamsidhar Velcheti,Kwok‐Kin Wong
出处
期刊:Cancer Cell
[Cell Press]
日期:2022-10-20
卷期号:40 (11): 1279-1293
被引量:86
标识
DOI:10.1016/j.ccell.2022.09.018
摘要
Summary
Squamous cell lung cancers (lung squamous cell carcinomas [LUSCs]) are associated with high mortality and a lack of therapies specific to this disease. Although recurrent molecular aberrations are present in LUSCs, efforts to develop targeted therapies against receptor tyrosine kinases, signaling transduction, and cell cycle checkpoints in LUSCs were met with significant challenges. The present therapeutic landscape focuses on epigenetic therapies to modulate the expression of lineage-dependent survival pathways and undruggable oncogenes. Another important therapeutic approach is to exploit metabolic vulnerabilities unique to LUSCs. These novel therapies may synergize with immune checkpoint inhibitors in the right therapeutic context. For example, the recognition that alterations in KEAP1-NFE2L2 in LUSCs affected antitumor immune responses created unique opportunities for targeted, metabolic, and immune combinations. This article provides a perspective on how lessons learned from the past influence the current therapeutic landscape and opportunities for future drug development for LUSCs.
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