靶向治疗
医学
后天抵抗
癌症
癌症研究
疾病
癌基因
内科学
细胞周期
作者
Sandra Ortiz‐Cuaran,Camille Léonce
标识
DOI:10.1158/1078-0432.ccr-24-3734
摘要
Summary The success of targeted therapies in oncogene-driven cancer is limited by adaptive or acquired treatment resistance, leading to disease progression. A recent study reports that YAP-dependent human epidermal growth factor receptor 3 (HER3) activation constitutes a therapeutic vulnerability of adaptive resistance to RET-targeted therapies in RET-altered cancers, highlighting a promising strategy to improve RET inhibitor tumor responses. See related article by Katayama et al., p. 1127
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