蛋白质酪氨酸磷酸酶
变构调节
原癌基因酪氨酸蛋白激酶Src
受体酪氨酸激酶
信号转导
细胞生物学
MAPK/ERK通路
激酶
酪氨酸激酶
磷酸酶
磷酸化
蛋白酪氨酸激酶
化学
癌症研究
生物
受体
生物化学
作者
Alessia Petrocchi,A Ciammaichella
标识
DOI:10.1080/13543776.2024.2365410
摘要
Multiple potent allosteric SHP2 inhibitors have been discovered, disclosed, and tested in a variety of preclinical cancer models with strong evidence of efficacy. Fifteen compounds are currently in clinical development, but none of them have been approved for marketing. Until now, long-term benefit of SHP2 inhibitors as monotherapy agents have not been demonstrated due to acquired mechanisms of resistance and/or lack of efficacy. However, combination therapies with a variety of agents, such as MEK, BRAF, EGFR, RAS-G12C and PDL-1 inhibitors, have high potential and are currently an extensive area of investigation.
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