串扰
信号转导
MAPK/ERK通路
癌症研究
蛋白激酶B
抗药性
细胞信号
医学
生物信息学
生物
细胞生物学
遗传学
光学
物理
作者
Xuejian Wang,Wenyan Jiang,Yanmei Du,Zhu Dongqi,Jian Zhang,Chunyan Fang,Yan Fang,Zhe-Sheng Chen
标识
DOI:10.1016/j.drup.2022.100884
摘要
Dysregulation or aberrant signaling transduction contributes to tumorigenesis. Targeting these abnormal signaling pathways becomes an effective anticancer strategy. However, feedback activation or crosstalk between signaling pathways drives adaptive drug resistance which causes failure of cancer therapy. In this review article, we summarized treatments that cause feedback activation of AKT, ERK, STAT3, EGFR, FGFR, and HER2/3 signaling pathways and the combination therapy to enhance anti-tumor effect or to overcome drug resistance, to explore the underlying mechanisms that define the protein molecules participated or regulated the feedback activation. In addition, we reviewed clinical trials that employ combination treatments to suppress feedback activation and improve therapeutic efficacy of cancer treatments.
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