Targeting ERK, an Achilles' Heel of the MAPK pathway, in cancer therapy

被引:498
作者
Liu, Feifei [1 ]
Yang, Xiaotong [1 ]
Geng, Meiyu [1 ]
Huang, Min [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, Div Antitumor Pharmacol, State Key Lab Drug Res, Shanghai 201203, Peoples R China
关键词
Mitogen-activated protein kinases; Extracellular signal-regulated kinase; ERK inhibitor; ERK kinase; Cancer therapy; Drug resistance; INHIBITOR-RESISTANT MELANOMA; RENAL-CELL CARCINOMA; ACQUIRED-RESISTANCE; MEK INHIBITORS; K-RAS; FEEDBACK PHOSPHORYLATION; SIGNALING PATHWAY; PLASMA-MEMBRANE; GENE-EXPRESSION; SMALL MOLECULES;
D O I
10.1016/j.apsb.2018.01.008
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The mitogen-activated protein kinases (MAPK) pathway, often known as the RAS-RAF-MEK-ERK signal cascade, functions to transmit upstream signals to its downstream effectors to regulate physiological process such as cell proliferation, differentiation, survival and death. As the most frequently mutated signaling pathway in human cancer, targeting the MAPK pathway has long been considered a promising strategy for cancer therapy. Substantial efforts in the past decades have led to the clinical success of BRAF and MEK inhibitors. However, the clinical benefits of these inhibitors are compromised by the frequently occurring acquired resistance due to cancer heterogeneity and genomic instability. This review briefly introduces the key protein kinases involved in this pathway as well as their activation mechanisms. We also generalize the correlations between mutations of MAPK members and human cancers, followed by a summarization of progress made on the development of small molecule MAPK kinases inhibitors. In particular, this review highlights the potential advantages of ERK inhibitors in overcoming resistance to upstream targets and proposes that targeting ERK kinase may hold a promising prospect for cancer therapy. (C) 2018 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:552 / 562
页数:11
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