JNK signalling in cancer: in need of new, smarter therapeutic targets

被引:306
作者
Bubici, Concetta [1 ,2 ]
Papa, Salvatore [3 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Med, Sect Inflammat & Signal Transduct, London W12 0NN, England
[2] Brunel Univ, Sch Hlth Sci & Social Care, Biosci Div, London, England
[3] Fdn Liver Res, Inst Hepatol, Cell Signaling & Canc Lab, London, England
关键词
JNK1; JNK2; PARP14; survival; apoptosis; multiple myeloma; hepatocellular carcinoma; cancer targets; N-TERMINAL KINASE; JUN NH2-TERMINAL KINASE; C-JUN; KAPPA-B; MULTIPLE-MYELOMA; PEPTIDE INHIBITOR; CHEMICAL HEPATOCARCINOGENESIS; BIOLOGIC SEQUELAE; TUMOR-GROWTH; IKK-BETA;
D O I
10.1111/bph.12432
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The JNKs are master protein kinases that regulate many physiological processes, including inflammatory responses, morphogenesis, cell proliferation, differentiation, survival and death. It is increasingly apparent that persistent activation of JNKs is involved in cancer development and progression. Therefore, JNKs represent attractive targets for therapeutic intervention with small molecule kinase inhibitors. However, evidence supportive of a tumour suppressor role for the JNK proteins has also been documented. Recent studies showed that the two major JNK proteins, JNK1 and JNK2, have distinct or even opposing functions in different types of cancer. As such, close consideration of which JNK proteins are beneficial targets and, more importantly, what effect small molecule inhibitors of JNKs have on physiological processes, are essential. A number of ATP-competitive and ATP-non-competitive JNK inhibitors have been developed, but have several limitations such as a lack of specificity and cellular toxicity. In this review, we summarize the accumulating evidence supporting a role for the JNK proteins in the pathogenesis of different solid and haematological malignancies, and discuss many challenges and scientific opportunities in the targeting of JNKs in cancer.
引用
收藏
页码:24 / 37
页数:14
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