Target-Based Small Molecule Drug Discovery Towards Novel Therapeutics for Inflammatory Bowel Diseases

被引:21
|
作者
Li, Yi [1 ]
Chen, Jianping [1 ]
Bolinger, Andrew A. [1 ]
Chen, Haiying [1 ]
Liu, Zhiqing [1 ]
Cong, Yingzi [3 ]
Brasier, Allan R. [4 ]
Pinchuk, Irina, V [5 ]
Tian, Bing [2 ]
Zhou, Jia [1 ]
机构
[1] Univ Texas Med Branch, Dept Pharmacol & Toxicol, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Dept Internal Med, Galveston, TX 77555 USA
[3] Univ Texas Med Branch, Dept Microbiol & Immunol, Galveston, TX 77555 USA
[4] Univ Wisconsin, Inst Clin & Translat Res ICTR, Madison, WI 53705 USA
[5] Penn State Hlth Milton S Hershey Med Ctr, Dept Med, Hershey, PA 17033 USA
关键词
inflammatory bowel disease (IBD); ulcerative colitis (UC); Crohn's disease (CD); drug targets and signaling pathways; drug discovery and development; therapeutics; JANUS KINASE INHIBITOR; CHEMOKINE RECEPTOR 9; SELECTIVE JAK1 INHIBITOR; CELL-ADHESION MOLECULE-1; NLRP3; INFLAMMASOME; ULCERATIVE-COLITIS; INTESTINAL INFLAMMATION; MAINTENANCE THERAPY; CROHNS-DISEASE; TRANSCRIPTIONAL ELONGATION;
D O I
10.1093/ibd/izab190
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Inflammatory bowel disease (IBD), including ulcerative colitis (UC) and Crohn's disease (CD), is a class of severe and chronic diseases of the gastrointestinal (GI) tract with recurrent symptoms and significant morbidity. Long-term persistence of chronic inflammation in IBD is a major contributing factor to neoplastic transformation and the development of colitis-associated colorectal cancer. Conversely, persistence of transmural inflammation in CD is associated with formation of fibrosing strictures, resulting in substantial morbidity. The recent introduction of biological response modifiers as IBD therapies, such as antibodies neutralizing tumor necrosis factor (TNF)-alpha, have replaced nonselective anti-inflammatory corticosteroids in disease management. However, a large proportion (similar to 40%) of patients with the treatment of anti-TNF-alpha antibodies are discontinued or withdrawn from therapy because of (1) primary nonresponse, (2) secondary loss of response, (3) opportunistic infection, or (4) onset of cancer. Therefore, the development of novel and effective therapeutics targeting specific signaling pathways in the pathogenesis of IBD is urgently needed. In this comprehensive review, we summarize the recent advances in drug discovery of new small molecules in preclinical or clinical development for treating IBD that target biologically relevant pathways in mucosal inflammation. These include intracellular enzymes (Janus kinases, receptor interacting protein, phosphodiesterase 4, I kappa B kinase), integrins, G protein-coupled receptors (S1P, CCR9, CXCR4, CB2) and inflammasome mediators (NLRP3), etc. We will also discuss emerging evidence of a distinct mechanism of action, bromodomain-containing protein 4, an epigenetic regulator of pathways involved in the activation, communication, and trafficking of immune cells. We highlight their chemotypes, mode of actions, structure-activity relationships, characterizations, and their in vitro/in vivo activities and therapeutic potential. The perspectives on the relevant challenges, new opportunities, and future directions in this field are also discussed.
引用
收藏
页码:S38 / S62
页数:25
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