Literature DB >> 16193102

JAK protein kinase inhibitors.

James E Thompson1.   

Abstract

In humans, the Janus protein tyrosine kinase family (JAKs) contains four members: JAK1, JAK2, JAK3 and TYK2. JAKs phosphorylate signal transducers and activators of transcription (STATs) simultaneously with other phosphorylations required for activation, and there are several cellular mechanisms in place to inhibit JAK/STAT signaling. That one might be able to modulate selected JAK/STAT-mediated cellular signals by inhibiting JAK kinase activity to effect a positive therapeutic outcome is a tantalizing prospect, as yet incompletely realized. While current data suggest no therapeutic use for JAK1 and TYK2 inhibition, JAK2 inhibition seems a promising but not definitively tested mechanism for treatment of leukemia. More promising, however, are data indicating a possible therapeutic use of JAK3 inhibition. The restriction of the JAK3-deficient phenotype to the hematopoietic system and the resulting profound immune suppression suggest that JAK3 could be a target for immunosuppressive therapies used to prevent organ transplant rejection.

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Year:  2005        PMID: 16193102     DOI: 10.1358/dnp.2005.18.5.904198

Source DB:  PubMed          Journal:  Drug News Perspect        ISSN: 0214-0934


  5 in total

1.  Modulation of activation-loop phosphorylation by JAK inhibitors is binding mode dependent.

Authors:  Rita Andraos; Zhiyan Qian; Débora Bonenfant; Joëlle Rubert; Eric Vangrevelinghe; Clemens Scheufler; Fanny Marque; Catherine H Régnier; Alain De Pover; Hugues Ryckelynck; Neha Bhagwat; Priya Koppikar; Aviva Goel; Lorenza Wyder; Gisele Tavares; Fabienne Baffert; Carole Pissot-Soldermann; Paul W Manley; Christoph Gaul; Hans Voshol; Ross L Levine; William R Sellers; Francesco Hofmann; Thomas Radimerski
Journal:  Cancer Discov       Date:  2012-05-03       Impact factor: 39.397

2.  Tricyclic covalent inhibitors selectively target Jak3 through an active site thiol.

Authors:  Eric R Goedken; Maria A Argiriadi; David L Banach; Bryan A Fiamengo; Sage E Foley; Kristine E Frank; Jonathan S George; Christopher M Harris; Adrian D Hobson; David C Ihle; Douglas Marcotte; Philip J Merta; Mark E Michalak; Sara E Murdock; Medha J Tomlinson; Jeffrey W Voss
Journal:  J Biol Chem       Date:  2014-12-31       Impact factor: 5.157

Review 3.  Tofacitinab in renal transplantation.

Authors:  Martin S Zand
Journal:  Transplant Rev (Orlando)       Date:  2013-07       Impact factor: 3.943

4.  Annexin A1 released from apoptotic cells acts through formyl peptide receptors to dampen inflammatory monocyte activation via JAK/STAT/SOCS signalling.

Authors:  Danute Pupjalis; Julia Goetsch; Diane J Kottas; Volker Gerke; Ursula Rescher
Journal:  EMBO Mol Med       Date:  2011-01-20       Impact factor: 12.137

5.  Stat3 is tyrosine-phosphorylated through the interleukin-6/glycoprotein 130/Janus kinase pathway in breast cancer.

Authors:  Marjan Berishaj; Sizhi Paul Gao; Simi Ahmed; Kenneth Leslie; Hikmat Al-Ahmadie; William L Gerald; William Bornmann; Jacqueline F Bromberg
Journal:  Breast Cancer Res       Date:  2007       Impact factor: 6.466

  5 in total

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