دورية أكاديمية

Assessing the mechanism and therapeutic potential of modulators of the human Mediator complex-associated protein kinases

التفاصيل البيبلوغرافية
العنوان: Assessing the mechanism and therapeutic potential of modulators of the human Mediator complex-associated protein kinases
المؤلفون: Clarke, Paul A., Ortiz-Ruiz, Maria-Jesus, TePoele, Robert, Adeniji-Popoola, Olajumoke, Box, Gary, Court, Will, Czasch, Stefanie, El Bawab, Samer, Esdar, Christina, Ewan, Ken, Gowan, Sharon, De Haven Brandon, Alexis, Hewitt, Phllip, Hobbs, Stephen M., Kaufmann, Wolfgang, Mallinger, Aurélie, Raynaud, Florence, Roe, Toby, Rohdich, Felix, Schiemann, Kai, Simon, Stephanie, Schneider, Richard, Valenti, Melanie, Weigt, Stefan, Blagg, Julian, Blaukat, Andree, Dale, Trevor C., Eccles, Suzanne A., Hecht, Stefan, Urbahns, Klaus, Workman, Paul, Wienke, Dirk
بيانات النشر: eLife Sciences Publications
سنة النشر: 2016
المجموعة: Cardiff University: ORCA (Online Research @ Cardiff)
الوصف: Mediator-associated kinases CDK8/19 are context-dependent drivers or suppressors of tumorigenesis. Their inhibition is predicted to have pleiotropic effects, but it is unclear whether this will impact on the clinical utility of CDK8/19 inhibitors. We discovered two series of potent chemical probes with high selectivity for CDK8/19. Despite pharmacodynamic evidence for robust on-target activity, the compounds exhibited modest, though significant, efficacy against human tumor lines and patient-derived xenografts. Altered gene expression was consistent with CDK8/19 inhibition, including profiles associated with super-enhancers, immune and inflammatory responses and stem cell function. In a mouse model expressing oncogenic beta-catenin, treatment shifted cells within hyperplastic intestinal crypts from a stem cell to a transit amplifying phenotype. In two species, neither probe was tolerated at therapeutically-relevant exposures. The complex nature of the toxicity observed with two structurally-differentiated chemical series is consistent with ontarget effects posing significant challenges to the clinical development of CDK8/19 inhibitors.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: https://orca.cardiff.ac.uk/id/eprint/96966/1/elife-20722-v3.pdfTest; Clarke, Paul A., Ortiz-Ruiz, Maria-Jesus, TePoele, Robert, Adeniji-Popoola, Olajumoke, Box, Gary, Court, Will, Czasch, Stefanie, El Bawab, Samer, Esdar, Christina, Ewan, Ken orcid:0000-0001-6622-9009 orcid:0000-0001-6622-9009, Gowan, Sharon, De Haven Brandon, Alexis, Hewitt, Phllip, Hobbs, Stephen M., Kaufmann, Wolfgang, Mallinger, Aurélie, Raynaud, Florence, Roe, Toby, Rohdich, Felix, Schiemann, Kai, Simon, Stephanie, Schneider, Richard, Valenti, Melanie, Weigt, Stefan, Blagg, Julian, Blaukat, Andree, Dale, Trevor C. https://orca.cardiff.ac.uk/view/cardiffauthors/A050728Q.htmlTest orcid:0000-0002-4880-9963 orcid:0000-0002-4880-9963, Eccles, Suzanne A., Hecht, Stefan, Urbahns, Klaus, Workman, Paul and Wienke, Dirk 2016. Assessing the mechanism and therapeutic potential of modulators of the human Mediator complex-associated protein kinases. eLife 5 , e20722. 10.7554/eLife.20722 https://doi.org/10.7554/eLife.20722Test file https://orca.cardiff.ac.uk/id/eprint/96966/1/elife-20722-v3.pdfTest
DOI: 10.7554/eLife.20722
الإتاحة: https://doi.org/10.7554/eLife.20722Test
https://orca.cardiff.ac.uk/id/eprint/96966Test/
https://orca.cardiff.ac.uk/id/eprint/96966/1/elife-20722-v3.pdfTest
حقوق: cc_by
رقم الانضمام: edsbas.CDE940CB
قاعدة البيانات: BASE