Carfilzomib Enhances the Suppressive Effect of Ruxolitinib in Myelofibrosis.

carfilzomib myelofibrosis ruxolitinib shRNA library screen

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
28 Sep 2021
Historique:
received: 30 08 2021
revised: 17 09 2021
accepted: 20 09 2021
entrez: 13 10 2021
pubmed: 14 10 2021
medline: 14 10 2021
Statut: epublish

Résumé

As the first FDA-approved tyrosine kinase inhibitor for treatment of patients with myelofibrosis (MF), ruxolitinib improves clinical symptoms but does not lead to eradication of the disease or significant reduction of the mutated allele burden. The resistance of MF clones against the suppressive action of ruxolitinib may be due to intrinsic or extrinsic mechanisms leading to activity of additional pro-survival genes or signalling pathways that function independently of JAK2/STAT5. To identify alternative therapeutic targets, we applied a pooled-shRNA library targeting ~5000 genes to a

Identifiants

pubmed: 34638347
pii: cancers13194863
doi: 10.3390/cancers13194863
pmc: PMC8507927
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Kay Kendall Leukaemia Fund
ID : KKL1072

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Auteurs

Simone Claudiani (S)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Clinton C Mason (CC)

Department of Pediatrics, Division of Pediatric Hematology and Oncology, University of Utah, Salt Lake City, UT 84108, USA.

Dragana Milojkovic (D)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Andrea Bianchi (A)

Department of Information Engineering, University of L'Aquila, 67100 L'Aquila, Italy.

Cristina Pellegrini (C)

Department of Biotechnological and Applied Clinical Science, University of L'Aquila, 67100 L'Aquila, Italy.

Antinisca Di Marco (A)

Department of Information Engineering, University of L'Aquila, 67100 L'Aquila, Italy.

Carme R Fiol (CR)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Mark Robinson (M)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Kanagaraju Ponnusamy (K)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Katya Mokretar (K)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Avirup Chowdhury (A)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Michael Albert (M)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Alistair G Reid (AG)

Molecular Pathology Unit, Liverpool University, Liverpool L7 8XP, UK.

Michael W Deininger (MW)

Versiti Blood Research Institute, Division of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

Kikkeri Naresh (K)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Jane F Apperley (JF)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Jamshid S Khorashad (JS)

Centre for Haematology, Department of Immunology and Inflammation, Imperial College, London W12 0NN, UK.

Classifications MeSH