Rationale for a Combination Therapy with the STAT5 Inhibitor AC-4-130 and the MCL1 Inhibitor S63845 in the Treatment of FLT3-Mutated or TET2-Mutated Acute Myeloid Leukemia.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
28 Jul 2021
Historique:
received: 28 05 2021
revised: 19 07 2021
accepted: 26 07 2021
entrez: 7 8 2021
pubmed: 8 8 2021
medline: 15 9 2021
Statut: epublish

Résumé

The FMS-like tyrosine kinase 3 (

Identifiants

pubmed: 34360855
pii: ijms22158092
doi: 10.3390/ijms22158092
pmc: PMC8347059
pii:
doi:

Substances chimiques

DNA-Binding Proteins 0
Proto-Oncogene Proteins 0
Pyrimidines 0
S63845 0
STAT5 Transcription Factor 0
STAT5A protein, human 0
Thiophenes 0
Tumor Suppressor Proteins 0
Dioxygenases EC 1.13.11.-
TET2 protein, human EC 1.13.11.-
FLT3 protein, human EC 2.7.10.1
fms-Like Tyrosine Kinase 3 EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
ID : #310030_127509

Références

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Auteurs

Katja Seipel (K)

Department for Biomedical Research, University of Bern, 2008 Bern, Switzerland.

Carolyn Graber (C)

Department for Biomedical Research, University of Bern, 2008 Bern, Switzerland.

Laura Flückiger (L)

Department for Biomedical Research, University of Bern, 2008 Bern, Switzerland.

Ulrike Bacher (U)

Department of Hematology, University Hospital Bern, 3010 Bern, Switzerland.

Thomas Pabst (T)

Department of Medical Oncology, University Hospital Bern, 3010 Bern, Switzerland.

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Classifications MeSH