Direkt zum Inhalt
Merck

Discovering chemical modifiers of oncogene-regulated hematopoietic differentiation.

Nature chemical biology (2009-01-28)
Jing-Ruey J Yeh, Kathleen M Munson, Kamaleldin E Elagib, Adam N Goldfarb, David A Sweetser, Randall T Peterson
ZUSAMMENFASSUNG

It has been proposed that inhibitors of an oncogene's effects on multipotent hematopoietic progenitor cell differentiation may change the properties of the leukemic stem cells and complement the clinical use of cytotoxic drugs. Using zebrafish, we developed a robust in vivo hematopoietic differentiation assay that reflects the activity of the oncogene AML1-ETO. Screening for modifiers of AML1-ETO-mediated hematopoietic dysregulation uncovered unexpected roles of COX-2- and beta-catenin-dependent pathways in AML1-ETO function. This approach may open doors for developing therapeutics targeting oncogene function within leukemic stem cells.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Actidion, from microbial, ≥94% (TLC)
Sigma-Aldrich
Cycloheximid -Lösung, Ready-Made Solution, microbial, 100 mg/mL in DMSO, Suitable for cell culture
Sigma-Aldrich
Rotenon, ≥95%
Sigma-Aldrich
Indomethacin, 98.0-102.0%, meets EP testing specifications
Sigma-Aldrich
Prostaglandin E2, synthetic, powder, BioReagent, suitable for cell culture
Sigma-Aldrich
Actidion, Biotechnology Performance Certified
Sigma-Aldrich
Prostaglandin E2, γ-irradiated, powder, BioXtra, suitable for cell culture
Sigma-Aldrich
Prostaglandin E2, ≥93% (HPLC), synthetic
Sigma-Aldrich
Indomethacin, meets USP testing specifications
Supelco
Rotenon, PESTANAL®, analytical standard
Supelco
Actidion, PESTANAL®, analytical standard
Sigma-Aldrich
Bis(5-chlor-2-hydroxyphenyl)methan, 95%