Differentiation of HL-60 myeloid leukemia cells induced by all-trans retinoic acid is enhanced in combination with caffeic acid
Jazyk angličtina Země Řecko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
15254783
Knihovny.cz E-zdroje
- MeSH
- akutní promyelocytární leukemie farmakoterapie MeSH
- antigeny nádorové biosyntéza MeSH
- barvicí látky farmakologie MeSH
- buněčná diferenciace MeSH
- časové faktory MeSH
- CD antigeny MeSH
- chemické modely MeSH
- GPI-vázané proteiny MeSH
- HL-60 buňky MeSH
- imunofenotypizace MeSH
- kyseliny kávové aplikace a dávkování chemie MeSH
- lidé MeSH
- molekuly buněčné adheze biosyntéza MeSH
- proliferace buněk MeSH
- protokoly antitumorózní kombinované chemoterapie terapeutické užití MeSH
- průtoková cytometrie MeSH
- synergismus léků * MeSH
- tetrazoliové soli farmakologie MeSH
- thiazoly farmakologie MeSH
- tretinoin aplikace a dávkování MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigeny nádorové MeSH
- barvicí látky MeSH
- caffeic acid MeSH Prohlížeč
- CD antigeny MeSH
- CEACAM8 protein, human MeSH Prohlížeč
- GPI-vázané proteiny MeSH
- kyseliny kávové MeSH
- molekuly buněčné adheze MeSH
- tetrazoliové soli MeSH
- thiazoly MeSH
- thiazolyl blue MeSH Prohlížeč
- tretinoin MeSH
We investigated a possible enhancement of all-trans retinoic acid (ATRA)-induced differentiation of HL-60 human myeloid leukemia cells by caffeic acid (CA), a widely distributed plant phenolic compound. Our results showed that CA, in the concentration of 13 or 52 micro M, had no or minimal influence on cell differentiation, whereas the differentiating activity of ATRA was potentiated by CA treatment. We proved, using flow cytometric detection of the CD66b surface molecule, a synergistic effect of CA: at day 10, 18.3% of CD66b-positive cells were detected after treatment with ATRA only, and 33% when CA and ATRA were combined together. NBT-assay confirmed that this additive effect of CA on ATRA-induced differentiation. Proliferating activity as assessed by MTT-assay was generally not affected by CA at given concentrations. However, cell proliferation was significantly reduced by 52 micro M CA at 96-h intervals. This effect was markedly enhanced when CA, at both concentrations, and ATRA were combined. The possibility to enhance the differentiation potential of ATRA by CA may improve outcomes in the therapy of acute promyelocytic leukemia.
Why Differentiation Therapy Sometimes Fails: Molecular Mechanisms of Resistance to Retinoids