Highly variable biological effects of statins on cancer, non-cancer, and stem cells in vitro
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
APVV-15-0217
Slovak Research and Development Agency
VEGA-1/0405/22
Ministry of Education, Research, Development and Youth of the Slovak Republic
CZ.02.1.01/0.0/0.0/16_019/0000785
Operational Programme Research, Development, and Education
MH CZ-DRO-VFN64165
Czech Ministry of Health
PubMed
38782983
PubMed Central
PMC11116523
DOI
10.1038/s41598-024-62615-w
PII: 10.1038/s41598-024-62615-w
Knihovny.cz E-zdroje
- Klíčová slova
- 3-Hydroxy-3-methylglutaryl coenzyme A inhibitors, Cell spheroids, Microarray analysis, Pancreatic cancer cells, Statins, Stem cells,
- MeSH
- buněčné sféroidy účinky léků MeSH
- HEK293 buňky MeSH
- lidé MeSH
- mezenchymální kmenové buňky * účinky léků metabolismus MeSH
- nádorové buněčné linie MeSH
- nádory slinivky břišní * farmakoterapie patologie metabolismus MeSH
- statiny * farmakologie MeSH
- viabilita buněk * účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- statiny * MeSH
Statins, the drugs used for the treatment of hypercholesterolemia, have come into the spotlight not only as chemoadjuvants, but also as potential stem cell modulators in the context of regenerative therapy. In our study, we compared the in vitro effects of all clinically used statins on the viability of human pancreatic cancer (MiaPaCa-2) cells, non-cancerous human embryonic kidney (HEK 293) cells and adipose-derived mesenchymal stem cells (ADMSC). Additionally, the effect of statins on viability of MiaPaCa-2 and ADMSC cells spheroids was tested. Furthermore, we performed a microarray analysis on ADMSCs treated with individual statins (12 μM) and compared the importance of the effects of statins on gene expression between stem cells and pancreatic cancer cells. Concentrations of statins that significantly affected cancer cells viability (< 40 μM) did not affect stem cells viability after 24 h. Moreover, statins that didn´t affect viability of cancer cells grown in a monolayer, induce the disintegration of cancer cell spheroids. The effect of statins on gene expression was significantly less pronounced in stem cells compared to pancreatic cancer cells. In conclusion, the low efficacy of statins on non-tumor and stem cells at concentrations sufficient for cancer cells growth inhibition, support their applicability in chemoadjuvant tumor therapy.
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