Highly variable biological effects of statins on cancer, non-cancer, and stem cells in vitro

. 2024 May 23 ; 14 (1) : 11830. [epub] 20240523

Jazyk angličtina Země Velká Británie, Anglie Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid38782983

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

Odkazy

PubMed 38782983
PubMed Central PMC11116523
DOI 10.1038/s41598-024-62615-w
PII: 10.1038/s41598-024-62615-w
Knihovny.cz E-zdroje

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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