In vitro antiglioma action of indomethacin is mediated via AMP-activated protein kinase/mTOR complex 1 signalling pathway
2017
Аутори:
Pantović, AleksandarBošnjak, Mihajlo
Arsikin, Katarina
Kosić, Milica
Mandić, Miloš
Ristić, Biljana
Tošić, Jelena
Grujičić, Danica
Isaković, Aleksandra
Micic, Nikola
Trajković, Vladimir
Harhaji-Trajković, Ljubica
Тип документа:
Чланак у часопису (Објављена верзија)
,
© 2016 Elsevier Ltd.
Метаподаци
Приказ свих података о документуАпстракт:
We investigated the role of the intracellular energy-sensing AMP-activated protein kinase (AMPK)/mammalian target of rapamycin (mTOR) pathway in the in vitro antiglioma effect of the cyclooxygenase (COX) inhibitor indomethacin. Indomethacin was more potent than COX inhibitors diclofenac, naproxen, and ketoprofen in reducing the viability of U251 human glioma cells. Antiglioma effect of the drug was associated with p21 increase and G2M cell cycle arrest, as well as with oxidative stress, mitochondrial depolarization, caspase activation, and the induction of apoptosis. Indomethacin increased the phosphorylation of AMPK and its targets Raptor and acetyl-CoA carboxylase (ACC), and reduced the phosphorylation of mTOR and mTOR complex 1 (mTORC1) substrates p70S6 kinase and PRAS40 (Ser183). AMPK knockdown by RNA interference, as well as the treatment with the mTORC1 activator leucine, prevented indomethacin-mediated mTORC1 inhibition and cytotoxic action, while AMPK activators metformin and AICAR mimicked the effects of the drug. AMPK activation by indomethacin correlated with intracellular ATP depletion and increase in AMP/ATP ratio, and was apparently independent of COX inhibition or the increase in intracellular calcium. Finally, the toxicity of indomethacin towards primary human glioma cells was associated with the activation of AMPK/Raptor/ACC and subsequent suppression of mTORC1/S6K. By demonstrating the involvement of AMPK/mTORC1 pathway in the antiglioma action of indomethacin, our results support its further exploration in glioma therapy.
Кључне речи:
Indomethacin; Glioma; Apoptosis; AMPK; mTORИзвор:
The International Journal of Biochemistry & Cell Biology, 2017, 83, 84-96Финансирање / пројекти:
- Улога аутофагије у регулацији смрти туморских ћелија (RS-MESTD-Basic Research (BR or ON)-173053)
- Модулација сигналних путева који контролишу интрацелуларни енергетски баланс у терапији тумора и неуро-имуно-ендокриних поремећаја (RS-MESTD-Integrated and Interdisciplinary Research (IIR or III)-41025)
DOI: 10.1016/j.biocel.2016.12.007
ISSN: 1357-2725
PubMed: 27988363
WoS: 000394192400010
Scopus: 2-s2.0-85008690027
URI
http://linkinghub.elsevier.com/retrieve/pii/S1357272516303946https://www.scopus.com/record/display.uri?eid=2-s2.0-85008690027&origin=SingleRecordEmailAlert&dgcid=scalert_sc_search_email&txGid=BCBFF82A73D51FA0ED62BC41FE5E5987.wsnAw8kcdt7IPYLO0V48gA%3A29
https://radar.ibiss.bg.ac.rs/handle/123456789/2512