Ursolic Acid Inhibits Collective Cell Migration and Promotes JNK-Dependent Lysosomal Associated Cell Death in Glioblastoma Multiforme Cells
Autor: | Carlos Barcia, Gillian E. Conway, Deimante Zizyte, James F. Curtin, Lorna Lynam, Julie Rose Mae Mondala, Orla Howe, Mathilde Lecourt, Zhonglei He |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Programmed cell death lcsh:Medicine lcsh:RS1-441 Pharmaceutical Science ursolic acid migration Article law.invention Flow cytometry lcsh:Pharmacy and materia medica 03 medical and health sciences chemistry.chemical_compound lysosomes 0302 clinical medicine Ursolic acid Confocal microscopy law Drug Discovery Organelle Medicine and Health Sciences medicine Cytotoxic T cell Cytotoxicity nutraceuticals medicine.diagnostic_test Chemistry lcsh:R Autophagy nervous system diseases Cell biology cell death 030104 developmental biology 030220 oncology & carcinogenesis Molecular Medicine |
Zdroj: | Pharmaceuticals, Vol 14, Iss 91, p 91 (2021) Pharmaceuticals Volume 14 Issue 2 Articles |
ISSN: | 1424-8247 |
Popis: | Ursolic acid (UA) is a bioactive compound which has demonstrated therapeutic efficacy in a variety of cancer cell lines. UA activates various signalling pathways in Glioblastoma multiforme (GBM) and offers a promising starting point in drug discovery however, understanding the relationship between cell death and migration has yet to be elucidated. UA induces a dose dependent cytotoxic response demonstrated by flow cytometry and biochemical cytotoxicity assays. Inhibitor and fluorescent probe studies demonstrate that UA induces a caspase independent, JNK dependent, mechanism of cell death. Migration studies established that UA inhibits GBM collective cell migration in a time dependent manner that is independent of the JNK signalling pathway. Cytotoxicity induced by UA results in the formation of acidic vesicle organelles (AVOs), speculating the activation of autophagy. However, inhibitor and spectrophotometric analysis demonstrated that autophagy was not responsible for the formation of the AVOs. Confocal microscopy and isosurface visualisation determined co-localisation of lysosomes with the previously identified AVOs, thus providing evidence that lysosomes are likely to be playing a role in UA induced cell death. Collectively, our data identify that UA rapidly induces a lysosomal associated mechanism of cell death in addition to UA acting as an inhibitor of GBM collective cell migration. |
Databáze: | OpenAIRE |
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