Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/27756
Title: New derivatives of lupane triterpenoids disturb breast cancer mitochondria and induce cell death
Authors: Serafim, Teresa L. 
Carvalho, Filipa S. 
Bernardo, Telma C. 
Pereira, Gonçalo C. 
Perkins, Edward 
Holy, Jon 
Krasutsky, Dmytro A. 
Kolomitsyna, Oksana N. 
Krasutsky, Pavel A. 
Oliveira, Paulo J. 
Keywords: Bioenergetics; Breast cancer; Cell death; Cytotoxicity; Lupane triterpenoids derivatives; Mitochondrial physiology
Issue Date: 1-Nov-2014
Publisher: Elsevier
Citation: SERAFIM, Teresa L. [et. al] - New derivatives of lupane triterpenoids disturb breast cancer mitochondria and induce cell death. "Bioorganic & Medicinal Chemistry". ISSN 0968-0896. Vol. 22 Nº. 21 (2014) p. 6270–6287
Serial title, monograph or event: Bioorganic & Medicinal Chemistry
Volume: 22
Issue: 21
Abstract: Novel cationic dimethylaminopyridine derivatives of pentacyclic triterpenes were previously described to promote mitochondrial depolarization and cell death in breast and melanoma cell lines. The objective of this work was to further investigate in detail the mechanism of mitochondrial perturbations, correlating those effects with breast cancer cell responses to those same agents. Initially, a panel of tumor and non-tumor cell lines was grown in high-glucose or glucose-free glutamine-containing media, the later forcing cells to synthesize ATP by oxidative phosphorylation only. Cell proliferation, cell cycle, cell death and mitochondrial membrane polarization were evaluated. Inhibition of cell proliferation was observed, accompanied by an arrest in the G1-cell cycle phase, and importantly, by loss of mitochondrial membrane potential. On a later time-point, caspase-9 and 3 activation were observed, resulting in cell death. For the majority of test compounds, we determined that cell toxicity was augmented in the galactose media. To investigate direct evidences on mitochondria isolated rat liver mitochondria were used. The results showed that the compounds were strong inducers of the permeability transition pore. Confirming our previous results, this work shows that the novel DMAP derivatives strongly interact with mitochondria, resulting in pro-apoptotic signaling and cell death.
URI: http://hdl.handle.net/10316/27756
ISSN: 0968-0896
DOI: 10.1016/j.bmc.2014.08.013
Rights: openAccess
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
FCTUC Ciências da Vida - Artigos em Revistas Internacionais

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