Anticancer pentamethinium salt is a potent photosensitizer inducing mitochondrial disintegration and apoptosis upon red light illumination
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
32640366
DOI
10.1016/j.jphotobiol.2020.111939
PII: S1011-1344(20)30389-4
Knihovny.cz E-zdroje
- Klíčová slova
- Cancer therapy, Cyanine dyes, Mitochondria, Photodynamic therapy, Photosensitizer, Polymethine compounds,
- MeSH
- apoptóza účinky léků MeSH
- bistrimethylamoniové sloučeniny farmakologie MeSH
- fotochemoterapie MeSH
- fotosenzibilizující látky farmakologie MeSH
- lidé MeSH
- mitochondrie účinky léků fyziologie MeSH
- nádorové buněčné linie MeSH
- reaktivní formy kyslíku metabolismus MeSH
- soli chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- bistrimethylamoniové sloučeniny MeSH
- fotosenzibilizující látky MeSH
- pentamethonium MeSH Prohlížeč
- reaktivní formy kyslíku MeSH
- soli MeSH
Despite progress in the development and application of novel therapeutic agents, cancer remains a major cause of death worldwide. Therefore, there is a need for new approaches to increase therapeutic options and efficiency. The metabolism of cancer cells differs from that of non-malignant cells and their mitochondria show altered activities that can be utilized as a target for drug development. Salt 1 is a low-molecular weight heterocyclic compound of the polymethine class that accumulates in the mitochondria of cancer cells and selectively disrupts their metabolism. Salt 1 leads to a non-apoptotic form of cell death in vitro that is associated with an autophagic cellular response and eventual metabolic collapse, and inhibits human tumor xenograft growth in vivo without apparent toxicity for normal cells. As a pentamethinium compound, salt 1 exhibits intrinsic fluorescence and is a candidate for photosensitization after excitation by appropriate wavelengths of light. Herein, we report that salt 1 is a potent photosensitizer, which generates a photodynamic effect and provides enhanced cytotoxicity compared to salt 1 without light exposure. Importantly, photosensitization is optimally induced by red light, which is used clinically for photosensitization and penetrates further into tissues than lower wavelengths. Cancer cells treated with non-cytotoxic doses of salt 1 and subsequently exposed to 630 nm light show severely damaged mitochondria, manifested by reduced mitochondrial membrane potential and disintegration of the mitochondrial tubular network. As a consequence, cancer cells lose their proliferative potential and die via apoptosis in the presence of light. These findings indicate that salt 1 is a promising photosensitizer with potential to be combined with 630 nm light to strengthen its efficacy in cancer therapy.
Citace poskytuje Crossref.org
Cyanine dyes in the mitochondria-targeting photodynamic and photothermal therapy