Oxygen-Dependent Interactions between the Ruthenium Cage and the Photoreleased Inhibitor in NAMPT-Targeted Photoactivated Chemotherapy.
Selda AbyarLuojiao HuangYurii HusievLudovic BretinBobby ChauVadde RamuJacob Hendricus WildemanKimberley BelforLukas S WijayaVera E van der NoordAmy C HarmsMaxime A SieglerSylvia E Le DévédecSylvestre A BonnetPublished in: Journal of medicinal chemistry (2024)
Photoactivated chemotherapy agents form a new branch of physically targeted anticancer agents with potentially lower systemic side effects for patients. On the other hand, limited information exists on the intracellular interactions between the photoreleased metal cage and the photoreleased anticancer inhibitor. In this work, we report a new biological study of the known photoactivated compound Ru-STF31 in the glioblastoma cancer cell line, U87MG. Ru-STF31 targets nicotinamide phosphoribosyltransferase (NAMPT), an enzyme overexpressed in U87MG. Ru-STF31 is activated by red light irradiation and releases two photoproducts: the ruthenium cage and the cytotoxic inhibitor STF31 . This study shows that Ru-STF31 can significantly decrease intracellular NAD + levels in both normoxic (21% O 2 ) and hypoxic (1% O 2 ) U87MG cells. Strikingly, NAD + depletion by light activation of Ru-STF31 in hypoxic U87MG cells could not be rescued by the addition of extracellular NAD + . Our data suggest an oxygen-dependent active role of the ruthenium photocage released by light activation.
Keyphrases
- induced apoptosis
- energy transfer
- end stage renal disease
- newly diagnosed
- endoplasmic reticulum stress
- ejection fraction
- cancer therapy
- locally advanced
- healthcare
- squamous cell carcinoma
- prognostic factors
- cell death
- drug delivery
- young adults
- patient reported outcomes
- artificial intelligence
- cell proliferation
- quantum dots
- drug induced