Impact of Aluminium phthalocyanine nanoconjugate on melanoma stem cells.
Bridgette MkhobongoRahul ChandranAbrahamse HeidiPublished in: Artificial cells, nanomedicine, and biotechnology (2023)
Metastatic melanoma cancer stem cells are subpopulations linked to tumour development, immunoevasive behaviour, treatment resistance, and metastasis, all of which contribute to a poor prognosis. Photodynamic treatment (PDT) is an alternate strategy to cancer eradication that involves the generation of reactive oxygen species. As a carrier, nanoparticles enable efficient cellular uptake of photosensitizers, improving organelle accumulation and cancer cell targeted therapy. This study considered at the effect of PDT on CD133 + Melanoma Stem Cells utilising an Aluminium Phthalocyanine Gold Nanoparticle (AlPcS 4 Cl-AuNP) combination. A ligand exchange approach was used to conjugate AlPcS 4 Cl-PEG-AuNP-COOH and was characterised using UV-Vis, FTIR, DLS and Zeta Potential. Stem cells isolated from the A375 cell line irradiated with a laser at 673.2 nm with a fluency of 5 J/cm 2 were evaluated. Furthermore, it was important to study if apoptosis was one of the mechanisms causing to cell death which was substantiated with Annexin V/PI, caspase 3 and p53 analysis. The nanoparticle conjugate mediated PDT promoted apoptotic cell death, showing increased expression of p53 and caspase-3. The study proposed a strategy aimed at extending the understanding of PDT in enhancing the therapy of melanoma, suggesting a probable improved cell death when AlPcS 4 Cl was conjugated to AuNPs.