Applications of phototherapies for the management of skin cancer along with their mechanism of action
No. | Source of light (phototherapy) | Target | Treatment of skin cancer | Mechanism of action | References |
---|---|---|---|---|---|
1 | PUVA | Psoralen and DNA | Skin mastocytosis and cutaneous T-cell lymphoma | Apoptosis, cell cycle arrest, reactive oxygen species (ROS) production, and DNA replication inhibition | [119] |
2 | UVA1 (340–400 nm) | Chromophores | Atopic dermatitis, localized scleroderma | T-cell apoptosis and tissue remodeling | [120] |
3 | PDT | Photosensitizers | Superficial skin cancer | Apoptosis and ROS production | [121] |
4 | Ablation [CO2 laser (10,800 nm); erbium:yttrium aluminum garnet laser (Er:YAG laser, 3,850 nm)] | Water in and outside the cells | Superficial skin cancer | Evaporation | [122] |
5 | Non-ablation (dye laser) | Hemoglobin (Hb) | Telangiectasia, vascular lesions, as well as hemangioma | Photoselective thermolysis | [123] |
6 | Extra-corporeal photopheresis | Chromophore | Erythrodermic cutaneous T-cell lymphoma | T-cells depletion | [124] |
Authors would like to offer special thanks to MM College of Pharmacy, Amity institute of Nanotechnology for allowing carrying out this work and other research projects.
RG, SH, and KW: Writing—original draft, Writing—review & editing, Visualization. HC: Supervision, Investigation, Conceptualization, Writing—review & editing. RP: Formal analysis, Resources, Visualization. ML and RS: Writing—review & editing, Supervision, Methodology. All the authors have equally contributed to conceiving this paper and participated in its revisions. All authors read and approved the final manuscript.
The authors have no relevant conflicts of interest.
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© The Author(s) 2023.