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Review
. 2022;26(1):1-7.
doi: 10.5114/wo.2021.112447. Epub 2022 Feb 4.

Oxidative stress in melanogenesis and melanoma development

Affiliations
Review

Oxidative stress in melanogenesis and melanoma development

Kacper Kamiński et al. Contemp Oncol (Pozn). 2022.

Abstract

Melanoma is the most aggressive skin cancer, with a growing number of incidents worldwide and with no effective cure in a metastatic stage so far. There are several pathways and processes engaged in melanoma pathogenesis that have been extensively explored in recent years. The emerging evidence suggests that oxidative stress (OS) is highly involved in melanin synthesis and melanoma formation. Melanoma is particularly susceptible to OS due to the involvement of melanin synthesis and UV radiation in the generation of reactive oxygen species. Oxidative stress influences melanoma immunity, the metastatic potential of melanoma cells and their resistance to therapy. In malignant melanocytes, the process of melanogenesis is frequently upregulated, suggesting possible therapeutic targets. This review describes the role of OS in melanin synthesis in melanocytes and explains how it affects melanoma cells. Better knowledge about the mechanisms involved in cancer progression may result in the development of better treatment strategies.

Keywords: melanogenesis; melanoma; oxidative stress.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Fig. 1
Fig. 1
Schematic representation of melanogenesis pathway in humans
Fig. 2
Fig. 2
Heatmap of correlations between three of the gene members of melanogenesis and nineteen genes representing oxidative stress pathway in melanoma patients (n = 444); p-value < 0.05 was considered significant

References

    1. Liu-Smith F, Dellinger R, Meyskens FL Jr. Updates of reactive oxygen species in melanoma etiology and progression. Arch Biochem Biophys 2014; 563: 51-55. - PMC - PubMed
    1. Finkel T. Signal transduction by reactive oxygen species. J Cell Biol 2011; 194: 7-15. - PMC - PubMed
    1. Negri S, Faris P, Moccia F. Reactive oxygen species and endothelial Ca2+ signaling: brothers in arms or partners in crime? Int J Mol Sci 2021; 22: 9821. - PMC - PubMed
    1. Kumari S, Guan Thng ST, Kumar Verma N, Gautam HK. Melanogenesis inhibitors. Acta Derm Venereol 2018; 98: 924-931. - PubMed
    1. D’Mello SAN, Finlay GJ, Baguley BC, Askarian-Amiri ME. Signaling pathways in melanogenesis. Int J Mol Sci 2016; 17: 1144. - PMC - PubMed