Use of endogenous pigment analytes to assess the invasive potential of superficial skin melanomas
https://doi.org/10.24931/2413-9432-2026-15-1-4-10
Abstract
Cutaneous melanoma, which accounts for 72-80% of all diagnosed tumors developing from melanin-producing tissue, is an example of a malignancy whose initiation and development, with rare exceptions, are associated with the realization of endogenous pigmentations in the morphological substrate of the tumor. However, the existing diagnostic paradigm for superficial cutaneous melanomas does not take into account the significance of endogenous pigmentations in assessing the tumor's invasive capacity. This article examines the relationship between changes in the biochemical composition of superficial cutaneous melanomas and their invasive capacity, as well as the possibility of using this relationship in melanoma diagnostics. A comparative pathomorphological, ultrastructural, and spectroscopic study of 128 samples of superficial spreading melanoma removed during radical surgical excision was conducted. A higher frequency and diversity of endogenous pigment analytes were detected during the horizontal phase of tumor growth compared to the vertical phase. Diagnostically significant analytes included carotenoid pigments (p=0.02257), porphyrin (p=0.09080), and melanin precursors tyrosine (p=0.01554) and phenylalanine (p=0.01753). The use of a comprehensive pathomorphological and spectroscopic study and multiplex analysis of the obtained results made it possible to simultaneously identify a significant number of statistically confirmed endogenous pigment analytes in superficial melanoma skin samples. These analytes have diagnostic value in assessing the invasive capacity of superficial melanomas.
About the Authors
A. V. BorisovRussian Federation
Tyumen
I. A. Chernov
Russian Federation
Tyumen
A. M. Avdalyan
Russian Federation
Moscow
S. E. Timofeev
Russian Federation
Moscow
A. V. Ronzin
Russian Federation
Moscow
A. I. Nichiporov
Russian Federation
Moscow
V. I. Kukushkin
Russian Federation
Chernogolovka
Yu. A. Kirillov
Russian Federation
Tyumen
Moscow
References
1. Shakhzadova A.O., Starinsky V.V., Lisichnikova I.V. The state of cancer care for the population of Russia in 2022. Siberian Journal of Oncology, 2023, Vol. 22 (5), pp. 5-13. doi:10.21294/1814-4861-2023-22-5-5-13
2. Siegel R.L., Miller K.D., Jemal A. Cancer statistics. A Cancer Journal for Clinicians, 2020, Vol. 70(1), pp. 7-30. doi:10.3322/caac.21590.
3. Ostrowski S.M., Fisher D.E. Biology of melanoma. Hematology/ Oncology Clinics of North America, 2021, Vol. 35(1), pp. 29-56. doi:10.1016/j.hoc.2020.08.010.
4. Namikawa K., Yamazaki N. Targeted Therapy and Immunotherapy for Melanoma in Japan. Current Treatment Options in Oncology, 2019, Vol. 20(1). doi:10.1007/s11864-019-0607-8.
5. Mao L., Qi Z., Zhang L., Guo J., Si L. Immunotherapy in Acral and Mucosal Melanoma: Current Status and Future Directions. Frontiers in immunology, 2021, Vol. 12, pp. 1-13. doi:10.3389/fimmu.2021.680407.eCollection 2021.
6. Reynolds E.S. The use of lead citrate at high pH as an electronopaque stain in electron microscopy. Journal of Cell Biology, 1963, Vol. 17(1), pp. 208-212. doi:10.1083/jcb.17.1.208
7. Friedman R.J., Rigel D.S., Kopf A.W. Early detection of malignant melanoma: the role of physician examination and selfexamination of the skin. A Cancer Journal for Clinicians, 1985, Vol. 35(3), pp. 130-151. doi:10.3322/canjclin.35.3.130.
8. Pavri S.N., Clune J., Ariyan S., Narayan D. Malignant Melanoma: Beyond the Basics.PlastReconstrSurg, 2016, Vol. 138(2), pp. 330- 340. doi:10.1097/PRS.0000000000002367.
9. Bobos M. Histopathologic classification and prognostic factors of melanoma: a 2021 update. Italian Journal of Dermatology and Venereology, 2021, Vol. 156, no. 3, pp. 300-321. doi:10.23736/S2784-8671.21.06958-3.
10. Tsolekile N., Nelana S., Oluwafemi O.S. Porphyrin as Diagnostic and Therapeutic Agent. Molecules, 2019, Vol. 24(14), pp. 2669 doi:10.3390/molecules24142669.
11. Nishida K., Tojo T., Kondo T., Yuasa M. Evaluation of the correlation between porphyrin accumulation in cancer cells and functional positions for application as a drug carrier. Scientific Reports, 2021, Vol. 11(1), pp. 2046. doi:10.1038/s41598-021-81725-3.
12. Yang F., Xu M., Chen X., Luo Y. Spotlight on porphyrins: Classifications, mechanisms and medical applications. Biomedicine & Pharmacotherapy, 2023, vol. 164, pp. 114933. doi:10.1016/j.biopha.2023.114933.
13. Virchow R. Die krankheiten Geschwiulste. Course taught at the University of Berlin , 1863, Vol. 24, pp. 369-434.
14. Medori M.C., Donato K., Dhuli K., Maltese P.E., Tanzi B., Tezzele S., Mareso C., Miertus J., Generali D. et al. Omics sciences and precision medicine in melanoma. Clinica terapeutica, 2023, Vol. 174, suppl. 2(6), pp. 29-36. doi:10.7417/CT.2023.2469.
15. Routy B., Jackson T., Mählmann L., Baumgartner C.K., Blaser M., Byrd A., Corvaia N., Couts K., Davar D., Derosa L. et al. Melanoma and microbiota: Current understanding and future directions. Cancer
Review
For citations:
Borisov A.V., Chernov I.A., Avdalyan A.M., Timofeev S.E., Ronzin A.V., Nichiporov A.I., Kukushkin V.I., Kirillov Yu.A. Use of endogenous pigment analytes to assess the invasive potential of superficial skin melanomas. Biomedical Photonics. 2026;15(1):4-10. https://doi.org/10.24931/2413-9432-2026-15-1-4-10
JATS XML


























