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THE STUDY OF MECHANISMS OF PHOTOINDUCED APOPTOSIS IN THE SKIN MALIGNANT MELANOMA CELL MODEL

https://doi.org/10.24931/2413-9432-2016-5-3-4-8

Abstract

The results of the experimental study of immune response of human skin malignant melanoma cells Mel 226 on photodynamic exposure are represented in the article. Photoinduced apoptosis of skin malignant melanoma was studied in vitro. The study showed that irradiation with the agent fotoditazin at dose of 0.5–2.5 µg/ml (6 and 10 min exposure 30 min before irradiation; irradiation parameters: wavelength of 662 nm, total light dose from 40 to 60 J/cm2) induced early apoptosis. The increase of the time of laser irradiation significantly accelerates the conversion of photosensitized tumor cells from early to late apoptosis.

About the Authors

M. L. Gelfond
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia North-Western State Medical University named after I.I. Mechnikov, Saint-Petersburg, Russia
Russian Federation


I. A. Baldueva
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia North-Western State Medical University named after I.I. Mechnikov, Saint-Petersburg, Russia
Russian Federation


A. S. Barchuk
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia North-Western State Medical University named after I.I. Mechnikov, Saint-Petersburg, Russia
Russian Federation


G. I. Gafton
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia Federal State Budgetary Educational Institution of Higher Education Academician I.P. Pavlov First St. Petersburg State Medical University of the Ministry of Healthcare of Russian Federation, Saint-Petersburg, Russia
Russian Federation


V. V. Anisimov
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia
Russian Federation


Yu. V. Semiletova
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia North-Western State Medical University named after I.I. Mechnikov, Saint-Petersburg, Russia
Russian Federation


A. V. Novik
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia
Russian Federation


M. Yu. Myasnyankin
North-Western State Medical University named after I.I. Mechnikov, Saint-Petersburg, Russia
Russian Federation


T. L. Nekhaeva
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia
Russian Federation


A. B. Danilova
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia
Russian Federation


E. V. Vorobeychikov
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia
Russian Federation


A. I. Vaalj
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia
Russian Federation


I. G. Gafton
Federal State Institution N.N.Petrov Research Institute of Oncology of Federal Agency of High Technology Medical Assistance, Saint-Petersburg, Russia
Russian Federation


References

1. Zlokachestvennye novoobrazovaniya v Rossii v 2009 godu (zabolevae-most' i smertnost') / (Malignant neoplasms in Russia in 2009 (incidence and mortality), by eds. V.I. Chissov, V.V. Starinskii, G.V. Petrova. Mos-cow, OOO Antif Publ., 2011. 260 p.

2. Filonenko E.V., Serova L.G., Urlova A.N. Photodynamic therapy in patients with skin metastases of melanoma, Biomedical Photonics, 2015, Vol. 4, No. 2, pp. 22-25. (in Russian).

3. Merabishvilli V.M. Vyzhivaemost' onkologicheskikh bol'nykh (Survival rate of cancer patients). Saint Petersburg, OOO Firma Kosta Publ., 2006. 438 p.

4. Baldueva I.A. Immune characteristics of tumor–host interaction in melanoma, Prakticheskaya onkologiya, 2001, No. 4(8), pp. 37-41. (in Russian).

5. Gollnick S., Evans S., Baumann H. Role of cytokines in photodynamic therapy-induced local and systemic inflammation, Br. J. Cancer, 2003, Vol. 88, pp. 1772-9.

6. Gollnick S., Vaughan L., Henderson B. Generation of effective antitumor vaccines using photodynamic therapy, Cancer Res., 2002, Vol. 62, pp. 1604-8.

7. Gollnick S.O., Brackett C.M. Enhancement of anti-tumor immunity by photodynamic therapy, Immunol Res., 2010, Vol. 46(1-3), pp. 216-26.

8. Preise D., Oren R, Glinert I., Kalchenko V., Jung S., Scherz A., Salomon Y. Systemic antitumor protection by vascular-targeted photodynamic therapy involves cellular and humoral immunity, Cancer. Immunol. Immunother., 2009, Vol. 58, pp. 71-84.

9. Preise D., Scherz A., Salomon Y. Antitumor immunity promoted by vascular occluding therapy: lessons from vascular-targeted photodynamic therapy (VTP), Photochem Photobiol Sci, 2011, Vol. 10(5), pp. 681-8.

10. Huang Z., Xu H., Meyers A.D., Musani A.I., Wang L., Tagg R., Barqawi A.B., Chen Y.K. Photodynamic therapy for treatment of solid tumors-potential and technical challenges, Technol Cancer Res Treat, 2008, Vol. 7(4), pp. 309-20.

11. Mroz P., Szokalska A., Wu M.X., Hamblin M.R. Photodynamic Therapy of Tumors Can Lead to Development of Systemic Antigen-Specific Immune Response, PLoS ONE, 2010, Vol. 5(12), pp. 151-94.

12. Abels C. Targeting of the vascular system of solid tumours by photodynamic therapy (PDT), Photochem Photobiol Sci, 2004, No. 3, pp. 765-71.

13. Golab J., Wilczynski G., Zagozdzon R., Stoklosa T., Dabrowska A., Rybczynska J., Wasik M., Machaj E., Olda T., Kozar K., Kaminski R., Giermasz A., Czajka A., Lasek W., Feleszko W., Jakobisiak M. Potentiation of the anti-tumor effects of Photofrin-based photodynamic therapy by localized treatment with G-CSF, Br. J. Cancer., 2000, Vol. 82(8), pp. 1485-91.

14. Van Duijnhoven F.H. The immunological consequences of photodynamic treatment of cancer, a literature review, Immunobiology, 2003, Vol. 207, pp. 105-13.

15. Akopov A.L., Kazakov N.V., Rusanov A.A., Karlson A. The mechanisms of photodynamic action for treating of cancer patients, Biomedical Photonics, 2015, Vol. 4, No. 2, pp. 9-16. (in Russian).

16. Almeida R.D., Manadas B.J., Carvalho A.P., Duarte C.B. Intracellular signaling mechanisms in photodynamic therapy, Biochim. Biophys. Acta., 2004, Vol. 1704, pp. 59-86.

17. Kiesslich T., Plaetzer K., Oberdanner C.B., Berlanda J., Obermair F.J., Krammer B. Differential effects of glucose deprivation on the cellular sensitivity towards photodynamic treatment-based production of reactive oxygen species and apoptosis-induction, FEBS Le, 2005, Vol. 579, pp. 185-190.

18. Oberdanner C.B., Kiesslich T., Krammer B., Plaetzer K. Glucose is required to maintain high ATP-levels for the energy-utilizing steps during PDT-induced apoptosis, Photochem Photobiol., 2002, Vol. 76, pp. 695-703.

19. Filonenko E.V. Fluorescence diagnostics and photodynamic therapy: justification of applications and opportunities in oncology, Biomedical Photonics, 2014, Vol. 3, No. 1, pp. 3-7. (in Russian).

20. Wyld L., Reed M.W., Brown N.J. Differential cell death response to photodynamic therapy is dependent on dose and cell type, Br. J. Cancer., 2001, Vol. 84, pp. 1384-86

21. Reed M., Miller F., Weiman T., Tseng M.T., Pietsch C.G. The effect of photodynamic therapy on the microcirculation, J. Surg. Res., 1988, Vol. 45, pp. 452-9.

22. Oleinick N., Morris R., Belichenko I. The role of apoptosis in response to photodynamic therapy: What, where, why and how, Photochem. Photobiol. Sci., 2002, Vol. 1, pp. 1-7.

23. Hayle A.K., Ward T.H., Moore J.V. DNA damage and repair in Gorlin syndrome and normal fibroblasts aer aminolevulinic acid photodynamic therapy: a comet assay study, Photochem. Photobiol., 2003, Vol. 78, pp. 337-41.

24. McNair F.I., Marples B., West C.M., Moore J.V. A comet assay of DNA damage and repair in K562 cells aer photodynamic therapy using haematoporphyrin derivative, methylene blue and meso-tetrahydroxyphenylchlorin, Br J Cancer, 1997, Vol. 75, pp. 1721-9.

25. Woods J.A., Traynor N.J., Brancaleon L., Moseley H. The effect of photo-frin on DNA strand breaks and base oxidation in HaCaT keratinocytes: a comet assay study, Photochem. Photobiol., 2004, Vol. 79, pp. 105-13.


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For citations:


Gelfond M.L., Baldueva I.A., Barchuk A.S., Gafton G.I., Anisimov V.V., Semiletova Yu.V., Novik A.V., Myasnyankin M.Yu., Nekhaeva T.L., Danilova A.B., Vorobeychikov E.V., Vaalj A.I., Gafton I.G. THE STUDY OF MECHANISMS OF PHOTOINDUCED APOPTOSIS IN THE SKIN MALIGNANT MELANOMA CELL MODEL. Biomedical Photonics. 2016;5(3):4-8. (In Russ.) https://doi.org/10.24931/2413-9432-2016-5-3-4-8

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