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Photodynamic therapy combined to cisplatin potentiates cell death responses of cervical cancer cells.
de Freitas, Laura Marise; Serafim, Rodolfo Bortolozo; de Sousa, Juliana Ferreira; Moreira, Thaís Fernanda; Dos Santos, Cláudia Tavares; Baviera, Amanda Martins; Valente, Valeria; Soares, Christiane Pienna; Fontana, Carla Raquel.
Afiliación
  • de Freitas LM; Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara- Rod Araraquara-Jau km 01 s/n, Araraquara, Sao Paulo, 14800-903, Brazil.
  • Serafim RB; Faculdade de Medicina de Ribeirao Preto, USP Univ de Sao Paulo, Avenida dos Bandeirantes 3900, Ribeirao Preto, Sao Paulo, 14049-900, Brazil.
  • de Sousa JF; Faculdade de Medicina de Ribeirao Preto, USP Univ de Sao Paulo, Avenida dos Bandeirantes 3900, Ribeirao Preto, Sao Paulo, 14049-900, Brazil.
  • Moreira TF; Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara- Rod Araraquara-Jau km 01 s/n, Araraquara, Sao Paulo, 14800-903, Brazil.
  • Dos Santos CT; Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara- Rod Araraquara-Jau km 01 s/n, Araraquara, Sao Paulo, 14800-903, Brazil.
  • Baviera AM; Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara- Rod Araraquara-Jau km 01 s/n, Araraquara, Sao Paulo, 14800-903, Brazil.
  • Valente V; Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara- Rod Araraquara-Jau km 01 s/n, Araraquara, Sao Paulo, 14800-903, Brazil.
  • Soares CP; Faculdade de Medicina de Ribeirao Preto, USP Univ de Sao Paulo, Avenida dos Bandeirantes 3900, Ribeirao Preto, Sao Paulo, 14049-900, Brazil.
  • Fontana CR; Universidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquara- Rod Araraquara-Jau km 01 s/n, Araraquara, Sao Paulo, 14800-903, Brazil.
BMC Cancer ; 17(1): 123, 2017 02 10.
Article en En | MEDLINE | ID: mdl-28187758
ABSTRACT

BACKGROUND:

Photodynamic therapy (PDT) has proven to be a promising alternative to current cancer treatments, especially if combined with conventional approaches. The technique is based on the administration of a non-toxic photosensitizing agent to the patient with subsequent localized exposure to a light source of a specific wavelength, resulting in a cytotoxic response to oxidative damage. The present study intended to evaluate in vitro the type of induced death and the genotoxic and mutagenic effects of PDT alone and associated with cisplatin.

METHODS:

We used the cell lines SiHa (ATCC® HTB35™), C-33 A (ATCC® HTB31™) and HaCaT cells, all available at Dr. Christiane Soares' Lab. Photosensitizers were Photogem (PGPDT) and methylene blue (MBPDT), alone or combined with cisplatin. Cell death was accessed through Hoechst and Propidium iodide staining and caspase-3 activity. Genotoxicity and mutagenicity were accessed via flow cytometry with anti-gama-H2AX and micronuclei assay, respectively. Data were analyzed by one-way ANOVA with Tukey's posthoc test.

RESULTS:

Both MBPDT and PGPDT induced caspase-independent death, but MBPDT induced the morphology of typical necrosis, while PGPDT induced morphological alterations most similar to apoptosis. Cisplatin predominantly induced apoptosis, and the combined therapy induced variable rates of apoptosis- or necrosis-like phenotypes according to the cell line, but the percentage of dead cells was always higher than with monotherapies. MBPDT, either as monotherapy or in combination with cisplatin, was the unique therapy to induce significant damage to DNA (double strand breaks) in the three cell lines evaluated. However, there was no mutagenic potential observed for the damage induced by MBPDT, since the few cells that survived the treatment have lost their clonogenic capacity.

CONCLUSIONS:

Our results elicit the potential of combined therapy in diminishing the toxicity of antineoplastic drugs. Ultimately, photodynamic therapy mediated by either methylene blue or Photogem as monotherapy or in combination with cisplatin has low mutagenic potential, which supports its safe use in clinical practice for the treatment of cervical cancer.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Cisplatino / Apoptosis / Luz Límite: Female / Humans Idioma: En Revista: BMC Cancer Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Asunto principal: Cisplatino / Apoptosis / Luz Límite: Female / Humans Idioma: En Revista: BMC Cancer Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article País de afiliación: Brasil