Antitumor Therapy under Hypoxic Microenvironment by the Combination of 2-Methoxyestradiol and Sodium Dichloroacetate on Human Non-Small-Cell Lung Cancer

Author:

Romero Yair1ORCID,Castillejos-López Manuel2,Romero-García Susana2,Aguayo Alfonso Salgado2,Herrera Iliana2,Garcia-Martin Misael O.2,Torres-Espíndola Luz Maria3,Negrete-García Maria Cristina2,Olvera Angel Camarena2,Huerta-Cruz Juan Carlos2,Velázquez-Cruz Rafael4ORCID,Cisneros José2,Soto Edgar Flores5,Solís-Chagoyán Héctor6ORCID,Mendoza-Milla Criselda2,Cabello-Gutiérrez Carlos2,Ruiz Víctor2ORCID,Aquino-Gálvez Arnoldo2ORCID

Affiliation:

1. Facultad de Ciencias, Universidad Nacional Autónoma de México, CDMX, Mexico

2. Instituto Nacional de Enfermedades Respiratorias “Ismael Cosío Villegas”, CDMX, Mexico

3. Instituto Nacional de Pediatría, CDMX, Mexico

4. Instituto Nacional de Medicina Genómica, CDMX, Mexico

5. Facultad de Medicina, Universidad Nacional Autónoma México, CDMX, Mexico

6. Instituto Nacional de Psiquiatría “Ramón de la Fuente Muñiz”, CDMX, Mexico

Abstract

A hypoxic microenvironment is a hallmark in different types of tumors; this phenomenon participates in a metabolic alteration that confers resistance to treatments. Because of this, it was proposed that a combination of 2-methoxyestradiol (2-ME) and sodium dichloroacetate (DCA) could reduce this alteration, preventing proliferation through the reactivation of aerobic metabolism in lung adenocarcinoma cell line (A549). A549 cells were cultured in a hypoxic chamber at 1% O2 for 72 hours to determine the effect of this combination on growth, migration, and expression of hypoxia-inducible factors (HIFs) by immunofluorescence. The effect in the metabolism was evaluated by the determination of glucose/glutamine consumption and the lactate/glutamate production. The treatment of 2-ME (10 μM) in combination with DCA (40 mM) under hypoxic conditions showed an inhibitory effect on growth and migration. Notably, this reduction could be attributed to 2-ME, while DCA had a predominant effect on metabolic activity. Moreover, this combination decreases the signaling of HIF-3α and partially HIF-1α but not HIF-2α. The results of this study highlight the antitumor activity of the combination of 2-ME 10 μl/DCA 40 mM, even in hypoxic conditions.

Publisher

Hindawi Limited

Subject

Cell Biology,Ageing,General Medicine,Biochemistry

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