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

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 alt...

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Veröffentlicht in:Oxidative medicine and cellular longevity 2020, Vol.2020 (2020), p.1-12
Hauptverfasser: Olvera, Angel Camarena, Huerta-Cruz, Juan Carlos, Velázquez-Cruz, Rafael, Soto, Edgar Flores, Solís-Chagoyán, Héctor, Mendoza-Milla, Criselda, Cabello-Gutiérrez, Carlos, Ruiz, Víctor, Aquino-Gálvez, Arnoldo, Negrete-García, Maria Cristina, Torres-Espíndola, Luz Maria, Garcia-Martin, Misael O., Herrera, Iliana, Aguayo, Alfonso Salgado, Romero-García, Susana, Castillejos-López, Manuel, Romero, Yair, Cisneros, José
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Sprache:eng
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Zusammenfassung: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.
ISSN:1942-0900
1942-0994
DOI:10.1155/2020/3176375