Author(s): Amaral, Leslie Ann Silva ; Mendes, Filipa ; Côrte-Real, Manuela ; Sousa, Maria João ; Chaves, Susana Alexandra Rodrigues
Date: 2020
Persistent ID: http://hdl.handle.net/1822/72948
Origin: RepositóriUM - Universidade do Minho
Subject(s): Ciências Naturais::Ciências Biológicas; Engenharia e Tecnologia::Biotecnologia Ambiental; Science & Technology
Cisplatin is a widely used antineoplastic agent that has DNA as the main target, though cellular resistance hampers its therapeutic efficacy. An emerging hallmark of cancer cells is their altered metabolism, characterized by increased glycolysis even under aerobic conditions, with increased lactate production (known as the Warburg effect). Although this altered metabolism often results in increased resistance to chemotherapy, it also provides an opportunity for targeted therapeutic intervention. It has been suggested that cisplatin cytotoxicity can be affected by tumor metabolism, though with varying effects. We therefore sought to better characterize how lactate affects cisplatin sensitivity in the simplified Saccharomyces cerevisiae model. We show that lactate renders yeast cells resistant to cisplatin, independently of growth rate or respiration ability. We further show that histone acetylation is not affected, but histone phosphorylation is decreased in lactate-containing media. Finally, we show that Rad4p, essential for nucleotide excision repair, is required for the observed phenotype and thus likely underlies the mechanism responsible for lactate-mediated resistance to cisplatin. Overall, understanding how lactate modulates cisplatin sensitivity will aid in the development of new strategies to overcome drug resistance.
This work was supported by the "Contrato-Programa" (UID/BIA/04050/2020) funded by national funds through FCT I.P., as well as a Post-doc fellowship to S. Chaves (SFRH/BPD/89980/2012).
