Glyphosate and Aminomethylphosphonic Acid (AMPA) Modulate Glutathione S-Transferase in Non-Tumorigenic Prostate Cells

• Published in: International journal of molecular sciences Vol. 24; no. 7; p. 6323
• Main Authors: Borges, Dayanne Silva, Vecchi, Lara, Barros, Deysse Carla Tolentino, Arruda, Vinícius Marques, Ferreira, Helen Soares Valença, da Silva, Matheus Fernandes, Guerra, Joyce Ferreira da Costa, Siqueira, Raoni Pais, Araújo, Thaise Gonçalves
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 28.03.2023; MDPI
• Subjects: Agricultural production; Agriculture; alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid; aminomethylphosphonic acid; Cancer; Cell lines; Cell proliferation; Cell viability; Coffee industry; Cytotoxicity; Enzymes; Gene expression; Glutathione Transferase; Glycine; Glyphosate; Herbicides; Herbicides - metabolism; Herbicides - pharmacology; Humans; Low concentrations; Male; Metabolism; Metabolites; Microorganisms; mRNA; organophosphate; Oxidative stress; Pesticides; Prostate; Prostate - metabolism; Proteins; Scientific equipment and supplies industry; Tetrazoles - pharmacology; Thiols; Brazil; United States; Massachusetts; organophosphate; metabolism; prostate; transcripts; aminomethylphosphonic acid; glyphosate
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms24076323

Glyphosate (GLY) was developed in the early 1970s and has become the most used broad-spectrum herbicide in the world so far. Its main metabolite is aminomethylphosphonic acid (AMPA), and the accumulation of GLY and its derivative compounds raises some concerns regarding possible health outcomes. In this study, we aimed to evaluate the effects of GLY and AMPA on prostate cell lines by evaluating cell viability, proliferation, gene and protein expression, and cellular pathways involved in the response to oxidative stress. Our results indicated that GLY and AMPA reduced the cell viability of tumorigenic and non-tumorigenic prostate cell lines only at higher concentrations (10 mM GLY and 20 mM AMPA). In contrast, both compounds increased the clonogenicity of non-tumorigenic PNT2 cells, mainly at concentrations below the IC (5 mM GLY and 10 mM AMPA). Moreover, treatment of non-tumorigenic cells with low concentrations of GLY or AMPA for 48 h increased GSTM3 expression at both mRNA and protein levels. In contrast, the treatments decrease the GST activity and induced an increase in oxidative stress, mainly at lower concentrations. Therefore, both compounds can cause cellular damage even at lower concentrations in non-tumorigenic PNT2 cells, mainly affecting cell proliferation and oxidative stress.