Diphenyl ditelluride anticancer activity and DNA topoisomerase I poisoning in human colon cancer HCT116 cells

• Published in: Oncotarget Vol. 14; no. 1; pp. 637 - 649
• Main Authors: Juchem, André Luiz Mendes, Trindade, Cristiano, da Silva, Juliana Bondan, Machado, Miriana da Silva, Guecheva, Temenouga Nikolova, Rocha, Jaqueline Cesar, Saffi, Jenifer, de Oliveira, Iuri Marques, Henriques, João Antonio Pêgas, Escargueil, Alexandre
• Format: Journal Article
• Language: English
• Published: United States Impact journals 21-06-2023; Impact Journals LLC
• Subjects: Animals; Apoptosis; Colonic Neoplasms - drug therapy; Colonic Neoplasms - metabolism; DNA; DNA Topoisomerases, Type I - metabolism; HCT116 Cells; Humans; Life Sciences; Mammals - metabolism; Research Paper; HCT116; colorectal cancer; diphenyl ditelluride; organotellurium; topoisomerase I; colorectal cancer HCT116 diphenyl ditelluride organotellurium topoisomerase I
• ISSN: 1949-2553; 1949-2553
• DOI: 10.18632/ONCOTARGET.28465

Diphenyl ditelluride (DPDT) is an organotellurium (OT) compound with pharmacological properties, including antioxidant, antigenotoxic and antimutagenic activities when applied at low concentrations. However, DPDT as well as other OT compounds also show cytotoxicity against mammalian cells when treatments occur at higher drug concentrations. Considering that the underlying mechanisms of toxicity of DPDT against tumor cells have been poorly explored, the objective of our study was to investigate the effects of DPDT against both human cancer and non-tumorigenic cells. As a model, we used the colonic HCT116 cancer cells and the MRC5 fibroblasts. Our results showed that DPDT preferentially targets HCT116 cancer cells when compared to MRC5 cells with IC
values of 2.4 and 10.1 μM, respectively. This effect was accompanied by the induction of apoptosis and a pronounced G2/M cell cycle arrest in HCT116 cells. Furthermore, DPDT induces DNA strand breaks at concentrations below 5 μM in HCT116 cells and promotes the occurrence of DNA double strand breaks mostly during S-phase as measured by γ-H2AX/EdU double staining. Finally, DPDT forms covalent complexes with DNA topoisomerase I, as observed by the TARDIS assay, with a more prominent effect observed in HCT116 than in MRC5 cells. Taken together, our results show that DPDT preferentially targets HCT116 colon cancer cells likely through DNA topoisomerase I poisoning. This makes DPDT an interesting molecule for further development as an anti-proliferative compound in the context of cancer.