Toxins of okadaic acid-group increase malignant properties in cells of colon cancer
Author
dc.contributor.author
Jiménez Cárcamo, Danae
Author
dc.contributor.author
García Carrasco, Carlos
Author
dc.contributor.author
Contreras Muñoz, Héctor
Admission date
dc.date.accessioned
2020-05-15T16:12:08Z
Available date
dc.date.available
2020-05-15T16:12:08Z
Publication date
dc.date.issued
2020
Cita de ítem
dc.identifier.citation
Toxins (2020) 12: 179
es_ES
Identifier
dc.identifier.other
10.3390/toxins12030179
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/174759
Abstract
dc.description.abstract
iarrhetic shellfish poisoning (DSP) is a syndrome caused by the intake of shellfish contaminated with a group of lipophilic and thermostable toxins, which consists of okadaic acid (OA), dinophysistoxin-1 (DTX-1) and dinophysistoxin-2 (DTX-2). These toxins are potent protein Ser/Thr phosphatase inhibitors, mainly type 1 protein phosphatase (PP1) and type 2A protein phosphatase (PP2A). Different effects have been reported at the cellular, molecular and genetic levels. In this study, changes in cell survival and cell mobility induced by OA, DTX-1 and DTX-2 were determined in epithelial cell lines of the colon and colon cancer. The cell viability results showed that tumoral cell lines were more resistant to toxins than the nontumoral cell line. The results of the functional assays for testing cell migration, evaluation of cell death and the expression of proteins associated with cell adhesion showed a dual effect of toxins since in the nontumoral cell line, a greater induction of cell death, presumably by anoikis, was detected. In the tumoral cell lines, there was an induction of a more aggressive phenotype characterized by increased resistance to toxins, increased migration and increased FAK activation. In tumoral cell lines of colon cancer, OA, DTX-1/DTX-2 induce a more aggressive phenotype.
es_ES
Patrocinador
dc.description.sponsorship
Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)
CONICYT FONDECYT
1151214
1160168
Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)
22160169