Title of article :
The Main Targets of Okadaic Acid Toxin in Human Intestinal Caco-2 Cells: An Investigation of Biological Systems
Author/Authors :
Robati ، Reza M Skin Research Center - Shahid Beheshti University of Medical Sciences , Razzaghi ، Zahra Laser Application in Medical Sciences Research Center - Shahid Beheshti University of Medical Sciences , Arjmand ، Babak Cell Therapy and Regenerative Medicine Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute - Tehran University of Medical Sciences , Rezaei Tavirani ، Mostafa Proteomics Research Center, Faculty of Paramedical Sciences - Shahid Beheshti University of Medical Sciences , Rostami Nejad ، Mohammad Celiac Disease and Gluten Related Disorders Research Center, Research Institute for Gastroenterology and Liver Disease - Shahid Beheshti University of Medical Sciences , Rezaei ، Mitra Genomic Research Center, Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD) - Shahid Beheshti University of Medical Sciences , Zamanian Azodi ، Mona Proteomics Research Center, Faculty of Paramedical Sciences - Shahid Beheshti University of Medical Sciences
From page :
42997
To page :
42997
Abstract :
Background: Okadaic acid (OA) is a toxin of polluted shellfish. Consuming the contaminated shellfish is accompanied by diarrhea and paralytic and amnesic disorders. There is a correlation between diarrhea and the consumed OA. Determining the critical targeted genes by OA was the aim of this study. Methods: The transcriptomic data about the effect of OA on human intestinal caco-2 cells were extracted from gene expression omnibus (GEO) and evaluated via the GEO2R program. The significant differentially expressed genes (DEGs) were included in a protein-protein interaction (PPI) network and the central nodes were enriched via gene ontology to find the crucial affected biological terms. Results: Among the 178 significant DEGs plus 50 added first neighbors, four hub-bottleneck genes (ALB, FOS, JUN, and MYC) were determined. Twenty-eight critical biological terms were identified as the dysregulated individuals in response to the presence of OA. “ERK1/2-activator protein-1 (AP-1) complex binds KDM6B promoter” was highlighted as the major class of biological terms. Conclusion: It can be concluded that down-regulation of ALB as a potent central gene leads to impairment of blood homeostasis in the presence of OA. Up-regulation of the other three central genes (JUN, FOS, and MYC) grossly affects the vital pathways in the human body.
Keywords :
Okadaic acid , Gene expression , Central gene , Gene ontology , Biological term
Journal title :
International Journal of Medical Toxicology and Forensic Medicine
Journal title :
International Journal of Medical Toxicology and Forensic Medicine
Record number :
2775769
Link To Document :
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