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Role of thiazolidinediones in adipose tissue remodeling

Undergraduate #104
Discipline: Computer Sciences and Information Management
Subcategory: Computer Science & Information Systems
Session: 2
Room: Exhibit Hall

Victoria Pellot Ortiz - University of Puerto Rico in Aguadilla
Co-Author(s): Mirian De Siqueira, Sicheng Zhang, Claudio VillanuevaInstitute for Quantitative and Computational Biosciences, UCLA



Adipose tissue is a plastic and heterogenous tissue involved in many metabolic processes such as insulin response, food intake, energy storage and thermogenesis. It is also involved in several diseases such as diabetes, cardiovascular disease, and obesity. There are three types of adipocytes: white, beige, and brown; white functions for energy storage while brown and beige, for thermogenesis. PPAR-y is a major transcription factor that is highly expressed in adipocytes. Therefore, we hypothesized that the most relevant pathways will be involved in the PPAR-y pathway and fat oxidation. Activation of PPAR-y by thiazolidinediones has a significant antidiabetic response; however, the detailed mechanism of action is still unclear. RNA-Seq analysis of brown, epidydimal and inguinal adipose tissue was performed on a genetic mouse model of obesity (type 2 diabetes) after treatment with the Pparg agonist, rosiglitazone. We observed a greater number of overlapping genes between brown and inguinal. For the downstream analysis, we focused on the overlapping up-regulated genes from the three tissues because it provides a common rosiglitazone-driven remodeling. We found that within this list of genes the oxidoreductase, carboxylic acid metabolism and Pparg signaling pathways were enriched. Recognizing the pathways with the highest relevance to different processes occurring within the adipose tissue will allow us to understand the mechanisms by which rosiglitazone and other TZDs work as anti-diabetic drugs and help combat obesity.

Funder Acknowledgement(s): UCLA QcB bio BIG summer program

Faculty Advisor: Nancy Cardona Cordero, nancy.cardona@upr.edu

Role: Worked with data collection, analysis and organization of the information from the experiment. Also did the Gene enrichment analysis of the genes present in each pathway.

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This material is based upon work supported by the National Science Foundation (NSF) under Grant No. DUE-1930047. Any opinions, findings, interpretations, conclusions or recommendations expressed in this material are those of its authors and do not represent the views of the AAAS Board of Directors, the Council of AAAS, AAAS’ membership or the National Science Foundation.

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