Gene Expression Profile of Placenta and Adipose Tissue in Women with Gestational Diabetes Mellitus
Renata Saucedo, Erika Magallón-Gayón, Rocio Alejandra Chavez-Santoscoy, Mary Flor Díaz-Velázquez, Aldo Ferreira-Hermosillo, Diana Ojeda-López, Wendy Porras-Marcial, Debbie López-Sánchez, Jorge Valencia-Ortega

TL;DR
This study identifies gene expression changes in placenta and fat tissue from women with gestational diabetes, revealing altered molecular pathways linked to the condition.
Contribution
The study provides novel insights into the transcriptomic profiles of placenta and adipose tissue in gestational diabetes mellitus.
Findings
179 differentially expressed genes were identified in placenta, and 4 in visceral adipose tissue of GDM women.
Upregulated placental genes in GDM are enriched in G-protein-coupled receptor signaling and phospholipid metabolism.
Downregulated placental genes in GDM are linked to cell motility and migration, while VAT DEGs relate to cancer and complement activation.
Abstract
Placenta and visceral adipose tissue (VAT) are implicated in the development of gestational diabetes mellitus (GDM). In the present study, we examined the whole-transcriptomic profile of both tissues in GDM women to elucidate the molecular basis of GDM pathogenesis. The whole-transcriptome profile was analyzed in placenta and VAT from at-term patients with GDM and controls using RNA-seq. qPCR was used to validate several differentially expressed genes (DEGs). A total of 179 DEGs were observed in the placenta and 4 in VAT, including both up- and downregulated genes. The expression of the selected mRNAs for validation was consistent with the sequencing results. An analysis of the placental upregulated DEGs in the GDM women showed enrichment in functions including the G-protein-coupled receptor signaling pathway, organophosphate biosynthetic process, and phospholipid metabolic process,…
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Taxonomy
TopicsGestational Diabetes Research and Management · Pregnancy and preeclampsia studies · Cancer-related molecular mechanisms research
