Adriana Miguel-Alvarez

Dr. Adriana Miguel-Alvarez

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Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 September 2023 in Clinical Rheumatology
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MMManuel Martínez-Lavín
Manuel Martínez-Lavín
AMAdriana Miguel-Alvarez
Adriana Miguel-Alvarez

10 January 2022 in Revista de la Facultad de Medicina
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Journal Article
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AMAdriana Miguel-Alvarez
Adriana Miguel-Alvarez
Revista de la Facultad de Medicina de la UNAM

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Journal Article
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LALuis M Amezcua-Guerra
Luis M Amezcua-Guerra
MSMaría G. Soberanes-García
María G. Soberanes-García
LBLaura Barragán-Huerta
Laura Barragán-Huerta
YJYaneli Juárez-Vicuña
Yaneli Juárez-Vicuña
AMAdriana Miguel-Alvarez
Adriana Miguel-Alvarez
MBMalinalli Brianza-Padilla
Malinalli Brianza-Padilla
This study aimed to evaluate whether serum from patients with primary antiphospholipid syndrome (APS) is associated with changes in the expression of long non-coding RNAs (lncRNAs) in endothelial cells. Human umbilical vein endothelial cells (HUVECs) were cultured with serum from 12 female patients with APS or 8 age-matched healthy female controls. The expression levels of HIF1A-AS1, OIP5-AS1, and GAS5 were quantified by RT-qPCR. Exposure of HUVECs to APS serum was associated with reduced expression of HIF1A-AS1 and OIP5-AS1 compared with cells stimulated with control serum. The median HIF1A-AS1 expression levels were 0.08 a.u. (interquartile range, 0.06–0.10) in APS-stimulated cells versus 0.14 a.u. (0.08–0.16) in controls (p = 0.044). Likewise, OIP5-AS1 levels were 0.09 a.u. (0.01–0.16) in APS-stimulated cells versus 2.24 a.u. (0.70–3.55) in controls (p = 0.018). In contrast, GAS5 expression did not differ significantly between groups (340 a.u. (310–3940 versus 358 a.u. (163–445); p = 0.290). In this proof-of-concept study, serum from APS patients was associated with selective downregulation of HIF1A-AS1 and OIP5-AS1 in endothelial cells. These findings support a potential link between circulating APS-related factors and endothelial lncRNA expression; however, no mechanistic or functional conclusions can be drawn.