PhD Scientific Days 2024

Molecular Medicine I.

Analysis of the potential role of the GLUT1 transporter in type 2 diabetes

Előadó neve

Kulin, Anna, MSc

Neptun code

HKNL6H

Előadó munkahelye

Research Centre for Natural Sciences

Előadó telefonszáma

+36205335344

Előadó e-mail címe

kulin.anna@gmail.com

Az előadás címe

Analysis of the potential role of the GLUT1 transporter in type 2 diabetes

Szerző(k) neve és munkahelye

Anna Kulin^1,2, Nóra Kucsma², Balázs Bohár³, Botond Literáti-Nagy⁴, László Korányi⁴, Judit Cserepes⁵, Anikó Somogyi⁶, Balázs Sarkadi^1,2, Edit Szabó², György Várady^1,2

1: Doctoral School of Molecular Medicine, Semmelweis University, 1085 Budapest, Hungary
2: Institute of Enzymology, Research Centre for Natural Sciences, 1117 Budapest, Hungary
3: Doctoral School of Biology, Eötvös Loránd University, 1117 Budapest, Hungary
4: Drug Research Center, 8230 Balatonfüred, Hungary
5: CellPharma Kft, 1119 Budapest, Hungary
6: 2nd Department of Internal Medicine, Semmelweis University, 1088 Budapest, Hungary

Bemutatás módja

Szóbeli

Szekció

Molecular Medicine I.

Language of the presentation

English

Preferred session

Molecular Medicine

Összefoglaló szövege

Introduction: Type 2 diabetes mellitus (T2DM) is a complex metabolic disease and various membrane transporters affect its development, progression, or treatments. The GLUT1 membrane protein is a key glucose transporter in numerous cell types and the expression level of this protein has a role in several diseases, including cancer, Alzheimer’s disease and T2DM.
Aims: In this work my aim was to studying the genetic and regulatory background of the expression level of GLUT1 and to analyze its possible association with T2DM.
Methods: The expression level of GLUT1 was measured in red blood cells (RBCs) by flow cytometry, while the genetic background was analyzed by qPCR and luciferase assay.
Result: We found significant associations between RBC GLUT1 levels and four SNPs. In individuals with the minor alleles of rs841848, rs1385129, and rs11537641 had increased, while in those having the variant rs841847 had decreased erythrocyte GLUT1 levels. In the luciferase reporter studies performed in HEK-293T and HepG2 cells, a similar SNP-dependent modulation was observed in most cases. These associations were linked to potential regulatory factors, including reduced glucose or serum levels, hypoxic conditions, and alterations in transcription factor binding sites.
Conclusion: Our research on GLUT1 may contribute to a more detailed understanding of the genetic and regulatory background of GLUT1 expression and its potential role in associated diseases.
Funding:
EFOP-3.6.3-VEKOP-16-2017-00009, Semmelweis University;
NKFIH OTKA (K128011)

University

Semmelweis University

Supervisor

Dr. György Várady

Publication of my abstract

I give consent to the publication of my abstract on the website of the congress.

Kind

Szabad

Status

elfogadva

Accepted presentation method

szóbeli

Előadás fájl jóváhagyás

nem rendelkezett róla

Előadó

5997

Start

10:45

End

10:55