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Transcript Levels of Aldo-Keto Reductase Family 1 Subfamily C (AKR1C) Are Increased in Prostate Tissue of Patients with Type 2 Diabetes

Aldo-keto reductase family 1 (AKR1) enzymes play a crucial role in diabetic complications. Since type 2 diabetes (T2D) is associated with cancer progression, we investigated the impact of diabetes on AKR1 gene expression in the context of prostate cancer (PCa) development. In this study, we analyzed...

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Autores principales: Franko, Andras, Berti, Lucia, Hennenlotter, Jörg, Rausch, Steffen, Scharpf, Marcus O., de Angelis, Martin Hrabĕ, Stenzl, Arnulf, Birkenfeld, Andreas L., Peter, Andreas, Lutz, Stefan Z., Häring, Hans-Ulrich, Heni, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564141/
https://www.ncbi.nlm.nih.gov/pubmed/32932589
http://dx.doi.org/10.3390/jpm10030124
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author Franko, Andras
Berti, Lucia
Hennenlotter, Jörg
Rausch, Steffen
Scharpf, Marcus O.
de Angelis, Martin Hrabĕ
Stenzl, Arnulf
Birkenfeld, Andreas L.
Peter, Andreas
Lutz, Stefan Z.
Häring, Hans-Ulrich
Heni, Martin
author_facet Franko, Andras
Berti, Lucia
Hennenlotter, Jörg
Rausch, Steffen
Scharpf, Marcus O.
de Angelis, Martin Hrabĕ
Stenzl, Arnulf
Birkenfeld, Andreas L.
Peter, Andreas
Lutz, Stefan Z.
Häring, Hans-Ulrich
Heni, Martin
author_sort Franko, Andras
collection PubMed
description Aldo-keto reductase family 1 (AKR1) enzymes play a crucial role in diabetic complications. Since type 2 diabetes (T2D) is associated with cancer progression, we investigated the impact of diabetes on AKR1 gene expression in the context of prostate cancer (PCa) development. In this study, we analyzed benign (BEN) prostate and PCa tissue of patients with and without T2D. Furthermore, to replicate hyperglycemia in vitro, we treated the prostate adenocarcinoma cell line PC3 with increasing glucose concentrations. Gene expression was quantified using real-time qPCR. In the prostate tissue of patients with T2D, AKR1C1 and AKR1C2 transcripts were higher compared to samples of patients without diabetes. In PC3 cells, high glucose treatment induced the gene expression levels of AKR1C1, C2, and C3. Furthermore, both in human tissue and in PC3 cells, the transcript levels of AKR1C1, C2, and C3 showed positive associations with oncogenes, which are involved in proliferation processes and HIF1α and NFκB pathways. These results indicate that in the prostate glands of patients with T2D, hyperglycemia could play a pivotal role by inducing the expression of AKR1C1, C2, and C3. The higher transcript level of AKR1C was furthermore associated with upregulated HIF1α and NFκB pathways, which are major drivers of PCa carcinogenesis.
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spelling pubmed-75641412020-10-26 Transcript Levels of Aldo-Keto Reductase Family 1 Subfamily C (AKR1C) Are Increased in Prostate Tissue of Patients with Type 2 Diabetes Franko, Andras Berti, Lucia Hennenlotter, Jörg Rausch, Steffen Scharpf, Marcus O. de Angelis, Martin Hrabĕ Stenzl, Arnulf Birkenfeld, Andreas L. Peter, Andreas Lutz, Stefan Z. Häring, Hans-Ulrich Heni, Martin J Pers Med Article Aldo-keto reductase family 1 (AKR1) enzymes play a crucial role in diabetic complications. Since type 2 diabetes (T2D) is associated with cancer progression, we investigated the impact of diabetes on AKR1 gene expression in the context of prostate cancer (PCa) development. In this study, we analyzed benign (BEN) prostate and PCa tissue of patients with and without T2D. Furthermore, to replicate hyperglycemia in vitro, we treated the prostate adenocarcinoma cell line PC3 with increasing glucose concentrations. Gene expression was quantified using real-time qPCR. In the prostate tissue of patients with T2D, AKR1C1 and AKR1C2 transcripts were higher compared to samples of patients without diabetes. In PC3 cells, high glucose treatment induced the gene expression levels of AKR1C1, C2, and C3. Furthermore, both in human tissue and in PC3 cells, the transcript levels of AKR1C1, C2, and C3 showed positive associations with oncogenes, which are involved in proliferation processes and HIF1α and NFκB pathways. These results indicate that in the prostate glands of patients with T2D, hyperglycemia could play a pivotal role by inducing the expression of AKR1C1, C2, and C3. The higher transcript level of AKR1C was furthermore associated with upregulated HIF1α and NFκB pathways, which are major drivers of PCa carcinogenesis. MDPI 2020-09-12 /pmc/articles/PMC7564141/ /pubmed/32932589 http://dx.doi.org/10.3390/jpm10030124 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Franko, Andras
Berti, Lucia
Hennenlotter, Jörg
Rausch, Steffen
Scharpf, Marcus O.
de Angelis, Martin Hrabĕ
Stenzl, Arnulf
Birkenfeld, Andreas L.
Peter, Andreas
Lutz, Stefan Z.
Häring, Hans-Ulrich
Heni, Martin
Transcript Levels of Aldo-Keto Reductase Family 1 Subfamily C (AKR1C) Are Increased in Prostate Tissue of Patients with Type 2 Diabetes
title Transcript Levels of Aldo-Keto Reductase Family 1 Subfamily C (AKR1C) Are Increased in Prostate Tissue of Patients with Type 2 Diabetes
title_full Transcript Levels of Aldo-Keto Reductase Family 1 Subfamily C (AKR1C) Are Increased in Prostate Tissue of Patients with Type 2 Diabetes
title_fullStr Transcript Levels of Aldo-Keto Reductase Family 1 Subfamily C (AKR1C) Are Increased in Prostate Tissue of Patients with Type 2 Diabetes
title_full_unstemmed Transcript Levels of Aldo-Keto Reductase Family 1 Subfamily C (AKR1C) Are Increased in Prostate Tissue of Patients with Type 2 Diabetes
title_short Transcript Levels of Aldo-Keto Reductase Family 1 Subfamily C (AKR1C) Are Increased in Prostate Tissue of Patients with Type 2 Diabetes
title_sort transcript levels of aldo-keto reductase family 1 subfamily c (akr1c) are increased in prostate tissue of patients with type 2 diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564141/
https://www.ncbi.nlm.nih.gov/pubmed/32932589
http://dx.doi.org/10.3390/jpm10030124
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