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Chemical Starting Matter for HNF4α Ligand Discovery and Chemogenomics

Hepatocyte nuclear factor 4α (HNF4α) is a ligand-sensing transcription factor and presents as a potential drug target in metabolic diseases and cancer. In humans, mutations in the HNF4α gene cause maturity-onset diabetes of the young (MODY), and the elevated activity of this protein has been associa...

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Detalles Bibliográficos
Autores principales: Meijer, Isabelle, Willems, Sabine, Ni, Xiaomin, Heering, Jan, Chaikuad, Apirat, Merk, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660650/
https://www.ncbi.nlm.nih.gov/pubmed/33114319
http://dx.doi.org/10.3390/ijms21217895
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author Meijer, Isabelle
Willems, Sabine
Ni, Xiaomin
Heering, Jan
Chaikuad, Apirat
Merk, Daniel
author_facet Meijer, Isabelle
Willems, Sabine
Ni, Xiaomin
Heering, Jan
Chaikuad, Apirat
Merk, Daniel
author_sort Meijer, Isabelle
collection PubMed
description Hepatocyte nuclear factor 4α (HNF4α) is a ligand-sensing transcription factor and presents as a potential drug target in metabolic diseases and cancer. In humans, mutations in the HNF4α gene cause maturity-onset diabetes of the young (MODY), and the elevated activity of this protein has been associated with gastrointestinal cancers. Despite the high therapeutic potential, available ligands and structure–activity relationship knowledge for this nuclear receptor are scarce. Here, we disclose a chemically diverse collection of orthogonally validated fragment-like activators as well as inverse agonists, which modulate HNF4α activity in a low micromolar range. These compounds demonstrate the druggability of HNF4α and thus provide a starting point for medicinal chemistry as well as an early tool for chemogenomics.
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spelling pubmed-76606502020-11-13 Chemical Starting Matter for HNF4α Ligand Discovery and Chemogenomics Meijer, Isabelle Willems, Sabine Ni, Xiaomin Heering, Jan Chaikuad, Apirat Merk, Daniel Int J Mol Sci Communication Hepatocyte nuclear factor 4α (HNF4α) is a ligand-sensing transcription factor and presents as a potential drug target in metabolic diseases and cancer. In humans, mutations in the HNF4α gene cause maturity-onset diabetes of the young (MODY), and the elevated activity of this protein has been associated with gastrointestinal cancers. Despite the high therapeutic potential, available ligands and structure–activity relationship knowledge for this nuclear receptor are scarce. Here, we disclose a chemically diverse collection of orthogonally validated fragment-like activators as well as inverse agonists, which modulate HNF4α activity in a low micromolar range. These compounds demonstrate the druggability of HNF4α and thus provide a starting point for medicinal chemistry as well as an early tool for chemogenomics. MDPI 2020-10-24 /pmc/articles/PMC7660650/ /pubmed/33114319 http://dx.doi.org/10.3390/ijms21217895 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 Communication
Meijer, Isabelle
Willems, Sabine
Ni, Xiaomin
Heering, Jan
Chaikuad, Apirat
Merk, Daniel
Chemical Starting Matter for HNF4α Ligand Discovery and Chemogenomics
title Chemical Starting Matter for HNF4α Ligand Discovery and Chemogenomics
title_full Chemical Starting Matter for HNF4α Ligand Discovery and Chemogenomics
title_fullStr Chemical Starting Matter for HNF4α Ligand Discovery and Chemogenomics
title_full_unstemmed Chemical Starting Matter for HNF4α Ligand Discovery and Chemogenomics
title_short Chemical Starting Matter for HNF4α Ligand Discovery and Chemogenomics
title_sort chemical starting matter for hnf4α ligand discovery and chemogenomics
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7660650/
https://www.ncbi.nlm.nih.gov/pubmed/33114319
http://dx.doi.org/10.3390/ijms21217895
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