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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7660650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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