Cargando…
Grainyhead-like (Grhl) Target Genes in Development and Cancer
Grainyhead-like (GRHL) factors are essential, highly conserved transcription factors (TFs) that regulate processes common to both natural cellular behaviours during embryogenesis, and de-regulation of growth and survival pathways in cancer. Serving to drive the transcription, and therefore activatio...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911041/ https://www.ncbi.nlm.nih.gov/pubmed/35269877 http://dx.doi.org/10.3390/ijms23052735 |
_version_ | 1784666676787150848 |
---|---|
author | Gasperoni, Jemma G. Fuller, Jarrad N. Darido, Charbel Wilanowski, Tomasz Dworkin, Sebastian |
author_facet | Gasperoni, Jemma G. Fuller, Jarrad N. Darido, Charbel Wilanowski, Tomasz Dworkin, Sebastian |
author_sort | Gasperoni, Jemma G. |
collection | PubMed |
description | Grainyhead-like (GRHL) factors are essential, highly conserved transcription factors (TFs) that regulate processes common to both natural cellular behaviours during embryogenesis, and de-regulation of growth and survival pathways in cancer. Serving to drive the transcription, and therefore activation of multiple co-ordinating pathways, the three GRHL family members (GRHL1-3) are a critical conduit for modulating the molecular landscape that guides cellular decision-making processes during proliferation, epithelial-mesenchymal transition (EMT) and migration. Animal models and in vitro approaches harbouring GRHL loss or gain-of-function are key research tools to understanding gene function, which gives confidence that resultant phenotypes and cellular behaviours may be translatable to humans. Critically, identifying and characterising the target genes to which these factors bind is also essential, as they allow us to discover and understand novel genetic pathways that could ultimately be used as targets for disease diagnosis, drug discovery and therapeutic strategies. GRHL1-3 and their transcriptional targets have been shown to drive comparable cellular processes in Drosophila, C. elegans, zebrafish and mice, and have recently also been implicated in the aetiology and/or progression of a number of human congenital disorders and cancers of epithelial origin. In this review, we will summarise the state of knowledge pertaining to the role of the GRHL family target genes in both development and cancer, primarily through understanding the genetic pathways transcriptionally regulated by these factors across disparate disease contexts. |
format | Online Article Text |
id | pubmed-8911041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89110412022-03-11 Grainyhead-like (Grhl) Target Genes in Development and Cancer Gasperoni, Jemma G. Fuller, Jarrad N. Darido, Charbel Wilanowski, Tomasz Dworkin, Sebastian Int J Mol Sci Review Grainyhead-like (GRHL) factors are essential, highly conserved transcription factors (TFs) that regulate processes common to both natural cellular behaviours during embryogenesis, and de-regulation of growth and survival pathways in cancer. Serving to drive the transcription, and therefore activation of multiple co-ordinating pathways, the three GRHL family members (GRHL1-3) are a critical conduit for modulating the molecular landscape that guides cellular decision-making processes during proliferation, epithelial-mesenchymal transition (EMT) and migration. Animal models and in vitro approaches harbouring GRHL loss or gain-of-function are key research tools to understanding gene function, which gives confidence that resultant phenotypes and cellular behaviours may be translatable to humans. Critically, identifying and characterising the target genes to which these factors bind is also essential, as they allow us to discover and understand novel genetic pathways that could ultimately be used as targets for disease diagnosis, drug discovery and therapeutic strategies. GRHL1-3 and their transcriptional targets have been shown to drive comparable cellular processes in Drosophila, C. elegans, zebrafish and mice, and have recently also been implicated in the aetiology and/or progression of a number of human congenital disorders and cancers of epithelial origin. In this review, we will summarise the state of knowledge pertaining to the role of the GRHL family target genes in both development and cancer, primarily through understanding the genetic pathways transcriptionally regulated by these factors across disparate disease contexts. MDPI 2022-03-01 /pmc/articles/PMC8911041/ /pubmed/35269877 http://dx.doi.org/10.3390/ijms23052735 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Gasperoni, Jemma G. Fuller, Jarrad N. Darido, Charbel Wilanowski, Tomasz Dworkin, Sebastian Grainyhead-like (Grhl) Target Genes in Development and Cancer |
title | Grainyhead-like (Grhl) Target Genes in Development and Cancer |
title_full | Grainyhead-like (Grhl) Target Genes in Development and Cancer |
title_fullStr | Grainyhead-like (Grhl) Target Genes in Development and Cancer |
title_full_unstemmed | Grainyhead-like (Grhl) Target Genes in Development and Cancer |
title_short | Grainyhead-like (Grhl) Target Genes in Development and Cancer |
title_sort | grainyhead-like (grhl) target genes in development and cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911041/ https://www.ncbi.nlm.nih.gov/pubmed/35269877 http://dx.doi.org/10.3390/ijms23052735 |
work_keys_str_mv | AT gasperonijemmag grainyheadlikegrhltargetgenesindevelopmentandcancer AT fullerjarradn grainyheadlikegrhltargetgenesindevelopmentandcancer AT daridocharbel grainyheadlikegrhltargetgenesindevelopmentandcancer AT wilanowskitomasz grainyheadlikegrhltargetgenesindevelopmentandcancer AT dworkinsebastian grainyheadlikegrhltargetgenesindevelopmentandcancer |