Evaluating the Expression of Candidate Homeobox Genes and Their Role in Local-Site Inflammation in Mucosal Tissue Obtained from Children with Non-Syndromic Cleft Lip and Palate

Craniofacial development including palatogenesis is a complex process which requires an orchestrated and spatiotemporal expression of various genes and factors for proper embryogenesis and organogenesis. One such group of genes essential for craniofacial development is the homeobox genes, transcript...

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Autores principales: Nityanand Jain, Mara Pilmane
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Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/ce0042b92db24c409f95a16e5af6e644
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spelling oai:doaj.org-article:ce0042b92db24c409f95a16e5af6e6442021-11-25T18:07:28ZEvaluating the Expression of Candidate Homeobox Genes and Their Role in Local-Site Inflammation in Mucosal Tissue Obtained from Children with Non-Syndromic Cleft Lip and Palate10.3390/jpm111111352075-4426https://doaj.org/article/ce0042b92db24c409f95a16e5af6e6442021-11-01T00:00:00Zhttps://www.mdpi.com/2075-4426/11/11/1135https://doaj.org/toc/2075-4426Craniofacial development including palatogenesis is a complex process which requires an orchestrated and spatiotemporal expression of various genes and factors for proper embryogenesis and organogenesis. One such group of genes essential for craniofacial development is the homeobox genes, transcriptional factors that are commonly associated with congenital abnormalities. Amongst these genes, <i>DLX4, HOXB3,</i> and <i>MSX2</i> have been recently shown to be involved in the etiology of non-syndromic cleft lip and palate. Hence, we investigated the gene and protein expression of these genes in normal and cleft affected mucosal tissue obtained from 22 children, along with analyzing their role in promoting local-site inflammation using <i>NF-κB</i>. Additionally, we investigated the role of <i>PTX3,</i> which plays a critical role in tissue remodeling and wound repair. We found a residual gene and protein expression of <i>DLX4</i> in cleft mucosa, although no differences in gene expression levels of <i>HOXB3</i> and <i>MSX2</i> were noted. However, a significant increase in protein expression for these genes was noted in the cleft mucosa (<i>p</i> < 0.05), indicating increased cellular proliferation. This was coupled with a significant increase in <i>NF-κB</i> protein expression in cleft mucosa (<i>p</i> < 0.05), highlighting the role of these genes in promotion of pro-inflammatory environment. Finally, no differences in gene expression of <i>PTX3</i> were noted.Nityanand JainMara PilmaneMDPI AGarticlecleft lip and palateinflammationimmunohistochemistryin-situ hybridization<i>HOXB3</i><i>DLX4</i>MedicineRENJournal of Personalized Medicine, Vol 11, Iss 1135, p 1135 (2021)
institution DOAJ
collection DOAJ
language EN
topic cleft lip and palate
inflammation
immunohistochemistry
in-situ hybridization
<i>HOXB3</i>
<i>DLX4</i>
Medicine
R
spellingShingle cleft lip and palate
inflammation
immunohistochemistry
in-situ hybridization
<i>HOXB3</i>
<i>DLX4</i>
Medicine
R
Nityanand Jain
Mara Pilmane
Evaluating the Expression of Candidate Homeobox Genes and Their Role in Local-Site Inflammation in Mucosal Tissue Obtained from Children with Non-Syndromic Cleft Lip and Palate
description Craniofacial development including palatogenesis is a complex process which requires an orchestrated and spatiotemporal expression of various genes and factors for proper embryogenesis and organogenesis. One such group of genes essential for craniofacial development is the homeobox genes, transcriptional factors that are commonly associated with congenital abnormalities. Amongst these genes, <i>DLX4, HOXB3,</i> and <i>MSX2</i> have been recently shown to be involved in the etiology of non-syndromic cleft lip and palate. Hence, we investigated the gene and protein expression of these genes in normal and cleft affected mucosal tissue obtained from 22 children, along with analyzing their role in promoting local-site inflammation using <i>NF-κB</i>. Additionally, we investigated the role of <i>PTX3,</i> which plays a critical role in tissue remodeling and wound repair. We found a residual gene and protein expression of <i>DLX4</i> in cleft mucosa, although no differences in gene expression levels of <i>HOXB3</i> and <i>MSX2</i> were noted. However, a significant increase in protein expression for these genes was noted in the cleft mucosa (<i>p</i> < 0.05), indicating increased cellular proliferation. This was coupled with a significant increase in <i>NF-κB</i> protein expression in cleft mucosa (<i>p</i> < 0.05), highlighting the role of these genes in promotion of pro-inflammatory environment. Finally, no differences in gene expression of <i>PTX3</i> were noted.
format article
author Nityanand Jain
Mara Pilmane
author_facet Nityanand Jain
Mara Pilmane
author_sort Nityanand Jain
title Evaluating the Expression of Candidate Homeobox Genes and Their Role in Local-Site Inflammation in Mucosal Tissue Obtained from Children with Non-Syndromic Cleft Lip and Palate
title_short Evaluating the Expression of Candidate Homeobox Genes and Their Role in Local-Site Inflammation in Mucosal Tissue Obtained from Children with Non-Syndromic Cleft Lip and Palate
title_full Evaluating the Expression of Candidate Homeobox Genes and Their Role in Local-Site Inflammation in Mucosal Tissue Obtained from Children with Non-Syndromic Cleft Lip and Palate
title_fullStr Evaluating the Expression of Candidate Homeobox Genes and Their Role in Local-Site Inflammation in Mucosal Tissue Obtained from Children with Non-Syndromic Cleft Lip and Palate
title_full_unstemmed Evaluating the Expression of Candidate Homeobox Genes and Their Role in Local-Site Inflammation in Mucosal Tissue Obtained from Children with Non-Syndromic Cleft Lip and Palate
title_sort evaluating the expression of candidate homeobox genes and their role in local-site inflammation in mucosal tissue obtained from children with non-syndromic cleft lip and palate
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/ce0042b92db24c409f95a16e5af6e644
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AT marapilmane evaluatingtheexpressionofcandidatehomeoboxgenesandtheirroleinlocalsiteinflammationinmucosaltissueobtainedfromchildrenwithnonsyndromiccleftlipandpalate
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