Cargando…

Aberrant UBR4 expressions in Hirschsprung disease patients

BACKGROUND: Recently, pathogenic alleles within ubiquitin N-recognin domain-containing E3 ligase 4 (UBR4) gene have been shown to be associated with Hirschsprung disease (HSCR). We determined the UBR4 expressions in Indonesian HSCR patients. METHODS: We analyzed the UBR4 expressions in the colons of...

Descripción completa

Detalles Bibliográficos
Autores principales: Gunadi, Kalim, Alvin Santoso, Liana, Estelita, Fauzi, Aditya Rifqi, Sirait, Dian Nirmala, Afandy, Dwiki, Kencana, Sagita Mega Sekar, Purnomo, Eko, Iskandar, Kristy, Makhmudi, Akhmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907357/
https://www.ncbi.nlm.nih.gov/pubmed/31830949
http://dx.doi.org/10.1186/s12887-019-1879-7
_version_ 1783478528873857024
author Gunadi
Kalim, Alvin Santoso
Liana, Estelita
Fauzi, Aditya Rifqi
Sirait, Dian Nirmala
Afandy, Dwiki
Kencana, Sagita Mega Sekar
Purnomo, Eko
Iskandar, Kristy
Makhmudi, Akhmad
author_facet Gunadi
Kalim, Alvin Santoso
Liana, Estelita
Fauzi, Aditya Rifqi
Sirait, Dian Nirmala
Afandy, Dwiki
Kencana, Sagita Mega Sekar
Purnomo, Eko
Iskandar, Kristy
Makhmudi, Akhmad
author_sort Gunadi
collection PubMed
description BACKGROUND: Recently, pathogenic alleles within ubiquitin N-recognin domain-containing E3 ligase 4 (UBR4) gene have been shown to be associated with Hirschsprung disease (HSCR). We determined the UBR4 expressions in Indonesian HSCR patients. METHODS: We analyzed the UBR4 expressions in the colons of HSCR patient and anorectal malformation (ARM) patient as control by real-time polymerase chain reaction (qPCR). RESULTS: Thirty-seven patients with non-syndromic HSCR and eighteen controls were involved in this study. qPCR revealed that the UBR4 expression was strongly decreased (0.77-fold) in the ganglionic group of patients with HSCR compared to the control group with ARM (ΔC(T) 2.43 ± 0.36 vs. 2.05 ± 0.69; p = 0.009), whereas the UBR4 expression was also significantly reduced (0.79-fold) in the aganglionic group of patients with HSCR compared to the control group with ARM (ΔC(T) 2.39 ± 0.46 vs. 2.05 ± 0.69; p = 0.044). However, the UBR4 expression change was not associated with gender (p = 0.35 and 0.80), nor with degree of aganglionosis both in ganglionic and aganglionic colons (p = 0.72 and 0.73), respectively. CONCLUSION: Our study demonstrates that expression of UBR4 is decreased in both aganglionic and ganglionic colon of HSCR patients.
format Online
Article
Text
id pubmed-6907357
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-69073572019-12-19 Aberrant UBR4 expressions in Hirschsprung disease patients Gunadi Kalim, Alvin Santoso Liana, Estelita Fauzi, Aditya Rifqi Sirait, Dian Nirmala Afandy, Dwiki Kencana, Sagita Mega Sekar Purnomo, Eko Iskandar, Kristy Makhmudi, Akhmad BMC Pediatr Research Article BACKGROUND: Recently, pathogenic alleles within ubiquitin N-recognin domain-containing E3 ligase 4 (UBR4) gene have been shown to be associated with Hirschsprung disease (HSCR). We determined the UBR4 expressions in Indonesian HSCR patients. METHODS: We analyzed the UBR4 expressions in the colons of HSCR patient and anorectal malformation (ARM) patient as control by real-time polymerase chain reaction (qPCR). RESULTS: Thirty-seven patients with non-syndromic HSCR and eighteen controls were involved in this study. qPCR revealed that the UBR4 expression was strongly decreased (0.77-fold) in the ganglionic group of patients with HSCR compared to the control group with ARM (ΔC(T) 2.43 ± 0.36 vs. 2.05 ± 0.69; p = 0.009), whereas the UBR4 expression was also significantly reduced (0.79-fold) in the aganglionic group of patients with HSCR compared to the control group with ARM (ΔC(T) 2.39 ± 0.46 vs. 2.05 ± 0.69; p = 0.044). However, the UBR4 expression change was not associated with gender (p = 0.35 and 0.80), nor with degree of aganglionosis both in ganglionic and aganglionic colons (p = 0.72 and 0.73), respectively. CONCLUSION: Our study demonstrates that expression of UBR4 is decreased in both aganglionic and ganglionic colon of HSCR patients. BioMed Central 2019-12-12 /pmc/articles/PMC6907357/ /pubmed/31830949 http://dx.doi.org/10.1186/s12887-019-1879-7 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Gunadi
Kalim, Alvin Santoso
Liana, Estelita
Fauzi, Aditya Rifqi
Sirait, Dian Nirmala
Afandy, Dwiki
Kencana, Sagita Mega Sekar
Purnomo, Eko
Iskandar, Kristy
Makhmudi, Akhmad
Aberrant UBR4 expressions in Hirschsprung disease patients
title Aberrant UBR4 expressions in Hirschsprung disease patients
title_full Aberrant UBR4 expressions in Hirschsprung disease patients
title_fullStr Aberrant UBR4 expressions in Hirschsprung disease patients
title_full_unstemmed Aberrant UBR4 expressions in Hirschsprung disease patients
title_short Aberrant UBR4 expressions in Hirschsprung disease patients
title_sort aberrant ubr4 expressions in hirschsprung disease patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907357/
https://www.ncbi.nlm.nih.gov/pubmed/31830949
http://dx.doi.org/10.1186/s12887-019-1879-7
work_keys_str_mv AT gunadi aberrantubr4expressionsinhirschsprungdiseasepatients
AT kalimalvinsantoso aberrantubr4expressionsinhirschsprungdiseasepatients
AT lianaestelita aberrantubr4expressionsinhirschsprungdiseasepatients
AT fauziadityarifqi aberrantubr4expressionsinhirschsprungdiseasepatients
AT siraitdiannirmala aberrantubr4expressionsinhirschsprungdiseasepatients
AT afandydwiki aberrantubr4expressionsinhirschsprungdiseasepatients
AT kencanasagitamegasekar aberrantubr4expressionsinhirschsprungdiseasepatients
AT purnomoeko aberrantubr4expressionsinhirschsprungdiseasepatients
AT iskandarkristy aberrantubr4expressionsinhirschsprungdiseasepatients
AT makhmudiakhmad aberrantubr4expressionsinhirschsprungdiseasepatients