Metallothioneins in Dental Implant Treatment Failure and Periodontitis in Patients with Down’s Syndrome: Validation of Results

Metallothioneins (MTs) are low molecular weight cysteine-rich proteins that can bind up to seven zinc ions. Among their numerous functions, MTs appear to act as protectors against oxidative and inflammatory injury. In our first published study, we reported downregulation of the isoforms <i>MT1...

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Main Authors: María Baus-Domínguez, Raquel Gómez-Díaz, José-Luis Gutiérrez-Pérez, Daniel Torres-Lagares, Guillermo Machuca-Portillo, María-Ángeles Serrera-Figallo
Format: Article
Language:English
Published: MDPI AG 2022-06-01
Series:Genes
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Online Access:https://www.mdpi.com/2073-4425/13/6/1028
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author María Baus-Domínguez
Raquel Gómez-Díaz
José-Luis Gutiérrez-Pérez
Daniel Torres-Lagares
Guillermo Machuca-Portillo
María-Ángeles Serrera-Figallo
author_facet María Baus-Domínguez
Raquel Gómez-Díaz
José-Luis Gutiérrez-Pérez
Daniel Torres-Lagares
Guillermo Machuca-Portillo
María-Ángeles Serrera-Figallo
author_sort María Baus-Domínguez
collection DOAJ
description Metallothioneins (MTs) are low molecular weight cysteine-rich proteins that can bind up to seven zinc ions. Among their numerous functions, MTs appear to act as protectors against oxidative and inflammatory injury. In our first published study, we reported downregulation of the isoforms <i>MT1B</i> (fold distance (FD) −2. 95; <i>p</i> = 0.0024), <i>MT1F</i> (FD −1.72; <i>p</i> = 0.0276), <i>MT1X</i> (FD −3.09; <i>p</i> = 0.0021), <i>MT1H</i> (FD −2.39; <i>p</i> = 0.0018), <i>MT1M</i> (FD −2.37; <i>p</i> = 0.0092), <i>MT1L</i> (FD −2. 55; <i>p</i> = 0.0048), <i>MT1E</i> (FD −2.71; <i>p</i> = 0.0014), <i>MT2A</i> (FD −2.35; <i>p</i> = 0.0072), <i>MT1G</i> (FD −2.24; <i>p</i> = 0.0118), and <i>MT1A</i> (FD −2.82; <i>p</i> = 0.0023) by comparing Down’s syndrome patients with periodontal disease and implant failure to those without periodontal disease and with a positive progression of their implants. In this gene validation study, we intended to verify the results of our first gene expression analysis. Materials and Methods: In our retrospective case–control study, we performed retrotranscription (RT-qPCR) of 11 RNA-to-cDNA samples using the SuperScript™ VILO™ kit (50; reference 1,176,605) from Thermo Fisher. We conducted the study using the real-time PCR technique on the q-PCR ViiA 7 platform from Thermo Fisher. We chose the format of the Taqman Array Plate 16 Plus (reference 4,413,261) from Thermo Fisher, which accommodates 12 genes plus four controls (<i>GAPDH, 18S, ACTB,</i> and <i>HPRT1</i>). We conducted the analysis of the plates using the Thermo Fisher Cloud Web Software. Results: The results obtained through gene validation analysis show that in PD+RI+ patients, the genes encoding the isoforms <i>MT1F</i> (FD 0.3; <i>p</i> = 0.039), <i>MT1X</i> (FD 338; <i>p</i> = 0.0078), <i>MT1E</i> (FD 307; <i>p</i> = 0.0358), and <i>MT2A</i> (FD 252; <i>p</i> = 0.0428) continue to show downregulation, whereas <i>MT1B</i> (FD 2.75; <i>p</i> = 0.580), <i>MT1H</i> (FD 281; <i>p</i> = 0.152), <i>MT1L</i> (FD 354; <i>p</i> = 0.0965), and <i>MT1G</i> (FD 336; <i>p</i> = 0.0749) no longer show statistically significant results.
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spelling doaj.art-a4f12fd816dd42a1a16fefc1d447605d2023-11-23T16:48:06ZengMDPI AGGenes2073-44252022-06-01136102810.3390/genes13061028Metallothioneins in Dental Implant Treatment Failure and Periodontitis in Patients with Down’s Syndrome: Validation of ResultsMaría Baus-Domínguez0Raquel Gómez-Díaz1José-Luis Gutiérrez-Pérez2Daniel Torres-Lagares3Guillermo Machuca-Portillo4María-Ángeles Serrera-Figallo5Department of Dentistry, Faculty of Dentistry, University of Seville, 41009 Seville, SpainInstitute of Biomedicine of Seville, 41013 Seville, SpainOral and Maxillofacial Unit, Virgen del Rocio Hospital, 41013 Seville, SpainDepartment of Dentistry, Faculty of Dentistry, University of Seville, 41009 Seville, SpainDepartment of Dentistry, Faculty of Dentistry, University of Seville, 41009 Seville, SpainDepartment of Dentistry, Faculty of Dentistry, University of Seville, 41009 Seville, SpainMetallothioneins (MTs) are low molecular weight cysteine-rich proteins that can bind up to seven zinc ions. Among their numerous functions, MTs appear to act as protectors against oxidative and inflammatory injury. In our first published study, we reported downregulation of the isoforms <i>MT1B</i> (fold distance (FD) −2. 95; <i>p</i> = 0.0024), <i>MT1F</i> (FD −1.72; <i>p</i> = 0.0276), <i>MT1X</i> (FD −3.09; <i>p</i> = 0.0021), <i>MT1H</i> (FD −2.39; <i>p</i> = 0.0018), <i>MT1M</i> (FD −2.37; <i>p</i> = 0.0092), <i>MT1L</i> (FD −2. 55; <i>p</i> = 0.0048), <i>MT1E</i> (FD −2.71; <i>p</i> = 0.0014), <i>MT2A</i> (FD −2.35; <i>p</i> = 0.0072), <i>MT1G</i> (FD −2.24; <i>p</i> = 0.0118), and <i>MT1A</i> (FD −2.82; <i>p</i> = 0.0023) by comparing Down’s syndrome patients with periodontal disease and implant failure to those without periodontal disease and with a positive progression of their implants. In this gene validation study, we intended to verify the results of our first gene expression analysis. Materials and Methods: In our retrospective case–control study, we performed retrotranscription (RT-qPCR) of 11 RNA-to-cDNA samples using the SuperScript™ VILO™ kit (50; reference 1,176,605) from Thermo Fisher. We conducted the study using the real-time PCR technique on the q-PCR ViiA 7 platform from Thermo Fisher. We chose the format of the Taqman Array Plate 16 Plus (reference 4,413,261) from Thermo Fisher, which accommodates 12 genes plus four controls (<i>GAPDH, 18S, ACTB,</i> and <i>HPRT1</i>). We conducted the analysis of the plates using the Thermo Fisher Cloud Web Software. Results: The results obtained through gene validation analysis show that in PD+RI+ patients, the genes encoding the isoforms <i>MT1F</i> (FD 0.3; <i>p</i> = 0.039), <i>MT1X</i> (FD 338; <i>p</i> = 0.0078), <i>MT1E</i> (FD 307; <i>p</i> = 0.0358), and <i>MT2A</i> (FD 252; <i>p</i> = 0.0428) continue to show downregulation, whereas <i>MT1B</i> (FD 2.75; <i>p</i> = 0.580), <i>MT1H</i> (FD 281; <i>p</i> = 0.152), <i>MT1L</i> (FD 354; <i>p</i> = 0.0965), and <i>MT1G</i> (FD 336; <i>p</i> = 0.0749) no longer show statistically significant results.https://www.mdpi.com/2073-4425/13/6/1028Down’s syndromeperiodontal diseasebone biologyclinical outcomesgene expressionvalidation
spellingShingle María Baus-Domínguez
Raquel Gómez-Díaz
José-Luis Gutiérrez-Pérez
Daniel Torres-Lagares
Guillermo Machuca-Portillo
María-Ángeles Serrera-Figallo
Metallothioneins in Dental Implant Treatment Failure and Periodontitis in Patients with Down’s Syndrome: Validation of Results
Genes
Down’s syndrome
periodontal disease
bone biology
clinical outcomes
gene expression
validation
title Metallothioneins in Dental Implant Treatment Failure and Periodontitis in Patients with Down’s Syndrome: Validation of Results
title_full Metallothioneins in Dental Implant Treatment Failure and Periodontitis in Patients with Down’s Syndrome: Validation of Results
title_fullStr Metallothioneins in Dental Implant Treatment Failure and Periodontitis in Patients with Down’s Syndrome: Validation of Results
title_full_unstemmed Metallothioneins in Dental Implant Treatment Failure and Periodontitis in Patients with Down’s Syndrome: Validation of Results
title_short Metallothioneins in Dental Implant Treatment Failure and Periodontitis in Patients with Down’s Syndrome: Validation of Results
title_sort metallothioneins in dental implant treatment failure and periodontitis in patients with down s syndrome validation of results
topic Down’s syndrome
periodontal disease
bone biology
clinical outcomes
gene expression
validation
url https://www.mdpi.com/2073-4425/13/6/1028
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