Methylation pattern of IFN-γ and IL-10 genes in periodontal tissues
DNA methylation is characterized by the addition of methyl groups in cytosines within CpG islands. Unmethylated CpGs are related to transcriptionally active structure, whereas methylated CpG recruits methyl-binding proteins that promote chromatin compaction. DNA methylation can influence the express...
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Published in | Immunobiology (1979) Vol. 216; no. 8; pp. 936 - 941 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier GmbH
01.08.2011
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ISSN | 0171-2985 1878-3279 1878-3279 |
DOI | 10.1016/j.imbio.2011.01.006 |
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Abstract | DNA methylation is characterized by the addition of methyl groups in cytosines within CpG islands. Unmethylated CpGs are related to transcriptionally active structure, whereas methylated CpG recruits methyl-binding proteins that promote chromatin compaction. DNA methylation can influence the expression of cytokines and affect the development of periodontal disease.
The purpose of the present study was to evaluate the methylation status of the interferon gamma (IFN-γ) and interleukin-10 (IL-10) genes in periodontal tissues.
Methylation-specific polymerase chain reaction (MSP) and DNA sequencing analysis were used to verify the DNA methylation status of the IFN-γ and IL-10 genes, respectively, in samples from subjects without periodontitis and individuals with chronic periodontitis. Histological sections stained by hematoxylin–eosin were used for histopathological evaluation of samples.
The methylation status of the IFN-γ and IL-10 genes was similar among the groups. Most of the samples were positive for IFN-γ methylation. Only 11% of the periodontitis group showed unmethylated DNA. Considering the IL-10 gene, no unmethylated sample was observed. The profile of total or partial methylation was detected in CpGs evaluated.
The results showed evidence that methylation of IFN-γ and IL-10 genes is a usual feature on periodontal tissues. Further studies are needed to determine the functional relevance of these alterations. |
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AbstractList | DNA methylation is characterized by the addition of methyl groups in cytosines within CpG islands. Unmethylated CpGs are related to transcriptionally active structure, whereas methylated CpG recruits methyl-binding proteins that promote chromatin compaction. DNA methylation can influence the expression of cytokines and affect the development of periodontal disease.UNLABELLEDDNA methylation is characterized by the addition of methyl groups in cytosines within CpG islands. Unmethylated CpGs are related to transcriptionally active structure, whereas methylated CpG recruits methyl-binding proteins that promote chromatin compaction. DNA methylation can influence the expression of cytokines and affect the development of periodontal disease.The purpose of the present study was to evaluate the methylation status of the interferon gamma (IFN-γ) and interleukin-10 (IL-10) genes in periodontal tissues.OBJECTIVESThe purpose of the present study was to evaluate the methylation status of the interferon gamma (IFN-γ) and interleukin-10 (IL-10) genes in periodontal tissues.Methylation-specific polymerase chain reaction (MSP) and DNA sequencing analysis were used to verify the DNA methylation status of the IFN-γ and IL-10 genes, respectively, in samples from subjects without periodontitis and individuals with chronic periodontitis. Histological sections stained by hematoxylin-eosin were used for histopathological evaluation of samples.DESIGNMethylation-specific polymerase chain reaction (MSP) and DNA sequencing analysis were used to verify the DNA methylation status of the IFN-γ and IL-10 genes, respectively, in samples from subjects without periodontitis and individuals with chronic periodontitis. Histological sections stained by hematoxylin-eosin were used for histopathological evaluation of samples.The methylation status of the IFN-γ and IL-10 genes was similar among the groups. Most of the samples were positive for IFN-γ methylation. Only 11% of the periodontitis group showed unmethylated DNA. Considering the IL-10 gene, no unmethylated sample was observed. The profile of total or partial methylation was detected in CpGs evaluated.RESULTSThe methylation status of the IFN-γ and IL-10 genes was similar among the groups. Most of the samples were positive for IFN-γ methylation. Only 11% of the periodontitis group showed unmethylated DNA. Considering the IL-10 gene, no unmethylated sample was observed. The profile of total or partial methylation was detected in CpGs evaluated.The results showed evidence that methylation of IFN-γ and IL-10 genes is a usual feature on periodontal tissues. Further studies are needed to determine the functional relevance of these alterations.CONCLUSIONSThe results showed evidence that methylation of IFN-γ and IL-10 genes is a usual feature on periodontal tissues. Further studies are needed to determine the functional relevance of these alterations. DNA methylation is characterized by the addition of methyl groups in cytosines within CpG islands. Unmethylated CpGs are related to transcriptionally active structure, whereas methylated CpG recruits methyl-binding proteins that promote chromatin compaction. DNA methylation can influence the expression of cytokines and affect the development of periodontal disease. The purpose of the present study was to evaluate the methylation status of the interferon gamma (IFN-γ) and interleukin-10 (IL-10) genes in periodontal tissues. Methylation-specific polymerase chain reaction (MSP) and DNA sequencing analysis were used to verify the DNA methylation status of the IFN-γ and IL-10 genes, respectively, in samples from subjects without periodontitis and individuals with chronic periodontitis. Histological sections stained by hematoxylin–eosin were used for histopathological evaluation of samples. The methylation status of the IFN-γ and IL-10 genes was similar among the groups. Most of the samples were positive for IFN-γ methylation. Only 11% of the periodontitis group showed unmethylated DNA. Considering the IL-10 gene, no unmethylated sample was observed. The profile of total or partial methylation was detected in CpGs evaluated. The results showed evidence that methylation of IFN-γ and IL-10 genes is a usual feature on periodontal tissues. Further studies are needed to determine the functional relevance of these alterations. DNA methylation is characterized by the addition of methyl groups in cytosines within CpG islands. Unmethylated CpGs are related to transcriptionally active structure, whereas methylated CpG recruits methyl-binding proteins that promote chromatin compaction. DNA methylation can influence the expression of cytokines and affect the development of periodontal disease. Objectives: The purpose of the present study was to evaluate the methylation status of the interferon gamma (IFN- gamma ) and interleukin-10 (IL-10) genes in periodontal tissues. Design: Methylation-specific polymerase chain reaction (MSP) and DNA sequencing analysis were used to verify the DNA methylation status of the IFN- gamma and IL-10 genes, respectively, in samples from subjects without periodontitis and individuals with chronic periodontitis. Histological sections stained by hematoxylin-eosin were used for histopathological evaluation of samples. Results: The methylation status of the IFN- gamma and IL-10 genes was similar among the groups. Most of the samples were positive for IFN- gamma methylation. Only 11% of the periodontitis group showed unmethylated DNA. Considering the IL-10 gene, no unmethylated sample was observed. The profile of total or partial methylation was detected in CpGs evaluated. Conclusions: The results showed evidence that methylation of IFN- gamma and IL-10 genes is a usual feature on periodontal tissues. Further studies are needed to determine the functional relevance of these alterations. Abstract DNA methylation is characterized by the addition of methyl groups in cytosines within CpG islands. Unmethylated CpGs are related to transcriptionally active structure, whereas methylated CpG recruits methyl-binding proteins that promote chromatin compaction. DNA methylation can influence the expression of cytokines and affect the development of periodontal disease. Objectives The purpose of the present study was to evaluate the methylation status of the interferon gamma ( IFN-γ ) and interleukin-10 ( IL-10 ) genes in periodontal tissues. Design Methylation-specific polymerase chain reaction (MSP) and DNA sequencing analysis were used to verify the DNA methylation status of the IFN-γ and IL-10 genes, respectively, in samples from subjects without periodontitis and individuals with chronic periodontitis. Histological sections stained by hematoxylin–eosin were used for histopathological evaluation of samples. Results The methylation status of the IFN-γ and IL-10 genes was similar among the groups. Most of the samples were positive for IFN-γ methylation. Only 11% of the periodontitis group showed unmethylated DNA. Considering the IL-10 gene, no unmethylated sample was observed. The profile of total or partial methylation was detected in CpGs evaluated. Conclusions The results showed evidence that methylation of IFN-γ and IL-10 genes is a usual feature on periodontal tissues. Further studies are needed to determine the functional relevance of these alterations. |
Author | Viana, Michelle Beatriz Diniz, Marina Gonçalves Costa, Fernando Oliveira Gomez, Ricardo Santiago Moreira, Paula Rocha da Costa, José Eustáquio Cardoso, Fabiano Pereira |
Author_xml | – sequence: 1 givenname: Michelle Beatriz surname: Viana fullname: Viana, Michelle Beatriz organization: Laboratory of Molecular Biology, Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil – sequence: 2 givenname: Fabiano Pereira surname: Cardoso fullname: Cardoso, Fabiano Pereira organization: Laboratory of Molecular Biology, Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil – sequence: 3 givenname: Marina Gonçalves surname: Diniz fullname: Diniz, Marina Gonçalves organization: Laboratory of Molecular Biology, Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil – sequence: 4 givenname: Fernando Oliveira surname: Costa fullname: Costa, Fernando Oliveira organization: Department of Periodontology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil – sequence: 5 givenname: José Eustáquio surname: da Costa fullname: da Costa, José Eustáquio organization: Department of Periodontology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil – sequence: 6 givenname: Ricardo Santiago surname: Gomez fullname: Gomez, Ricardo Santiago organization: Laboratory of Molecular Biology, Department of Oral Surgery and Pathology, School of Dentistry, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil – sequence: 7 givenname: Paula Rocha surname: Moreira fullname: Moreira, Paula Rocha email: paularocha2003@yahoo.com.br organization: Laboratory of Cell-Cell Interactions, Department of Morphology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Avenida Antônio Carlos 6627, CEP 31.270-901, Belo Horizonte, Minas Gerais, Brazil |
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Cites_doi | 10.1902/jop.2010.100082 10.1177/154411130301400605 10.1038/ncponc0354 10.1016/j.leukres.2005.04.012 10.1007/s10875-007-9148-1 10.1902/annals.1999.4.1.1 10.1111/j.1600-051X.2005.00821.x 10.1006/bbrc.1999.0566 10.1111/j.1600-0757.1997.tb00199.x 10.1186/1479-5876-8-110 10.1046/j.1365-2249.2001.01448.x 10.1001/archotol.130.1.39 10.1111/j.1600-0757.2006.00188.x 10.1016/S1521-6616(03)00206-7 10.1016/j.ejca.2008.02.046 10.1111/j.1600-051X.2010.01616.x 10.1902/jop.2008.080172 10.1111/j.1600-0757.1997.tb00194.x 10.1177/154405910708600212 10.1016/j.coi.2007.07.016 10.1902/jop.2008.080220 10.1016/j.molimm.2005.11.010 10.1111/j.1600-051X.2009.01446.x 10.1177/0022034509356512 10.1034/j.1600-0765.2003.02012.x 10.4049/jimmunol.165.7.3626 10.1189/jlb.1004604 |
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References | Offenbacher, Barros, Beck (bib0095) 2008; 79 Wilson (bib0125) 2008; 79 Adcock, Tsaprouni, Bhavsar, Ito (bib0005) 2009; 19 Ishikawa (bib0065) 2007; 43 Kwon, Kim, Lee, Oh, Choi (bib0075) 2008; 28 Madianos, Bobetsis, Kinane (bib0090) 2005; 32 Richardson (bib0110) 2003; 109 Page (bib0105) 1997; 14 Gopissetty, Ramachandram, Singal (bib0060) 2006; 43 Szalmás, Bánáti, Koroknai, László, Fehér, Salamon, Gergely, Minárovits, Kónya (bib0120) 2008; 44 Andia, de Oliveira, Casarin, Casati, Line, de Souza (bib0010) 2010; 81 Baylin (bib0025) 2005; 2 Goldenberg, Harden, Masayesva, Há, Benoit, Westra, Koch, Sidransky, Califano (bib0055) 2004; 130 Sasaki, Hou, Belani, Wang, Uchiyama, Müller, Stashenko (bib0115) 2000; 165 Zhang, Crivello, Offenbacher, Moretti, Paquette, Barros (bib0135) 2010; 37 Loo, Jin, Cheung, Wang, Chow (bib0085) 2010; 8 Kinane, Hart (bib0070) 2003; 14 Oliveira, Damm, Andia, Salmon, Nociti, Line, de Souza (bib0100) 2009; 36 Armenante, Merola, Furia, Palmiere (bib0015) 1999; 258 Armitage (bib0020) 1999; 4 Bobetsis, Barros, Lin, Weidman, Dolinoy, Jirtle, Boggess, Beck, Offenbacher (bib0030) 2007; 86 Brakensiek, Länger, Kreipe, Lehmann (bib0040) 2005; 29 Gemmel, Marshall, Seymour (bib0050) 1997; 14 Garlet, Martins, Ferreira, Milanezi, Silva (bib0045) 2003; 38 Lappin, Macleod, Kerr, Mitchell, Kinane (bib0080) 2001; 123 Bonilla-Henao, Martínez, Sobrino, Pintado (bib0035) 2005; 78 Zhang, Barros, Niculescu, Moretti, Preisser, Offenbacher (bib0130) 2010; 89 Garlet (10.1016/j.imbio.2011.01.006_bib0045) 2003; 38 Oliveira (10.1016/j.imbio.2011.01.006_bib0100) 2009; 36 Kwon (10.1016/j.imbio.2011.01.006_bib0075) 2008; 28 Adcock (10.1016/j.imbio.2011.01.006_bib0005) 2009; 19 Armenante (10.1016/j.imbio.2011.01.006_bib0015) 1999; 258 Brakensiek (10.1016/j.imbio.2011.01.006_bib0040) 2005; 29 Lappin (10.1016/j.imbio.2011.01.006_bib0080) 2001; 123 Zhang (10.1016/j.imbio.2011.01.006_bib0130) 2010; 89 Zhang (10.1016/j.imbio.2011.01.006_bib0135) 2010; 37 Goldenberg (10.1016/j.imbio.2011.01.006_bib0055) 2004; 130 Richardson (10.1016/j.imbio.2011.01.006_bib0110) 2003; 109 Gopissetty (10.1016/j.imbio.2011.01.006_bib0060) 2006; 43 Offenbacher (10.1016/j.imbio.2011.01.006_bib0095) 2008; 79 Szalmás (10.1016/j.imbio.2011.01.006_bib0120) 2008; 44 Page (10.1016/j.imbio.2011.01.006_bib0105) 1997; 14 Andia (10.1016/j.imbio.2011.01.006_bib0010) 2010; 81 Armitage (10.1016/j.imbio.2011.01.006_bib0020) 1999; 4 Loo (10.1016/j.imbio.2011.01.006_bib0085) 2010; 8 Wilson (10.1016/j.imbio.2011.01.006_bib0125) 2008; 79 Bobetsis (10.1016/j.imbio.2011.01.006_bib0030) 2007; 86 Sasaki (10.1016/j.imbio.2011.01.006_bib0115) 2000; 165 Madianos (10.1016/j.imbio.2011.01.006_bib0090) 2005; 32 Ishikawa (10.1016/j.imbio.2011.01.006_bib0065) 2007; 43 Kinane (10.1016/j.imbio.2011.01.006_bib0070) 2003; 14 Baylin (10.1016/j.imbio.2011.01.006_bib0025) 2005; 2 Gemmel (10.1016/j.imbio.2011.01.006_bib0050) 1997; 14 Bonilla-Henao (10.1016/j.imbio.2011.01.006_bib0035) 2005; 78 |
References_xml | – volume: 36 start-page: 719 year: 2009 end-page: 725 ident: bib0100 article-title: DNA methylation status of IL-8 gene promoter in oral cells of smokers and nonsmokers with chronic periodontitis publication-title: J. Clin. Periodontol. – volume: 38 start-page: 210 year: 2003 end-page: 217 ident: bib0045 article-title: Patterns of chemokine receptors expression in different forms of human periodontal disease publication-title: J. Periodontol. Res. – volume: 81 start-page: 1336 year: 2010 end-page: 1341 ident: bib0010 article-title: DNA methylation status of the IL-8 gene promoter in aggressive periodontitis publication-title: J. Periodontol. – volume: 130 start-page: 39 year: 2004 end-page: 44 ident: bib0055 article-title: Intraoperative molecular margin analysis in head and neck cancer publication-title: Arch. Otolaryngol. Head Neck Surg. – volume: 2 start-page: 4 year: 2005 end-page: 11 ident: bib0025 article-title: DNA methylation and gene silencing in cancer publication-title: Nat. Clin. Pract. Oncol. – volume: 43 start-page: 1729 year: 2006 end-page: 1740 ident: bib0060 article-title: DNA methylation and apoptosis publication-title: Mol. Immunol. – volume: 79 start-page: 1577 year: 2008 end-page: 1584 ident: bib0095 article-title: Rethinking periodontal inflammation publication-title: J. Periodontol. – volume: 19 start-page: 694 year: 2009 end-page: 700 ident: bib0005 article-title: Epigenetic regulation of airway inflammation publication-title: Curr. Opin. Immunol. – volume: 14 start-page: 216 year: 1997 end-page: 248 ident: bib0105 article-title: Advances in the pathogenesis of periodontitis: summary of developments, clinical implications and future directions publication-title: Periodontol. 2000 – volume: 79 start-page: 1514 year: 2008 end-page: 1519 ident: bib0125 article-title: Epigenetic regulation in the inflammatory response and relevance to common diseases publication-title: J. Periodontol. – volume: 8 start-page: 110 year: 2010 ident: bib0085 article-title: Epigenetic change in E-cadherin and Cox-2 to predict chronic periodontitis publication-title: J. Trans. Med. – volume: 78 start-page: 1339 year: 2005 end-page: 1346 ident: bib0035 article-title: Different signaling pathways inhibit DNA methylation activity and up-regulated IFN-γ in human lymphocytes publication-title: J. Leukoc. Biol. – volume: 29 start-page: 1357 year: 2005 end-page: 1360 ident: bib0040 article-title: Absence of p21 (C1P1), p27 (KIP 1) and p57 (KIP2) methylation in MDS and AML publication-title: Leuk. Res. – volume: 89 start-page: 133 year: 2010 end-page: 137 ident: bib0130 article-title: Alteration of PTGS2 promoter methylation in chronic periodontitis publication-title: J. Dent. Res. – volume: 4 start-page: 1 year: 1999 end-page: 112 ident: bib0020 publication-title: International Workshop for a Classification of Periodontal Diseases and Conditions – volume: 43 start-page: 9 year: 2007 end-page: 13 ident: bib0065 article-title: Host responses in periodontal disease: a preview publication-title: Periodontol. 2000 – volume: 37 start-page: 953 year: 2010 end-page: 961 ident: bib0135 article-title: Interferon-gamma promoter hypomethylation and increased expression in chronic periodontitis publication-title: J. Clin. Periodontol. – volume: 44 start-page: 1030 year: 2008 end-page: 1038 ident: bib0120 article-title: Lineage-specifc silencing of human IL-10 expression by promoter methylation in cervical cancer cells publication-title: Eur. J. Cancer – volume: 258 start-page: 644 year: 1999 end-page: 647 ident: bib0015 article-title: Repression of the IL-6 gene is associated with hypermethylation publication-title: Biochem. Biophys. Res. Commun. – volume: 14 start-page: 112 year: 1997 end-page: 143 ident: bib0050 article-title: Cytokines and prostaglandinsin immune homeostasis and tissue destruction in periodontal disease publication-title: Periodontol. 2000 – volume: 14 start-page: 430 year: 2003 end-page: 449 ident: bib0070 article-title: Genes and gene polymorphisms associated with periodontal disease publication-title: Crit. Rev. Oral Biol. Med. – volume: 32 start-page: 57 year: 2005 end-page: 71 ident: bib0090 article-title: Generation of inflammatory stimuli: how bacteria set up inflammatory responses in the gingiva publication-title: J. Clin. Periodontol. – volume: 123 start-page: 294 year: 2001 end-page: 300 ident: bib0080 article-title: Anti-inflammtory cytokine IL-10 and T cell cytokine profile in periodotitis granulation tissue publication-title: Clin. Exp. Immunol. – volume: 28 start-page: 139 year: 2008 end-page: 146 ident: bib0075 article-title: DNA methylation and expression of IL-4 and IFN-g gene promoter genes in patients with bronchial asthma publication-title: J. Clin. Immunol. – volume: 165 start-page: 3626 year: 2000 end-page: 3630 ident: bib0115 article-title: IL-10 but not IL-4, suppresses infection-stimulated bone resorption in vivo publication-title: J. Immunol. – volume: 86 start-page: 169 year: 2007 end-page: 174 ident: bib0030 article-title: Bacterial infection promotes DNA hypermethylation publication-title: J. Dent. Res. – volume: 109 start-page: 72 year: 2003 end-page: 79 ident: bib0110 article-title: DNA methylation and auto imune disease publication-title: Clin. Immunol. – volume: 81 start-page: 1336 issue: 9 year: 2010 ident: 10.1016/j.imbio.2011.01.006_bib0010 article-title: DNA methylation status of the IL-8 gene promoter in aggressive periodontitis publication-title: J. Periodontol. doi: 10.1902/jop.2010.100082 – volume: 14 start-page: 430 year: 2003 ident: 10.1016/j.imbio.2011.01.006_bib0070 article-title: Genes and gene polymorphisms associated with periodontal disease publication-title: Crit. Rev. Oral Biol. Med. doi: 10.1177/154411130301400605 – volume: 2 start-page: 4 issue: Suppl. 1 year: 2005 ident: 10.1016/j.imbio.2011.01.006_bib0025 article-title: DNA methylation and gene silencing in cancer publication-title: Nat. Clin. Pract. Oncol. doi: 10.1038/ncponc0354 – volume: 29 start-page: 1357 year: 2005 ident: 10.1016/j.imbio.2011.01.006_bib0040 article-title: Absence of p21 (C1P1), p27 (KIP 1) and p57 (KIP2) methylation in MDS and AML publication-title: Leuk. Res. doi: 10.1016/j.leukres.2005.04.012 – volume: 28 start-page: 139 year: 2008 ident: 10.1016/j.imbio.2011.01.006_bib0075 article-title: DNA methylation and expression of IL-4 and IFN-g gene promoter genes in patients with bronchial asthma publication-title: J. Clin. Immunol. doi: 10.1007/s10875-007-9148-1 – volume: 4 start-page: 1 year: 1999 ident: 10.1016/j.imbio.2011.01.006_bib0020 publication-title: Ann. Periodontol. doi: 10.1902/annals.1999.4.1.1 – volume: 32 start-page: 57 issue: Suppl. 6 year: 2005 ident: 10.1016/j.imbio.2011.01.006_bib0090 article-title: Generation of inflammatory stimuli: how bacteria set up inflammatory responses in the gingiva publication-title: J. Clin. Periodontol. doi: 10.1111/j.1600-051X.2005.00821.x – volume: 258 start-page: 644 issue: 3 year: 1999 ident: 10.1016/j.imbio.2011.01.006_bib0015 article-title: Repression of the IL-6 gene is associated with hypermethylation publication-title: Biochem. Biophys. Res. Commun. doi: 10.1006/bbrc.1999.0566 – volume: 14 start-page: 216 issue: 1 year: 1997 ident: 10.1016/j.imbio.2011.01.006_bib0105 article-title: Advances in the pathogenesis of periodontitis: summary of developments, clinical implications and future directions publication-title: Periodontol. 2000 doi: 10.1111/j.1600-0757.1997.tb00199.x – volume: 8 start-page: 110 year: 2010 ident: 10.1016/j.imbio.2011.01.006_bib0085 article-title: Epigenetic change in E-cadherin and Cox-2 to predict chronic periodontitis publication-title: J. Trans. Med. doi: 10.1186/1479-5876-8-110 – volume: 123 start-page: 294 year: 2001 ident: 10.1016/j.imbio.2011.01.006_bib0080 article-title: Anti-inflammtory cytokine IL-10 and T cell cytokine profile in periodotitis granulation tissue publication-title: Clin. Exp. Immunol. doi: 10.1046/j.1365-2249.2001.01448.x – volume: 130 start-page: 39 year: 2004 ident: 10.1016/j.imbio.2011.01.006_bib0055 article-title: Intraoperative molecular margin analysis in head and neck cancer publication-title: Arch. Otolaryngol. Head Neck Surg. doi: 10.1001/archotol.130.1.39 – volume: 43 start-page: 9 year: 2007 ident: 10.1016/j.imbio.2011.01.006_bib0065 article-title: Host responses in periodontal disease: a preview publication-title: Periodontol. 2000 doi: 10.1111/j.1600-0757.2006.00188.x – volume: 109 start-page: 72 issue: 1 year: 2003 ident: 10.1016/j.imbio.2011.01.006_bib0110 article-title: DNA methylation and auto imune disease publication-title: Clin. Immunol. doi: 10.1016/S1521-6616(03)00206-7 – volume: 44 start-page: 1030 issue: 7 year: 2008 ident: 10.1016/j.imbio.2011.01.006_bib0120 article-title: Lineage-specifc silencing of human IL-10 expression by promoter methylation in cervical cancer cells publication-title: Eur. J. Cancer doi: 10.1016/j.ejca.2008.02.046 – volume: 37 start-page: 953 issue: 11 year: 2010 ident: 10.1016/j.imbio.2011.01.006_bib0135 article-title: Interferon-gamma promoter hypomethylation and increased expression in chronic periodontitis publication-title: J. Clin. Periodontol. doi: 10.1111/j.1600-051X.2010.01616.x – volume: 79 start-page: 1514 issue: 8 year: 2008 ident: 10.1016/j.imbio.2011.01.006_bib0125 article-title: Epigenetic regulation in the inflammatory response and relevance to common diseases publication-title: J. Periodontol. doi: 10.1902/jop.2008.080172 – volume: 14 start-page: 112 year: 1997 ident: 10.1016/j.imbio.2011.01.006_bib0050 article-title: Cytokines and prostaglandinsin immune homeostasis and tissue destruction in periodontal disease publication-title: Periodontol. 2000 doi: 10.1111/j.1600-0757.1997.tb00194.x – volume: 86 start-page: 169 year: 2007 ident: 10.1016/j.imbio.2011.01.006_bib0030 article-title: Bacterial infection promotes DNA hypermethylation publication-title: J. Dent. Res. doi: 10.1177/154405910708600212 – volume: 19 start-page: 694 year: 2009 ident: 10.1016/j.imbio.2011.01.006_bib0005 article-title: Epigenetic regulation of airway inflammation publication-title: Curr. Opin. Immunol. doi: 10.1016/j.coi.2007.07.016 – volume: 79 start-page: 1577 issue: 8 Suppl. year: 2008 ident: 10.1016/j.imbio.2011.01.006_bib0095 article-title: Rethinking periodontal inflammation publication-title: J. Periodontol. doi: 10.1902/jop.2008.080220 – volume: 43 start-page: 1729 year: 2006 ident: 10.1016/j.imbio.2011.01.006_bib0060 article-title: DNA methylation and apoptosis publication-title: Mol. Immunol. doi: 10.1016/j.molimm.2005.11.010 – volume: 36 start-page: 719 year: 2009 ident: 10.1016/j.imbio.2011.01.006_bib0100 article-title: DNA methylation status of IL-8 gene promoter in oral cells of smokers and nonsmokers with chronic periodontitis publication-title: J. Clin. Periodontol. doi: 10.1111/j.1600-051X.2009.01446.x – volume: 89 start-page: 133 issue: 2 year: 2010 ident: 10.1016/j.imbio.2011.01.006_bib0130 article-title: Alteration of PTGS2 promoter methylation in chronic periodontitis publication-title: J. Dent. Res. doi: 10.1177/0022034509356512 – volume: 38 start-page: 210 year: 2003 ident: 10.1016/j.imbio.2011.01.006_bib0045 article-title: Patterns of chemokine receptors expression in different forms of human periodontal disease publication-title: J. Periodontol. Res. doi: 10.1034/j.1600-0765.2003.02012.x – volume: 165 start-page: 3626 issue: 7 year: 2000 ident: 10.1016/j.imbio.2011.01.006_bib0115 article-title: IL-10 but not IL-4, suppresses infection-stimulated bone resorption in vivo publication-title: J. Immunol. doi: 10.4049/jimmunol.165.7.3626 – volume: 78 start-page: 1339 year: 2005 ident: 10.1016/j.imbio.2011.01.006_bib0035 article-title: Different signaling pathways inhibit DNA methylation activity and up-regulated IFN-γ in human lymphocytes publication-title: J. Leukoc. Biol. doi: 10.1189/jlb.1004604 |
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Snippet | DNA methylation is characterized by the addition of methyl groups in cytosines within CpG islands. Unmethylated CpGs are related to transcriptionally active... Abstract DNA methylation is characterized by the addition of methyl groups in cytosines within CpG islands. Unmethylated CpGs are related to transcriptionally... |
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SubjectTerms | Advanced Basic Science Allergy and Immunology Base Sequence Case-Control Studies Chromatin - genetics Chromatin - immunology Chromatin - metabolism Chronic Periodontitis - genetics Chronic Periodontitis - immunology Chronic Periodontitis - metabolism CpG Islands - immunology Cytokines Cytosine - metabolism DNA Methylation - immunology Humans Inflammation Interferon-gamma - genetics Interferon-gamma - metabolism Interleukin-10 - genetics Interleukin-10 - metabolism Methylation Molecular Sequence Data Periodontitis Polymerase Chain Reaction Promoter Regions, Genetic - immunology Sequence Analysis, DNA Transcription, Genetic - genetics Transcription, Genetic - immunology |
Title | Methylation pattern of IFN-γ and IL-10 genes in periodontal tissues |
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