Molecular signatures of chronic periodontitis in gingiva: A genomic and proteomic analysis

Guzeldemir-Akcakanat E., Alkan B., Sunnetci-Akkoyunlu D., Gürel B., Balta V. M., Kan B., ...Daha Fazla

JOURNAL OF PERIODONTOLOGY, cilt.90, sa.6, ss.663-673, 2019 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 90 Sayı: 6
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1002/jper.18-0477
  • Dergi Adı: JOURNAL OF PERIODONTOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.663-673
  • Anahtar Kelimeler: chronic periodontitis, enoyl-CoA hydratase, inflammation, genomics, gingiva, proteomics, proteogenomics, pERp1, GENE-EXPRESSION PROFILE, WIDE ASSOCIATION, TISSUE TRANSCRIPTOMES, MZB1, PATHOGENESIS, MICROARRAY, PROPOSAL
  • Kocaeli Üniversitesi Adresli: Evet

Özet

Background To elucidate molecular signatures of chronic periodontitis (CP) using gingival tissue samples through omics-based whole-genome transcriptomic and whole protein profiling. Methods Gingival tissues from 18 CP and 25 controls were analyzed using gene expression microarrays to identify gene expression patterns and the proteins isolated from these samples were subjected to comparative proteomic analysis by liquid chromatography-tandem mass spectrometry (LC-MS/MS). The data from transcriptomics and proteomics were integrated to reveal common shared genes and proteins. Results The most upregulated genes in CP compared with controls were found as MZB1, BMS1P20, IGLL1/IGLL5, TNFRSF17, ALDH1A1, KIAA0125, MMP7, PRL, MGC16025, ADAM11, and the most upregulated proteins in CP compared with controls were BPI, ITGAM, CAP37, PCM1, MMP-9, MZB1, UGTT1, PLG, RAB1B, HSP90B1. Functions of the identified genes were involved cell death/survival, DNA replication, recombination/repair, gene expression, organismal development, cell-to-cell signaling/interaction, cellular development, cellular growth/proliferation, cellular assembly/organization, cellular function/maintenance, cellular movement, B-cell development, and identified proteins were involved in protein folding, response to stress, single-organism catabolic process, regulation of peptidase activity, and negative regulation of cell death. The integration and validation analysis of the transcriptomics and proteomics data revealed two common shared genes and proteins, MZB1 and ECH1. Conclusion Integrative data from transcriptomics and proteomics revealed MZB1 as a potent candidate for chronic periodontitis.