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Expression Analysis of Wnt Signaling Pathway Related Lncrnas in Periodontitis: A Pilot Case-Control Study Publisher



Ghafourifard S1 ; Dashti S2 ; Gholami L3 ; Badrlou E1, 4 ; Sadeghpour S1, 5 ; Hussen BM6 ; Hidayat HJ7 ; Nazer N8 ; Shadnoush M9 ; Sayad A1, 10, 11 ; Arefian N1
Authors
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Authors Affiliations
  1. 1. Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  2. 2. Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran
  3. 3. Department of Periodontics, Dental Research Center, Hamadan University of Medical Sciences, Hamadan, Iran
  4. 4. Pediatric Cell Therapy Research Center, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Hematopoietic Stem Cell Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  6. 6. Department of Pharmacognosy, College of Pharmacy, Hawler Medical University, Kurdistan Region, Erbil, Iraq
  7. 7. Department of Biology, College of Education, Salahaddin University-Erbil, Kurdistan Region, Erbil, Iraq
  8. 8. Department of Electrical Engineering, Sharif University of Technology, Tehran, Iran
  9. 9. Department of Clinical Nutrition, Faculty of Nutrition and Food Technology, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  10. 10. Dental Research Center, Research Institute for Dental Sciences, Dental School, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  11. 11. Pediatric Cell and Gene Therapy Research Center, Gene, Cell & Tissue Research Institute, Tehran University of Medical Sciences, Tehran, Iran

Source: Human Gene Published:2022


Abstract

LncRNAs are involved in the modulation of several signaling pathways which have a crucial effect in the differentiation of periodontal ligament cells and the induction of cementum regeneration. Autophagy and Wnt signaling are two important pathways with a wide range of interrelationships associated with periodontitis. We chose four lncRNAs based on their potential interaction with these two pathways. We examined the expression of FOXD2-AS1, NNT-AS1, GAS8-AS1, and CCAT1 lncRNAs in tissues and blood specimens of patients with periodontitis and unaffected controls using qRT-PCR. Expression amounts of FOXD2-AS1 were lower in blood of cases compared with controls (relative expression (RE) = 0.08, P value<0.001). Tissue expression of FOXD2-AS1 was similar between cases and controls. Difference in blood levels of FOXD2-AS1 was significant among female subjects (RE = 0.07, P-value = 0.01), but not among male subjects. In addition, we reported lower levels of NNT-AS1 in blood samples of cases versus controls (RE = 0.25, P value = 0.05). But such a pattern was not seen in tissue samples. Expression of GAS8-AS1 was lower in both tissue and blood specimens of patients compared with control (RE = 0.49, P value = 0.02 and RE = 0.32, P value = 0.03 for tissue and blood specimens, respectively). Moreover, the differences in blood expression of GAS8-AS1 were significant in female patients compared with female controls (RE = 0.25, P-value = 0.04). Expression of CCAT1 was significantly lower in both gingival tissue and blood samples of patients compared with control (RE for tissue samples = 0.36, P-value = 0.02 and RE for blood samples = 0.33, P-value = 0.02). This pattern of expression was also detected in tissue specimens obtained from male persons (RE = 0.23, P value = 0.02) and blood samples acquired from female patients compared with corresponding control samples (RE = 0.21, P value<0.001). FOXD2-AS1 showed the best AUC values for distinguishing periodontitis in blood samples (AUC = 0.78). Combination of transcript levels of all four lncRNAs increased the diagnostic power to 0.81 and 0.74 in the gingival tissues and blood specimens, respectively. Our study demonstrates dysregulation of several lncRNAs in the periodontitis. These transcripts might partake in the pathogenesis of periodontitis and could have a possible correlation with autophagy and Wnt signaling pathways. © 2022