Evidence map›Paper›PMID 30334169›Full record

ArticleClinical oral investigations2019

Hedgehog signaling pathway and vitamin D receptor gene variants as potential risk factors in odontogenic cystic lesions.

Marko Magic, Katarina Zeljic, Stevo Jovandic, Jelena Stepic, Marko Pejovic, Snjezana Colic, Zvonko Magic, Gordana Supic

Abstract read
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In one paragraph

Article in Clinical oral investigations, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.3field-weighted citation impact, top 42% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Biology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. A systematic review on odontogenic cysts and tumours.Journal of oral and maxillofacial pathology : JOMFP
    Review
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Marko MagicDepartment of Oral Surgery, School of Dentistry, University of Belgrade, Belgrade, Serbia.
Katarina ZeljicFaculty of Biology, University of Belgrade, Belgrade, Serbia.
Stevo JovandicInstitute for Medical Research, Military Medical Academy, Belgrade, Serbia.
Jelena StepicDepartment of Oral Surgery, School of Dentistry, University of Belgrade, Belgrade, Serbia.
Marko PejovicDepartment of Oral Surgery, School of Dentistry, University of Belgrade, Belgrade, Serbia.
Snjezana ColicDepartment of Oral Surgery, School of Dentistry, University of Belgrade, Belgrade, Serbia.
Zvonko MagicInstitute for Medical Research, Military Medical Academy, Belgrade, Serbia.
Gordana SupicInstitute for Medical Research, Military Medical Academy, Belgrade, Serbia. gogasupic@orion.rs.ORCID http://orcid.org/0000-0003-0350-4733
University of Belgrade · RSMilitary Medical Academy · RS

Funding

Faculty of Medicine, Military Medical Academy, Belgrade, Serbia MFVMA/11/16-18
6 · The paper itself

Abstract

objectivesGenetic variants in the hedgehog signaling pathway and VDR gene are involved in inflammatory responses and neoplastic transformation. Current study investigated whether single-nucleotide polymorphisms in the hedgehog pathway genes PTCH1, GLI1, SMO, and VDR contribute to susceptibility to odontogenic cystic lesions, odontogenic keratocysts, or inflammatory radicular cysts. MATERIAL AND

methodsCurrent study examined polymorphisms of PTCH1 (rs357564) and PTCH1 insertion (IVS1-83), GLI1 (rs2228224, rs2228226), SMO (rs2228617), and VDR (rs2228570, rs731236, rs7975232). A case-control study was conducted on 41 keratocyst cases, 43 radicular cyst cases, and control group of 93 healthy individuals without cystic lesions, radiographically confirmed. Single-nucleotide polymorphisms were assessed by real-time and TaqMan SNP genotyping assays, while PTCH1 insertion 18 bp IVS1-83 polymorphism was determined by PCR.

resultsThe difference in genotype distribution between keratocyst cases and control group was observed for PTCH1 IVS1-83 and GLI1 rs2228224 polymorphism (p = 0.022, p = 0.030, respectively). Homozygous mutant GG genotype within GLI1 rs2228224 is associated with increased susceptibility for odontogenous keratocysts, with adjusted odds ratio of 4.098 (confidence interval of 1.482-11.328, p = 0.007).

conclusionGLI1 rs2228224 and PTCH1 polymorphisms could predispose to odontogenic keratocysts. CLINICAL RELEVANCE: Variants in hedgehog signaling pathway genes, such as GLI1 and PTCH1, and vitamin D receptor gene, might be considered as molecular risk factors in odontogenic cystic lesions and potential targets for novel therapeutic approaches.

Indexed as

Signal TransductionCase-Control StudiesHedgehog ProteinsHumansOdontogenic CystsPatched-1 ReceptorPolymorphism, Single NucleotideReceptors, CalcitriolRisk FactorsSmoothened ReceptorZinc Finger Protein GLI1GLI1 protein, humanHedgehog ProteinsPatched-1 ReceptorPTCH1 protein, humanReceptors, CalcitriolSmoothened ReceptorSMO protein, humanVDR protein, humanZinc Finger Protein GLI1GLI1Hedgehog signalingOdontogenic keratocystsPolymorphismPTCH1Vitamin D receptor

Identifiers

PMID30334169
OpenAlexW2897298843

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.