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Updated: Jan 27, 2026

Author Spotlight: Unlocking the Mysteries of Oral Potential Malignancies
Published on: August 11, 2023
Matrix metalloproteinases-3 gene-promoter polymorphism as a risk factor in oral submucous fibrosis: A systematic
Dipak D Ghatage1, Akshay A Dhobley1, Devendra H Palve1
1Oral Pathology and Microbiology Department, Government Dental College And Hospital, Nagpur, Maharashtra, India.
Abstract:
Oral submucous fibrosis (OSF) is a progressive potentially malignant disorder. Matrix metalloproteinase-3 (MMP3) regulates extracellular matrix remodelling, and promoter polymorphisms may influence OSF susceptibility. This systematic review and meta-analysis evaluated the association between MMP3 expression, promoter polymorphism, and OSF risk. Electronic databases (PubMed, Cochrane, Google Scholar, ScienceDirect) were searched for studies published between 2000 and 2023, assessing MMP3 expression or promoter polymorphism in OSF. Four eligible studies were analysed using RevMan 5.4. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated. Heterogeneity was assessed using I² statistics, and publication bias using funnel plot asymmetry and Egger's test. No significant association was observed between OSF risk and the homozygous 5A/5A genotype (OR = 2.34, 95% CI 0.63-8.71, P = 0.21, I² = 0%) or homozygous 6A/6A genotype (OR = 1.23, 95% CI 0.20-7.56, P = 0.83, I² = 89%). The heterozygous 5A/6A genotype showed a significant association with increased OSF susceptibility (OR = 2.75, 95% CI 1.63-4.64, P = 0.0002, I² = 0%). Egger's test indicated no publication bias. All studies demonstrated acceptable methodological quality. The MMP3 -1171 5A/6A promoter polymorphism is significantly associated with nearly three-fold increased OSF risk, whereas homozygous genotypes show no significant association. These findings suggest a role of MMP3 promoter variation in OSF pathogenesis. Larger, well-designed studies are required to validate these results and assess their diagnostic and preventive value.
Insights
The MMP3 -1171 5A/6A promoter polymorphism significantly increases oral submucous fibrosis risk by nearly threefold. Homozygous genotypes showed no significant association with this potentially malignant disorder.
Area of Science:
- Genetics
- Oncology
- Biochemistry
Background:
- Oral submucous fibrosis (OSF) is a progressive, potentially malignant oral disorder.
- Matrix metalloproteinase-3 (MMP3) plays a role in extracellular matrix remodeling.
- Genetic variations in MMP3 may influence susceptibility to OSF.
Purpose of the Study:
- To systematically review and meta-analyze the association between MMP3 expression, promoter polymorphism, and OSF risk.
- To evaluate the impact of MMP3 gene variations on OSF susceptibility.
Main Methods:
- Systematic literature search of PubMed, Cochrane, Google Scholar, and ScienceDirect (2000-2023).
- Meta-analysis of four eligible studies using RevMan 5.4, calculating pooled odds ratios (ORs) and 95% confidence intervals (CIs).
- Assessment of heterogeneity (I² statistics) and publication bias (funnel plot, Egger's test).
Main Results:
- The heterozygous MMP3 -1171 5A/6A promoter polymorphism was significantly associated with increased OSF susceptibility (OR = 2.75, 95% CI 1.63-4.64, P = 0.0002).
- No significant association was found for homozygous 5A/5A (OR = 2.34) or 6A/6A (OR = 1.23) genotypes.
- Egger's test indicated no publication bias; studies showed acceptable quality.
Conclusions:
- The MMP3 -1171 5A/6A promoter polymorphism is linked to a nearly threefold increased risk of OSF.
- MMP3 promoter variations may contribute to OSF pathogenesis.
- Further large-scale studies are needed to confirm these findings and explore diagnostic/preventive potential.
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