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Impact of MDM2 single nucleotide polymorphism on oral squamous cell carcinoma risk
Jian-Li Xie1, Jing-Lei Yang, De-Sheng Liu
1School of Stomatology, Shandong University, Wenhuaxi Road, Jinan, 250012, Shandong, China.
Abstract:
Mouse Double Minute 2 (MDM2) has emerged as a pivotal cellular antagonist of p53 by destructing the suppressive function of p53 against tumorigenesis. The MDM2 309 T > G polymorphism has been studied for its association with oral squamous cell carcinoma (OSCC) susceptibility, but the evidence was confusing and inconclusive. Here, we performed a meta-analysis to estimate the effects of the 309 T > G polymorphism on the development of OSCC. The relevant studies were searched on both PubMed and Embase. We estimated the risk of OSCC using odds ratio (OR) and 95 % confidence interval (CI). In addition, between-study heterogeneity was measured by the χ (2)-based statistic test; sensitivity analysis, and the funnel plots and Egger's test were also performed in this meta-analysis. Based on five case-control studies with a total of 1,369 OSCC cases and 2,167 control subjects, the meta-analysis result showed neither increased nor decreased risk of OSCC associated with any genetic model of the 309 T > G polymorphism. Similar results were observed in the subgroup of Asians. No significant heterogeneity and publication bias were detected in the meta-analysis. The evidence provided in our study indicated that the 309 T > G polymorphism might have no significant contribution to susceptibility toward OSCC.
Insights
The Mouse Double Minute 2 (MDM2) 309 T>G polymorphism does not significantly affect oral squamous cell carcinoma (OSCC) risk. This meta-analysis found no increased or decreased susceptibility to OSCC associated with this genetic variation.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Mouse Double Minute 2 (MDM2) is a key regulator of p53, a tumor suppressor.
- The MDM2 309 T>G polymorphism's role in oral squamous cell carcinoma (OSCC) susceptibility is unclear.
- Previous studies on this association yielded conflicting results.
Purpose of the Study:
- To conduct a meta-analysis evaluating the association between the MDM2 309 T>G polymorphism and OSCC susceptibility.
- To clarify the conflicting evidence regarding this genetic polymorphism and cancer risk.
Main Methods:
- A systematic literature search was performed on PubMed and Embase.
- Five case-control studies involving 1,369 OSCC cases and 2,167 controls were included.
- Statistical analysis used odds ratios (OR) with 95% confidence intervals (CI), heterogeneity tests, sensitivity analysis, and publication bias assessment.
Main Results:
- The meta-analysis revealed no significant association between the MDM2 309 T>G polymorphism and OSCC risk across all genetic models.
- Subgroup analysis in Asian populations also showed no significant risk.
- No substantial heterogeneity or publication bias was detected.
Conclusions:
- The MDM2 309 T>G polymorphism does not appear to significantly contribute to OSCC susceptibility.
- Further research may be warranted, but current evidence suggests a lack of association.
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