Cell Cycle Regulatory CCND1 G870A Gene Polymorphism and Periodontitis-Induced Oral Cancer: A Risk Analysis

Author:

Khan Mahvish1,Khan Saif2,Mandal Raju K.3,Mahto Hari S.4,Lohani Mohtashim5,Ahmad Saheem6,Sherwani Subuhi7,Jandrajupalli Suresh B.8,Haque Shafiul3

Affiliation:

1. Department of Biology, College of Science ,, University of Ha’il , Ha’il-2440 , Saudi Arabia

2. Department of Basic Dental and Medical Sciences, College of Dentistry , Ha’il University , Ha’il-2440 , Saudi Arabia

3. Research and Scientific Studies Unit, College of Nursing & Allied Health Sciences , Jazan University , Jazan-45142 , Saudi Arabia

4. Centre for Life Sciences , Central University of Jharkhand , Ranchi-835205, Jharkhand , India

5. Department of Emergency Medical Services , College of Applied Medical Sciences, Jazan University , Jazan-45142 , Saudi Arabia

6. Department of Clinical Laboratory Sciences, College of Applied Medical Sciences , University of Ha’il , Ha’il-2440 , Saudi Arabia

7. Department of Biology, College of Science , University of Ha’il , Ha’il-2440 , Saudi Arabia

8. Department of Preventive Dentistry , College of Dentistry, University of Ha’il , Ha’il-2440 , Saudi Arabia

Abstract

Abstract Strong association has been recently observed between periodontitis/gingivitis and Oral squamous cell carcinoma (OSCC). A high incidence of oral cancer has been reported in the case of chronic periodontitis. Recently Cell cycle regulatory /Senescence genes have been associated with Gingivitis/ Periodontitis susceptibility. Cyclin D1 is one such cell cycle regulatory gene. Several findings have reported that Cyclin D1 (CCND1) G870A Single nucleotide polymorphism is associated with oral cancer (OC) risk, but yielded inconsistent data across different studies. This meta-analysis explores the precise relationship between CCND1 G870A polymorphism and OC risk. PubMed (Medline), EMBASE, & Google Scholar databases were searched for eligible studies and pooled odds ratios (ORs) and 95% confidence intervals (CI) were calculated. Newcastle-Ottawa analysis was done for selected articles quality assessment, bias in publication (if any) was estimated through Funnel plots and Egger’s test. Pooled analysis from eleven eligible studies suggests that CCND1 G870A polymorphism is not significantly associated with OC risk. Sub-group analysis by ethnicity failed to show any association. Sequential single study omission was performed to determine the credibility and resilience of the inferences drawn.

Publisher

Walter de Gruyter GmbH

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