Predictive value of CDKN2A/p16INK4a expression in the malignant transformation of oral potentially malignant disorders: Systematic review and meta-analysis

被引:6
作者
Lorenzo-Pouso, Alejandro I. [1 ,2 ]
Caponio, Vito Carlo Alberto [3 ]
Silva, Fabio Franca Vieira E. [1 ,2 ]
Perez-Jardon, Alba [1 ,2 ]
Alvarez-Calderon-Igesias, Oscar [4 ]
Gandara-Vila, Pilar [1 ,2 ,5 ]
Pannone, Giuseppe [3 ]
Perez-Sayans, Mario [1 ,2 ]
机构
[1] Univ Santiago De Compostela, Fac Med & Dent, Oral Med Oral Surg & Implantol Unit, MedOralRes Grp, La Coruna 15782, Spain
[2] Hlth Res Inst Santiago De Compostela IDIS, Santiago De Compostela 15706, Spain
[3] Univ Foggia, Dept Clin & Expt Med, I-71122 Foggia, Italy
[4] Univ A Coruna, Fac Nursing & Podiatry, Dept Hlth Sci, Res Hlth & Podiatry Grp, La Coruna 15008, Spain
[5] Univ Santiago De Compostela, Fac Med & Dent, Oral Med Oral Surg & Implantol Unit, Rua Entrerios S-N, La Coruna 15782, Spain
关键词
p16INK4a Gene; OPMD; Meta-analysis; Prognosis; Immunohistochemistry; HIGH-RISK; CANCER; DYSPLASIA; BIOMARKER; LEUKOPLAKIA; BIAS;
D O I
10.1016/j.prp.2023.154656
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: Management of oral potentially malignant disorders (OPMDs) is still challenging. Despite the diagnostic ascertainment by bioptic examination, this method is poorly informative of the prognosis and subsequent malignant transformation. Prognosis is based on histological findings by grading of dysplasia. Immunohistochemical expression of p16INK4a has been investigated in different studies, with controversial results. In this scenario, we systematically revised the current evidence about p16INK4a immunohistochemical expression and the risk of malignization of OPMDs. Material and methods: After a proper set of keywords combination, 5 databases were accessed and screened to select eligible studies. The protocol was previously registered on PROSPERO (Protocol ID: CRD42022355931). Data were obtained directly from the primary studies as a measure to determine the relationship between CDKN2A/P16INK4a expression and the malignant transformation of OPMDs. Heterogeneity and publication bias were investigated by different tools, such as Cochran's Q test, Galbraith plot and Egger and Begg Mazumdar's rank tests. Results: Meta-analysis revealed a twofold increased risk to malignant development (RR = 2.01, 95% CI = 1.36-2.96 - I2 = 0%). Subgroup analysis did not highlight any relevant heterogeneity. Galbraith plot showed that no individual study could be considered as an important outlier. Conclusion: Pooled analysis showed that p16INK4a assessment may arise adjunct tool to dysplasia grading, leading to an optimized determination of the potential progression to cancer of OPMDs. The p16INK4a overexpression analysis by immunohistochemistry techniques has a multitude of virtues that may facilitate its incorporation in the day-to-day prognostic study of OPMDs.
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页数:9
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