de Abreu Priscila Marinho, Sol Marcella, Bianchi Molini Patrícia Roccon, Daniel Camila Batista, Camisasca Danielle Resende, von Zeidler Sandra Ventorin
Biotechnology Program, Universidade Federal do Espírito Santo - UFES, Vitória, ES, Brazil.
Department of Pathology, Universidade Federal do Espírito Santo - UFES, Vitória, ES, Brazil.
J Oral Maxillofac Pathol. 2024 Apr-Jun;28(2):253-260. doi: 10.4103/jomfp.jomfp_195_23. Epub 2024 Jul 11.
The aim of the present study was to examine the immunoexpression of CD44, p16 and VEGF in oral squamous cell carcinoma (OSCC) and correlate them to clinicopathological parameters and survival outcomes in order to clarify their prognostic impact.
A total of 68 individuals with OSCC recruited between 2011 and 2015 from two referral centres were enrolled in the study. The samples were placed on silanized glass slides and subjected to immunohistochemistry using anti-p16, anti-CD44 and anti-VEGF antibodies. The H Score was used for p16 and VEGF, while CD44 was scored according to the percentage of stained cells. Chi-square tests and Fisher's exact probability tests were used to compare clinicopathological characteristics according to the immunohistochemical expression, while overall survival and disease-free survival were estimated and compared using the Kaplan-Meier method and log-rank test, respectively. For all hypothesis tests, the level of significance was set at ≤ 0.05.
No correlation was observed between the expression of tumour VEGF, p16 and CD44, and the clinicopathological characteristics analysed. Patients with high stromal VEGF expression had better disease-free survival than patients with low VEGF expression ( = 0.023).
In summary, P16, CD44 and tumour VEGF did not prove to be good prognostic biomarkers. Stromal VEGF expression is suggested to be a good candidate prognostic biomarker, although additional studies are needed.
本研究旨在检测口腔鳞状细胞癌(OSCC)中CD44、p16和VEGF的免疫表达,并将它们与临床病理参数及生存结果相关联,以阐明其预后影响。
2011年至2015年间从两个转诊中心招募的68例OSCC患者纳入本研究。将样本置于硅烷化载玻片上,使用抗p16、抗CD44和抗VEGF抗体进行免疫组织化学检测。p16和VEGF采用H评分,而CD44根据染色细胞百分比进行评分。采用卡方检验和Fisher精确概率检验根据免疫组化表达比较临床病理特征,同时分别采用Kaplan-Meier法和对数秩检验估计并比较总生存期和无病生存期。对于所有假设检验,显著性水平设定为≤0.05。
未观察到肿瘤VEGF、p16和CD44的表达与所分析的临床病理特征之间存在相关性。基质VEGF高表达的患者比VEGF低表达的患者无病生存期更好(P = 0.023)。
总之,P16、CD44和肿瘤VEGF未被证明是良好的预后生物标志物。尽管还需要进一步研究,但基质VEGF表达被认为是一个良好的潜在预后生物标志物。