缺乏CD44和Sox-2过表达是HPV阳性口咽癌患者的两个独立的有利预后因素。

Marta Kołodziej-Rzepa, Beata Biesaga, Anna Janecka-Widła, Anna Mucha-Małecka
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引用次数: 1

摘要

在我们早期的出版物中,在63例口咽癌患者中,我们在25例肿瘤(39.7%)中发现HPV16感染(通过qPCR评估),CD44、CD98、ALDH1/2和Nanog In的免疫组织化学过表达分别为43例(68.2%)、30例(47.6%)、33例(52.4%)和53例(84.1%)。通过分析CD44、CD98、ALDH1/2,我们还发现,HPV16阳性患者缺乏CD44过表达预示着良好的预后。本研究的目的是比较Nanog, Oct3/4, Sox-2表达与CD44, CD98, ALDH1/2免疫反应性(我们之前评估过)和临床病理特征在HPV16阳性和HPV16阴性患者亚组中的预后潜力。方法:采用免疫组化方法对63例口咽癌患者的Oct3/4和Sox-2的表达情况进行检测。在生存分析中,采用了两个终点:总生存期(OS)和无病生存期(DFS)。结果:Oct3/4和Sox-2过表达的患者分别为0例(0.0%)和27例(42.9%)。在HPV16阳性亚组中,Sox-2过表达缺失患者的DFS显著高于Sox-2过表达患者(p = 0.003)。在HPV16阴性亚组中,Nanog和Sox-2免疫表达对OS和DFS无显著影响。在HPV16阳性亚组的多变量分析中,缺乏CD44过表达(p = 0.012)和缺乏Sox-2过表达(p = 0.027)是阳性的独立预后因素。结论:基于CD44和Sox-2的免疫反应性,可以区分hpv16阳性口咽癌患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lack of CD44 and Sox-2 Overexpression as Two Independent Favourable Prognostic Factors in HPV Positive Patients with Oropharyngeal Cancers.

Introduction: In our earlier publications, in the group of 63 patients with oropharyngeal cancer, we have found HPV16 infection (assessed by qPCR) in 25 tumours (39.7%), immunohistochemical overexpression of CD44, CD98, ALDH1/2 and Nanog in, respectively: 43 (68.2%), 30 (47.6%), 33 (52.4%), and 53 (84.1%) cancers. Analysing CD44, CD98, ALDH1/2, we have also shown that lack of CD44 overexpression indicates excellent prognosis in patients with HPV16 positivity. The aim of the present study was to compare prognostic potential of Nanog, Oct3/4, Sox-2 expression in relation to CD44, CD98, ALDH1/2 immunoreactivity (assessed by us earlier) and clinicopathological features in the subgroups of patients: with HPV16 positivity and HPV16 negativity.

Methods: Status of Oct3/4 and Sox-2 expression was assessed for 63 patients with oropharyngeal cancers based on immunohistochemistry. In survival analysis, two endpoints were applied: overall survival (OS) and disease-free survival (DFS).

Results: Overexpression of Oct3/4 and Sox-2 was found in 0 (0.0%) and 27 (42.9%) of patients. In the subgroup with HPV16 positivity, the DFS for patients with lack of Sox-2 overexpression was significantly (p = 0.003) higher than for patients with Sox-2 overexpression. In the subgroup with HPV16 negativity, Nanog and Sox-2 immunoexpression did not significantly influence OS and DFS. In multivariate analysis performed for the subgroup with HPV16 positivity, lack of CD44 overexpression (p = 0.012) and lack of Sox-2 overexpression (p = 0.027) were positive independent prognostic factors.

Conclusion: Based on CD44 and Sox-2 immunoreactivity, it is possible to differentiate the prognosis of HPV16-positive patients with oropharyngeal cancers.

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