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人乳头瘤病毒 DNA、E6*I-mRNA 表达和头颈部癌症的 p16INK4A 免疫组化——p16INK4A 作为替代标志物的有效性如何?

HPV DNA, E6*I-mRNA expression and p16INK4A immunohistochemistry in head and neck cancer - how valid is p16INK4A as surrogate marker?

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, Christian-Albrechts-University Kiel, Arnold-Heller-Straße 3, House 27, 24105 Kiel, Germany.

Department of Radiation Oncology, University Medical Center Hamburg-Eppendorf, D-Martinistr. 52, 20246 Hamburg, Germany.

出版信息

Cancer Lett. 2012 Oct 1;323(1):88-96. doi: 10.1016/j.canlet.2012.03.033. Epub 2012 Apr 3.

Abstract

It has been proposed that p16(INK4A) qualifies as a surrogate marker for viral oncogene activity in head and neck cancer (HNSCC). By analyzing 78 HNSCC we sought to validate the accuracy of p16(INK4A) as a reliable marker of active HPV infections in HNSCC. To this end we determined HPV DNA (HPVD) and E6*I mRNA (HPVR) expression status and correlated these results with p16(INK4A) staining. In tonsillar SCC 12/20 were HPVD+ and 12/12 of these showed active HPV infections whereas in non-tonsillar SCC 10/58 were HPVD+ and 5/10 showed active HPV infections. Thus, we prove about 8% of non-tonsillar SCC to be also correlated with HPV-associated carcinogenesis. Strikingly, 3/14 (21.4%) of tonsillar and non-tonsillar HPVD+/HPVR+ cases did not show p16(INK4A) overexpression and these cases would have been missed when applying initial p16(INK4A) staining only. However, in 13 cases negative for HPV, DNA p16(INK4A) was overexpressed. In conclusion, our data confirm tonsillar SCC to be predominantly but not only associated with active HPV infections. Furthermore, our data show that p16(INK4A) overexpression is not evident in a subgroup of HNSCC with active HPV infection. Definitive HPV data should therefore be utilized in diagnostics and treatment modalities of HPV positive and HPV negative HNSCC patients, resulting in a paradigm shift regarding these obviously different tumor entities.

摘要

已有研究提出,p16(INK4A) 可作为头颈部鳞癌(HNSCC)中病毒癌基因活性的替代标志物。通过分析 78 例 HNSCC,我们试图验证 p16(INK4A) 作为 HNSCC 中 HPV 感染活性的可靠标志物的准确性。为此,我们确定了 HPV DNA(HPVD)和 E6*I mRNA(HPVR)的表达状态,并将这些结果与 p16(INK4A) 染色相关联。在扁桃体鳞癌中,20 例中的 12 例为 HPVD+,这 12 例均显示出 HPV 感染的活性;而非扁桃体鳞癌中,58 例中的 10 例为 HPVD+,其中 5 例显示出 HPV 感染的活性。因此,我们证明了大约 8%的非扁桃体鳞癌也与 HPV 相关的致癌作用有关。值得注意的是,在扁桃体和非扁桃体的 HPVD+/HPVR+病例中,有 3/14(21.4%)例没有显示出 p16(INK4A) 的过表达,如果仅应用初始 p16(INK4A) 染色,这些病例将被遗漏。然而,在 13 例 HPV 阴性的病例中,p16(INK4A) 基因的 DNA 过表达。总之,我们的数据证实了扁桃体鳞癌主要与 HPV 感染的活性相关,但并非仅与 HPV 感染的活性相关。此外,我们的数据表明,在 HPV 感染活性的亚组 HNSCC 中,p16(INK4A) 的过表达并不明显。因此,在 HPV 阳性和 HPV 阴性 HNSCC 患者的诊断和治疗方案中,应使用明确的 HPV 数据,从而在这些明显不同的肿瘤实体方面实现范式转变。

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