hpv相关鼻窦癌

Rina Jiromaru, Hidetaka Yamamoto, R. Yasumatsu, Takahiro Hongo, Yui Nozaki, K. Hashimoto, K. Taguchi, M. Masuda, T. Nakagawa, Y. Oda
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引用次数: 9

摘要

补充数字内容可在文本中找到。鼻鼻窦鳞状细胞癌(SNSCC)中人乳头瘤病毒(HPV)感染和表皮生长因子受体(EGFR)改变的患病率和预后价值尚不清楚。在SNSCC中,p16过表达作为HPV感染替代物的可靠性也尚不清楚。我们研究了HPV感染、EGFR改变和p16表达在SNSCC中的预后和诊断意义。我们通过HPV- rna原位杂交和EGFR基因拷贝数增加(CNG)显色原位杂交以及免疫组化检测p16、Rb和EGFR的蛋白表达来分析101例SNSCC的高危HPV感染。HPV感染(n=9, 8.9%)和p16过表达(n=15, 14.9%)与较好的总生存率相关(P分别为0.0042和0.005)。HPV+病例主要位于鼻腔,组织学无角化,Rb部分缺失。值得注意的是,40%(6/15)的p16+ SNSCCs为HPV−。其中2例免疫组化显示Rb表达完全缺失,提示上述差异的原因。EGFR CNG在30.5%的SNSCCs中检测到,与EGFR蛋白过表达相关(P=0.0001)。HPV感染与EGFR CNG是互斥的。HPV+/EGFR CNG -组的总生存率明显高于HPV - /EGFR CNG -组和HPV - /EGFR CNG+组(P分别为0.0471和0.0343)。我们的结果表明,HPV感染是SNSCC的一个有利的预后标记,但p16不是一个完美的替代标记;Rb表达谱可提高诊断准确性。基于HPV感染和EGFR拷贝数状态的SNSCCs分子亚分类可能为治疗策略提供重要信息。
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HPV-related Sinonasal Carcinoma
Supplemental Digital Content is available in the text. The prevalence and prognostic value of human papillomavirus (HPV) infection and epidermal growth factor receptor (EGFR) alteration in sinonasal squamous cell carcinoma (SNSCC) are not known. The reliability of p16 overexpression as a surrogate for HPV infection in SNSCC is also unclear. We investigated the prognostic and diagnostic significances of HPV infection, EGFR alteration, and p16 expression in SNSCC. We analyzed high-risk HPV infection by HPV-RNA in situ hybridization and EGFR gene copy number gain (CNG) by chromogenic in situ hybridization and by determining the protein expressions of p16, Rb, and EGFR by immunohistochemistry in 101 SNSCC cases. HPV infection (n=9, 8.9%) and p16 overexpression (n=15, 14.9%) were associated with better overall survival (P=0.0042 and 0.005, respectively). The HPV+ cases were located predominantly at the nasal cavity with nonkeratinizing histology and partial loss of Rb. Notably, 40% (6/15) of p16+ SNSCCs were HPV−. Two of these cases showed complete loss of Rb expression by immunohistochemistry, suggesting a reason for the above discrepancy. EGFR CNG, detected in 30.5% of the SNSCCs, was correlated with EGFR protein overexpression (P=0.0001). HPV infection and EGFR CNG were mutually exclusive. The HPV+/EGFR CNG− group had significantly better overall survival than the HPV−/EGFR CNG− and HPV−/EGFR CNG+ groups (P=0.0471 and 0.0343, respectively). Our results suggest that HPV infection is a favorable prognostic marker in SNSCC, but p16 is not a perfect surrogate marker; the Rb expression pattern may improve the diagnostic accuracy. The molecular subclassification of SNSCCs based on HPV infection and EGFR copy number status might provide important information for therapeutic strategies.
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