Lulić Lucija, Jakovčević Antonia, Kovačić Iva, Manojlović Luka, Dediol Emil, Skelin Josipa, Tomaić Vjekoslav
Division of Molecular Medicine, Ruđer Bošković Institute, Bijenička 54, 10000 Zagreb, Croatia.
Clinical Department of Pathology and Cytology, University Hospital Center Zagreb, 10000 Zagreb, Croatia.
Pathogens. 2023 Aug 3;12(8):1013. doi: 10.3390/pathogens12081013.
Infection with human papillomaviruses (HPVs), in particular with HPV type 16, is now considered to be a key risk factor for the development of a subset of oropharyngeal squamous cell carcinomas (OPSCC) that show different epidemiological, clinical, and prognostic characteristics from HPV-negative (HPV-) OPSCCs. So far, extensive research efforts aiming to distinguish these two distinct entities have not identified specific biomarkers, nor led to different therapies. Previous research has shown that HPV16 E6 oncoprotein binds NHERF2, inducing its proteasomal degradation, and consequently increasing cell proliferation; we therefore aimed to investigate how this might be reflected in human histological samples. We analyzed NHERF2 expression patterns in HPV16-positive (HPV16+) and HPV- OPSCC samples, to investigate any potential differences in NHERF2 pattern. Interestingly, we observed a statistically significant decrease in NHERF2 levels in HPV16+ and poorly differentiated HPV- OPSCCs, compared with healthy tissue. Furthermore, we observed a significant reduction in the percentage of NHERF2 immunoreactive cancer cells in HPV16+ tumors, compared with well and moderately differentiated HPV- OPSCCs, suggesting the importance of 16E6's targeting of NHERF2 in HPV-driven oncogenesis in the head and neck area.
人乳头瘤病毒(HPV)感染,尤其是16型HPV感染,现在被认为是口咽鳞状细胞癌(OPSCC)的一个亚组发生发展的关键危险因素,该亚组与HPV阴性(HPV-)的OPSCC表现出不同的流行病学、临床和预后特征。到目前为止,旨在区分这两种不同实体的广泛研究工作尚未确定具体的生物标志物,也未导致不同的治疗方法。先前的研究表明,HPV16 E6癌蛋白与NHERF2结合,诱导其蛋白酶体降解,从而增加细胞增殖;因此,我们旨在研究这在人体组织学样本中可能如何体现。我们分析了HPV16阳性(HPV16+)和HPV-的OPSCC样本中NHERF2的表达模式,以研究NHERF2模式的任何潜在差异。有趣的是,与健康组织相比,我们观察到HPV16+和低分化HPV-的OPSCC中NHERF2水平有统计学意义的下降。此外,与高分化和中分化HPV-的OPSCC相比,我们观察到HPV16+肿瘤中NHERF2免疫反应性癌细胞的百分比显著降低,这表明16E6靶向NHERF2在HPV驱动的头颈部肿瘤发生中具有重要意义。