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Characteristics of Head and Neck Squamous Cell Carcinoma Cell Lines Reflect Human Tumor Biology Independent of Primary Etiologies and HPV Status

机译:头颈部鳞状细胞癌细胞系的特征反映了人类肿瘤生物学而与主要病因和HPV状态无关

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摘要

Explanations for the differences in clinical outcomes in head and neck squamous cell carcinomas (HNSCCs) when compared by similar tumor location, stage, nodal status, human papillomavirus (HPV) status, and patient history remain elusive. Cell lines are an excellent tool of study for understanding the properties of cancers. However, HNSCC cell lines from progression-free and/or HPV-positive tumors are very rare. Here we studied HPV-positive and HPV-negative University of Michigan squamous cell carcinoma cell lines (2 HPV−, 2 HPV16+, 1 HPV18+) coming from donors with nonoropharyngeal sites and variant clinical outcomes. Cell morphology and proliferation were assessed, and immunofluorescence and Western blotting evaluated tumor biomarkers (TP53, RB1, p16, HPV E6 and E7, EGFR, Cyclin D1, Ki-67, and beta-catenin). Slow proliferation, long lag phase before exponential proliferation, lower maximal cell density, and higher wild-type TP53 expression were common to cell lines from patients who experienced long-term disease-free survival. In contrast, shorter lag phases, rapid proliferation, and high maximal cell density were observed in cell lines from patients who experienced aggressive tumor progression leading to death. Membrane-bound beta-catenin was present in all cell lines, but nuclear beta-catenin was associated with the more lethal cancers. In summary, the HNSCC cell lines present key characteristics, independent of primary etiologies and HPV infection, that mirror the behavior of the tumors from which they were derived.
机译:当通过相似的肿瘤位置,分期,淋巴结状态,人乳头瘤病毒(HPV)状态和患者病史进行比较时,无法解释头颈鳞状细胞癌(HNSCC)临床结局的差异。细胞系是了解癌症特性的出色研究工具。然而,来自无进展和/或HPV阳性肿瘤的HNSCC细胞系非常罕见。在这里,我们研究了来自非口咽部位和临床预后不同的供者的HPV阳性和HPV阴性的密歇根大学鳞状细胞癌细胞系(2 HPV-,2 HPV16 +,1 HPV18 +)。评估细胞形态和增殖,并通过免疫荧光和蛋白质印迹评估肿瘤生物标志物(TP53,RB1,p16,HPV E6和E7,EGFR,Cyclin D1,Ki-67和β-catenin)。缓慢增殖,指数增殖前的长期滞后阶段,较低的最大细胞密度和较高的野生型TP53表达是经历长期无病生存的患者的细胞系常见的现象。相反,在经历侵袭性肿瘤进展导致死亡的患者的细胞系中观察到更短的延迟期,快速增殖和最高的最大细胞密度。膜结合的β-catenin存在于所有细胞系中,但核β-catenin与更致命的癌症有关。总而言之,HNSCC细胞系呈现出关键特征,而与主要病因和HPV感染无关,这反映了其来源肿瘤的行为。

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