Kornfehl Johannes, Hager Gudrun, Gedlicka Claudia, Formanek Michael
Department of Oto-Rhino-Laryngology, Head and Neck Surgery, General Hospital, University of Vienna, Austria.
Acta Otolaryngol. 2002 Apr;122(3):338-42. doi: 10.1080/000164802753648277.
Epidemiologic studies have provided evidence of an alcohol-associated increased risk of upper aerodigestive tract cancers. Recently we reported ethanol-induced proliferation in a squamous cell carcinoma of the head and neck (SCCHN) cell line, but the underlying mechanisms are unknown. In order to further clarify these findings, major G0/G1-regulating proteins were investigated in the present study. Synchronized cells of a SCCHN line (JP-PA) and a human immortalized keratinocyte line (HaCaT)-used as a control-were cultured with or without 10(-3) M ethanol for up to 96 h. At distinct time intervals the expression of cyclin D1 and the inhibitors p16, p18, p19 and p21 were determined by Western blot analyses. In both lines ethanol had no influence on the protein expression of cyclin D1. In contrast, distinct downregulations of p21, p18 and p19 were detectable at the protein level. The p16 protein was not expressed in the SCCHN line and was unchanged in the control line after the addition of ethanol. In these in vitro experiments the marked downregulation of important cell-cycle inhibitors may accelerate progression from the G1 to the S phase of the cell cycle. The relevance of our findings to in vivo conditions remains speculative, but the observed mechanisms of significantly reduced expression of cell-cycle inhibitor proteins may be involved in the carcinogenesis of head and neck malignancies.
流行病学研究已提供证据表明,酒精会增加上呼吸消化道癌症的发病风险。最近我们报道了乙醇可诱导头颈部鳞状细胞癌(SCCHN)细胞系增殖,但潜在机制尚不清楚。为了进一步阐明这些发现,本研究对主要的G0/G1调节蛋白进行了研究。将SCCHN细胞系(JP-PA)的同步化细胞和作为对照的人永生化角质形成细胞系(HaCaT)在有或无10(-3) M乙醇的情况下培养长达96小时。在不同的时间间隔,通过蛋白质印迹分析确定细胞周期蛋白D1以及抑制剂p16、p18、p19和p21的表达。在这两种细胞系中,乙醇对细胞周期蛋白D1的蛋白质表达均无影响。相比之下,在蛋白质水平可检测到p21、p18和p19有明显下调。p16蛋白在SCCHN细胞系中未表达,在加入乙醇后对照细胞系中也未发生变化。在这些体外实验中,重要细胞周期抑制剂的明显下调可能会加速细胞周期从G1期进入S期。我们的发现与体内情况的相关性仍属推测,但观察到的细胞周期抑制剂蛋白表达显著降低的机制可能参与了头颈部恶性肿瘤的致癌过程。