Fracchiolla N S, Pruneri G, Pignataro L, Carboni N, Capaccio P, Boletini A, Buffa R, Neri A
Istituto di Scienze Mediche, Università di Milano, Ospedale Maggiore, I.R.C.C.S., Milan, Italy.
Cancer. 1997 Mar 15;79(6):1114-21.
The molecular pathogenesis of laryngeal squamous cell carcinomas (LSCCs) is still only partially understood, although genetic alterations affecting various protooncogenes or tumor suppressor genes have often been detected.
To improve their understanding of the role of cyclin D1 in the pathogenesis of LSCCs, the authors investigated the expression of cyclin D1 protein and the amplification status of the bcl-1/cyclin D1 locus in a panel of 58 pathologic samples.
Expression of cyclin D1 protein was detected in 23 of the 58 patients (approximately 39%), 14 of whom had lymph node metastases (approximately 61%); of the remaining 35 patients without any detectable cyclin D1 expression, 7 had lymph node metastases (20%). Expression of cyclin D1 was detectable in 5% of the specimens of normal mucosa, 13% of those with mild-to-moderate dysplasia, and 25% of those with severe dysplasia. Amplification of the bcl-1/cyclin D1 locus was detected in 12 of the 49 LSCCs investigated (approximately 24%), 7 of which had lymph node metastases (approximately 58%); of the remaining 37 LSCCs with an apparently normal copy number of the cyclin D1 locus, 12 had lymph node metastases (approximately 32%). The authors found almost complete concordance between locus amplification and protein expression. Statistical analysis showed a correlation between cyclin D1 expression and both the presence of lymph node metastases (P < 0.01) and advanced clinical stage (P < 0.02).
The authors' observations suggest that the deregulation of cyclin D1 expression may be involved in the pathogenesis of more aggressive LSCCs.
尽管经常检测到影响各种原癌基因或肿瘤抑制基因的基因改变,但喉鳞状细胞癌(LSCC)的分子发病机制仍仅部分为人所知。
为了更好地理解细胞周期蛋白D1在LSCC发病机制中的作用,作者研究了58例病理样本中细胞周期蛋白D1蛋白的表达以及bcl-1/细胞周期蛋白D1基因座的扩增状态。
58例患者中有23例检测到细胞周期蛋白D1蛋白表达(约39%),其中14例有淋巴结转移(约61%);其余35例未检测到细胞周期蛋白D1表达的患者中,7例有淋巴结转移(20%)。正常黏膜标本中5%可检测到细胞周期蛋白D1表达,轻度至中度发育异常标本中13%可检测到,重度发育异常标本中25%可检测到。在49例研究的LSCC中,12例检测到bcl-1/细胞周期蛋白D1基因座扩增(约24%),其中7例有淋巴结转移(约58%);其余37例细胞周期蛋白D1基因座拷贝数明显正常的LSCC中,12例有淋巴结转移(约32%)。作者发现基因座扩增与蛋白表达几乎完全一致。统计分析表明,细胞周期蛋白D1表达与淋巴结转移的存在(P < 0.01)和临床晚期(P < 0.02)均相关。
作者的观察结果表明,细胞周期蛋白D1表达失调可能参与了侵袭性更强的LSCC的发病机制。