Villuendas R, Sánchez-Beato M, Martínez J C, Saez A I, Martinez-Delgado B, García J F, Mateo M S, Sanchez-Verde L, Benítez J, Martínez P, Piris M A
Department of Genetics, Virgen de la Salud Hospital, Toledo, Spain.
Am J Pathol. 1998 Sep;153(3):887-97. doi: 10.1016/S0002-9440(10)65630-1.
The CDKN2A gene located on chromosome region 9p21 encodes the cyclin-dependent kinase-4 inhibitor p16/INK4A, a negative cell cycle regulator. We analyzed p16/INK4A expression in different types of non-Hodgkin's lymphoma to determine whether the absence of this protein is involved in lymphomagenesis, while also trying to characterize the genetic events underlying this p16/INK4A loss. To this end, we investigated the levels of p16/INK4A protein using immunohistochemical techniques in 153 cases of non-Hodgkin's lymphoma, using as reference the levels found in reactive lymphoid tissue. The existence of gene mutation, CpG island methylation, and allelic loss were investigated in a subset of 26 cases, using single-strand conformational polymorphism and direct sequencing, Southern Blot, polymerase chain reaction, and microsatellite analysis, respectively. Loss of p16/INK4A expression was detected in 41 of the 112 non-Hodgkin's lymphomas studied (37%), all of which corresponded to high-grade tumors. This loss of p16/INK4A was found more frequently in cases showing tumor progression from mucosa-associated lymphoid tissue low-grade lymphomas (31 of 37) or follicular lymphomas (4 of 4) into diffuse large B-cell lymphomas. Analysis of the status of the p16/INK4A gene showed different genetic alterations (methylation of the 5'-CpG island of the p16/INK4A gene, 6 of 23 cases; allelic loss at 9p21, 3 of 16 cases; and nonsense mutation, 1 of 26 cases). In all cases, these events were associated with loss of the p16/INK4A protein. No case that preserved protein expression contained any genetic change. Our results demonstrate that p16/INK4A loss of expression contributes to tumor progression in lymphomas. The most frequent genetic alterations found were 5'-CpG island methylation and allelic loss.
位于染色体区域9p21的CDKN2A基因编码细胞周期蛋白依赖性激酶4抑制剂p16/INK4A,它是一种负性细胞周期调节因子。我们分析了不同类型非霍奇金淋巴瘤中p16/INK4A的表达情况,以确定该蛋白缺失是否参与淋巴瘤的发生,同时试图明确导致这种p16/INK4A缺失的基因事件。为此,我们采用免疫组织化学技术,以反应性淋巴组织中的水平为参照,检测了153例非霍奇金淋巴瘤中p16/INK4A蛋白的水平。分别使用单链构象多态性和直接测序、Southern印迹、聚合酶链反应以及微卫星分析,对26例样本进行检测,以研究基因突变、CpG岛甲基化和等位基因缺失的情况。在112例研究的非霍奇金淋巴瘤中,有41例(37%)检测到p16/INK4A表达缺失,所有这些均为高级别肿瘤。在显示肿瘤从黏膜相关淋巴组织低级别淋巴瘤(37例中的31例)或滤泡性淋巴瘤(4例中的4例)进展为弥漫性大B细胞淋巴瘤的病例中,p16/INK4A缺失更为常见。对p16/INK4A基因状态的分析显示存在不同的基因改变(p16/INK4A基因5'-CpG岛甲基化,23例中的6例;9p21等位基因缺失,16例中的3例;以及无义突变,26例中的1例)。在所有病例中,这些事件均与p16/INK4A蛋白缺失相关。没有保留蛋白表达的病例存在任何基因改变。我们的结果表明,p16/INK4A表达缺失促进淋巴瘤的肿瘤进展。最常见的基因改变是5'-CpG岛甲基化和等位基因缺失。