Ohta Shinsuke, Uemura Hiroji, Matsui Yoshiro, Ishiguro Hitoshi, Fujinami Kiyoshi, Kondo Keiichi, Miyamoto Hiroshi, Yazawa Takuya, Danenberg Kathleen, Danenberg Peter V, Tohnai Iwai, Kubota Yoshinobu
Department of Oral and Maxillofacial Surgery, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009 Jan;107(1):81-91. doi: 10.1016/j.tripleo.2008.08.027.
The p16 gene encodes a 16-kDa cyclin kinase inhibitor, and the p14ARF gene a 14-kDa protein, which acts as a cell cycle regulator or tumor suppressor in human cancer cells. Both genes are mapped on chromosome 9p21. Previous studies have suggested that the p16 gene has important roles in head and neck squamous cell carcinoma. To clarify carcinogenesis in oral squamous cell carcinoma (OSCC), we examined 44 primary OSCCs for alterations of p16 and p14ARF mRNA expression, the methylation status of the p16 gene promoter, the loss of heterozygosity (LOH) at the 9p21 locus, and p16 and p14ARF gene mutations. Alterations of p16 and p14ARF mRNA expression were seen in 27 (61.4%) of 44 and 10 (22.7%) of 44 of OSCC samples, respectively. Methylation of the p16 gene promoter region was detected in 28 (63.6%) of 44 samples, and LOH at 9p21 locus was found in 30 (68.2%) of 44. p16 and p14ARF gene mutations were observed in 4 (9.0%) of 44 and 2 (4.5%) of 44 samples, respectively. Suspected homozygous deletion (HD) was seen in 9 (20.5%) of 44. All cases except one (97.7%) showed alterations in p16, p14ARF, and their locus. These data indicate that the status of p16 and p14ARF genes in OSCC is frequently influenced by methylation, gene mutation, and allelic deletions. Furthermore, these genes and their 9p21 locus have various roles in the pathogenesis of OSCC.
p16基因编码一种16千道尔顿的细胞周期蛋白激酶抑制剂,p14ARF基因编码一种14千道尔顿的蛋白质,该蛋白质在人类癌细胞中作为细胞周期调节因子或肿瘤抑制因子发挥作用。这两个基因都定位于9号染色体的p21区域。先前的研究表明,p16基因在头颈部鳞状细胞癌中起重要作用。为了阐明口腔鳞状细胞癌(OSCC)的致癌机制,我们检测了44例原发性OSCC中p16和p14ARF mRNA表达的改变、p16基因启动子的甲基化状态、9p21位点的杂合性缺失(LOH)以及p16和p14ARF基因突变。在44例OSCC样本中,分别有27例(61.4%)和10例(22.7%)出现了p16和p14ARF mRNA表达的改变。在44例样本中的28例(63.6%)检测到p16基因启动子区域的甲基化,在44例中的30例(68.2%)发现9p21位点的LOH。分别在44例样本中的4例(9.0%)和2例(4.5%)观察到p16和p14ARF基因突变。在44例中的9例(20.5%)发现疑似纯合缺失(HD)。除1例(97.7%)外,所有病例均显示p16、p14ARF及其位点存在改变。这些数据表明,OSCC中p16和p14ARF基因的状态经常受到甲基化、基因突变和等位基因缺失的影响。此外,这些基因及其9p21位点在OSCC的发病机制中具有多种作用。