Quintanilla-Martinez L, Kremer M, Keller G, Nathrath M, Gamboa-Dominguez A, Meneses A, Luna-Contreras L, Cabras A, Hoefler H, Mohar A, Fend F
Institute of Pathology, GSF-National Research Center for Environment and Health, Neuherberg, Germany.
Am J Pathol. 2001 Dec;159(6):2095-105. doi: 10.1016/S0002-9440(10)63061-1.
Nasal NK/T-cell lymphoma is a unique form of lymphoma highly associated with Epstein-Barr virus, and with a characteristic geographic distribution. Recently, we showed that p53 is overexpressed in a high percentage of nasal NK/T-cell lymphomas. The aim of this study was to analyze the status of the p53 gene, and correlate it with the expression of p53 protein and its downstream target, the cyclin-dependent kinase inhibitor p21, in a series of 25 cases of well-characterized nasal NK/T-cell lymphoma from Mexico. The highly conserved exons 5 to 8 of the p53 gene were amplified by polymerase chain reaction and screened for mutations by denaturing high-pressure liquid chromatography. Abnormal polymerase chain reaction products detected by denaturing high-pressure liquid chromatography and additional selected cases were sequenced. In addition, the incidence of loss of heterozygosity at the p53 locus was analyzed in 12 cases. Of the 25 patients, 17 were male and 8 female (M:F ratio, 2.1:1), with a median age of 43 years (range, 21 to 93 years). Morphologically, most of the cases were composed of a mixture of medium-sized cells and large transformed cells (21 cases), and four cases were composed exclusively of large transformed cells. Three different groups determined by p53 gene status and expression of p53 protein were identified: group 1 was p53 +/p53 mutated (five cases, all with p53 missense mutations). Morphologically, three of the five cases were composed of large cells. All five cases revealed overexpression of p53 in the majority of the tumor cells with a mean of 86%. Unexpectedly, three of these cases also showed overexpression of p21. Four of the five patients presented with clinical stage IVB and died with disease. Group 2 was p53+/p53 wild-type (10 cases). Histologically, nine cases were of the mixed type, and one of the large cell type. The percentage of p53 overexpressing cells was lower than in the previous group with a mean of 23%. p21 was positive in 7 of the 10 cases. Six patients in this group presented with clinical stages I to II and four patients with advanced disease (stage III and IV). Five patients are alive 12 to 120 months later (mean, 24 months), three with no evidence of disease. Group 3 was p53-/p53 wild-type (10 cases). All cases showed mixed cell morphology. p21 was positive in 5 of 10 cases. Four patients presented with clinical stage I to II and six patients with advanced disease. Four patients are alive with no evidence of disease 9 to 60 months later (mean, 10 months). Overall, p53 mutations were present in 24% (5 of 21) of the evaluable cases, all of them overexpressing p53 in the majority of tumor cells. Cases with p53 mutations were associated with large cell morphology (P = 0.0162) and presented more often with advanced stage disease. Loss of heterozygosity at chromosome 17p was found only in 2 of the 12 (17%) cases investigated, both cases showed p53 mutations of the remaining allele. P21 overexpression (60% of cases) is frequent in nasal NK/T-cell lymphoma and seems to be independent of p53 gene status. The overexpression of p53 and p21, independent of p53 mutations, although as yet not clear, might be the result of Epstein-Barr virus infection, and warrants further investigation.
鼻型NK/T细胞淋巴瘤是一种与EB病毒高度相关的独特淋巴瘤形式,具有特征性的地理分布。最近,我们发现p53在高比例的鼻型NK/T细胞淋巴瘤中过表达。本研究的目的是分析25例来自墨西哥的特征明确的鼻型NK/T细胞淋巴瘤中p53基因的状态,并将其与p53蛋白及其下游靶点细胞周期蛋白依赖性激酶抑制剂p21的表达相关联。通过聚合酶链反应扩增p53基因高度保守的外显子5至8,并通过变性高压液相色谱筛选突变。对变性高压液相色谱检测到的异常聚合酶链反应产物及其他选定病例进行测序。此外,分析了12例病例中p53基因座杂合性缺失的发生率。25例患者中,男性17例,女性8例(男:女比例为2.1:1),中位年龄43岁(范围21至93岁)。形态学上,大多数病例由中等大小细胞和大的转化细胞混合组成(21例),4例仅由大的转化细胞组成。根据p53基因状态和p53蛋白表达确定了三个不同的组:第1组为p53 +/p53突变型(5例,均为p53错义突变)。形态学上,5例中的3例由大细胞组成。所有5例在大多数肿瘤细胞中均显示p53过表达,平均为86%。出乎意料的是,其中3例还显示p21过表达。5例患者中有4例表现为临床IVB期并死于疾病。第2组为p53 +/p53野生型(10例)。组织学上,9例为混合型,1例为大细胞型。p53过表达细胞的百分比低于前一组,平均为23%。10例中有7例p21呈阳性。该组6例患者表现为临床I至II期,4例为晚期疾病(III和IV期)。5例患者在12至120个月后存活(平均24个月),3例无疾病证据。第3组为p53 -/p53野生型(10例)。所有病例均显示混合细胞形态。10例中有5例p21呈阳性。4例患者表现为临床I至II期,6例为晚期疾病。4例患者在9至60个月后存活且无疾病证据(平均10个月)。总体而言,可评估病例中有24%(21例中的5例)存在p53突变,所有这些病例在大多数肿瘤细胞中均过表达p53。p53突变的病例与大细胞形态相关(P = 0.0162),且更常表现为晚期疾病。在12例(17%)研究病例中仅2例发现17号染色体短臂杂合性缺失,这2例均显示其余等位基因的p53突变。p21过表达(60%的病例)在鼻型NK/T细胞淋巴瘤中很常见,似乎与p53基因状态无关。p53和p21的过表达,独立于p53突变,尽管目前尚不清楚,可能是EB病毒感染的结果,值得进一步研究。