Yamamoto Y, Kishimoto Y, Virmani A K, Smith A, Vuitch F, Albores-Saavedra J, Gazdar A F
Hamon Center for Therapeutic Oncology Research, University of Texas Southwestern Medical Center, Dallas 75235-8593, USA.
Hum Pathol. 1996 Aug;27(8):782-6. doi: 10.1016/s0046-8177(96)90449-9.
Pleomorphic adenoma (PA) is the most common benign tumor of salivary glands. Carcinomas in pleomorphic adenomas (CPAs) may arise by malignant transformation of the epithelial components of PAs. Occasionally, transitional zones containing cells with histological features intermediate between those of the benign PA and carcinomatous components of CPA are identified. After careful microdissection of archival microslides, the authors studied 12 cases of CPAs and their attendant adenomatous and transitional areas for mutations in the p53, RB, and K-ras genes, and at chromosomal loci 5q and 9p. The authors failed to find mutations in the K-ras gene or 9p locus. A relatively high rate of mutations (loss of heterozygosity [LOH] and microsatellite alterations) at the p53 gene were detected in CPAs (58%), and at somewhat lower frequencies at the RB gene (33%) and chromosomal location 5q (17%). Mutational frequency in the associated transitional and adenomatous areas were slightly lower than in the corresponding CPAs. No mutations were detected in adenomatous or transitional areas unless they also were present in the corresponding CPAs. Mutations of these three genes were absent in four cases of CPA, and in seven PAs without malignant change. These findings indicate that most CPAs arise from adenomas as the result of mutations in the three genes, especially p53. In addition, other, as yet unidentified genes may also be involved both in the development of PA and in its malignant progression to CPA. Mutational analysis of PAs may provide information of prognostic importance.
多形性腺瘤(PA)是涎腺最常见的良性肿瘤。多形性腺瘤中的癌(CPA)可能由PA的上皮成分恶变而来。偶尔,会发现一些过渡区域,其中的细胞具有介于良性PA和CPA癌性成分之间的组织学特征。在对存档的显微切片进行仔细显微切割后,作者研究了12例CPA及其伴随的腺瘤和过渡区域,检测p53、RB和K-ras基因以及染色体位点5q和9p的突变情况。作者未在K-ras基因或9p位点发现突变。在CPA中检测到p53基因有相对较高的突变率(杂合性缺失[LOH]和微卫星改变)(58%),在RB基因(33%)和染色体位置5q(17%)的突变频率略低。相关过渡区和腺瘤区的突变频率略低于相应的CPA。在腺瘤区或过渡区未检测到突变,除非相应的CPA中也存在这些突变。在4例CPA以及7例无恶变的PA中未检测到这三个基因的突变。这些发现表明,大多数CPA是由腺瘤因这三个基因尤其是p53的突变而产生的。此外,其他尚未明确的基因可能也参与了PA的发生及其向CPA的恶性进展。对PA进行突变分析可能会提供具有预后重要性的信息。