Sreekantaiah C, Sandberg A A
Cancer Center of Southwest Biomedical Research Institute, Scottsdale, Arizona.
Int J Cancer. 1991 May 10;48(2):194-8. doi: 10.1002/ijc.2910480207.
Cytogenetic analyses of benign tumors in the past 2 decades have established consistent and recurrent abnormalities in a large proportion of these tumors. In particular, chromosomal analyses of meningiomas, adenomas of the salivary gland, uterine leiomyomas and lipomas have led to the identification of cytogenetic subtypes characterized by specific structural or numerical abnormalities. A comparison of these consistent changes shows a clustering of aberrations to specific regions on chromosomes 12, 1, 2, 6, 11, 13 and 22. The specificity of the involvement of these chromosome regions in the various benign neoplasms suggests that genes of importance in growth regulation rather than those related to malignant transformation are located at these sites.
在过去20年中,对良性肿瘤的细胞遗传学分析已证实在这些肿瘤的很大一部分中存在一致且反复出现的异常。特别是,对脑膜瘤、涎腺腺瘤、子宫平滑肌瘤和脂肪瘤的染色体分析已导致识别出以特定结构或数量异常为特征的细胞遗传学亚型。对这些一致变化的比较显示,畸变聚集在染色体12、1、2、6、11、13和22的特定区域。这些染色体区域在各种良性肿瘤中的参与特异性表明,在生长调节中重要的基因而非与恶性转化相关的基因位于这些位点。