Vanni R, Lecca U, Faa G
Istituto di Biologia Generale, Sardinia, Italy.
Cancer Genet Cytogenet. 1991 Jun;53(2):247-56. doi: 10.1016/0165-4608(91)90101-y.
Chromosome analysis of 40 cultured uterine leiomyomas revealed the presence of clonal changes in 32.5% of them, confirming the cytogenetic heterogeneity within this type of tumor, mostly referable to a few cytogenetic subgroups. Preferential involvement of 12q14-15 and 14q23-24 bands in reciprocal and complex translocations was most commonly observed. Deletions of chromosome 7 and changes of chromosomes 1, 2, and to a lesser extent, chromosomes 19 and 22 were also found. Constitutional karyotype of patients bearing tumors with karyotypic abnormalities was examined. In one patient, two cells were found with t(12;14)(q14-15;q23-24) translocation and two with del(14)(q13q23-24). The latter rearrangement was also present as a clonal change in the tumor.
对40例培养的子宫平滑肌瘤进行染色体分析,结果显示其中32.5%存在克隆性改变,证实了这类肿瘤内的细胞遗传学异质性,多数可归因于少数细胞遗传学亚组。最常观察到12q14 - 15和14q23 - 24带在相互易位和复杂易位中优先受累。还发现了7号染色体缺失以及1、2号染色体改变,19和22号染色体改变程度较轻。对携带核型异常肿瘤患者的染色体组型进行了检查。在1例患者中,发现2个细胞存在t(12;14)(q14 - 15;q23 - 24)易位,2个细胞存在del(14)(q13q23 - 24)。后一种重排也作为肿瘤中的克隆性改变存在。