Gardner H A, Gallie B L, Knight L A, Phillips R A
Cancer Genet Cytogenet. 1982 Jul;6(3):201-11. doi: 10.1016/0165-4608(82)90057-7.
There are conflicting reports on the frequency in retinoblastoma tumor cells of aberrations involving chromosome No. 13. To quantitate the frequency of various chromosome aberrations, we analyzed the karyotypes from the retinoblastoma tumors; all tumors contained chromosome abnormalities. Chromosome No. 13 was altered in only two tumors, but the aberrations in these two cases affected different portions of the chromosome. We have concluded that chromosome aberrations affecting chromosome No. 13 are relatively infrequent in retinoblastoma tumors. Chromosome No.1 was involved in rearrangements in eight tumors; in six tumors the rearrangements lead to trisomy of 1q25-1q32. Seven tumors had aberrations resulting in trisomy of the long arm of chromosome No. 17; the most common aberration was an i(17q) chromosome. Every tumor showed trisomy of the long arm of either chromosome No. 1 or 17. These changes in chromosomes No. 1 and 17 have been observed by others in many different tumors and are not unique to retinoblastoma. In summary, chromosome abnormalities were present in all retinoblastoma tumors studied, but no aberration common to all tumors was found.
关于视网膜母细胞瘤肿瘤细胞中涉及13号染色体的畸变频率,存在相互矛盾的报道。为了定量各种染色体畸变的频率,我们分析了视网膜母细胞瘤肿瘤的核型;所有肿瘤都含有染色体异常。只有两个肿瘤中的13号染色体发生了改变,但这两例中的畸变影响了染色体的不同部分。我们得出结论,影响13号染色体的染色体畸变在视网膜母细胞瘤肿瘤中相对少见。1号染色体在八个肿瘤中参与了重排;在六个肿瘤中,重排导致1q25 - 1q32三体。七个肿瘤存在导致17号染色体长臂三体的畸变;最常见的畸变是i(17q)染色体。每个肿瘤都显示1号或17号染色体长臂三体。1号和17号染色体的这些变化在许多不同肿瘤中都被其他人观察到,并非视网膜母细胞瘤所特有。总之,在所研究的所有视网膜母细胞瘤肿瘤中都存在染色体异常,但未发现所有肿瘤共有的畸变。