Yosida T H
Cancer Genet Cytogenet. 1981 Apr;3(3):211-20. doi: 10.1016/0165-4608(81)90086-8.
In the Indian spiny mouse, Mus platythrix (2n = 26), six tumors were induced by 3-methylcholanthrene, and their karyotypes were analyzed in the primary state by G-banding. The chromosome numbers of these tumors were widely distributed ranging from diploid to tetraploid, but the frequency of cells exhibiting diploidy was the highest. Among these cells, the frequency of the cells with a normal diploid karyotype was only 27%, but the remaining cells (73%) showed pseudo- or near-diploid karyotypes. Although several numerical and structural anomalies of the chromosomes were observed in these tumor cells, centric fusion and translocation was most commonly seen, and that of trisomy and monosomy ranked second. Among 13 chromosome pairs, higher frequencies of chromosome anomalies were observed in the chromosomes No. 5, 8, and 12. Anomalies of the other autosomes were related primarily to centric fusion with chromosomes No, 5, 8, or 12, those of the X chromosome were mainly numerical changes. Taking into account the nucleolar organizer regions (NORs), which always occurred in chromosome pairs No. 5, 8 and 12 in this species, a possible relationship between the anomalies of those chromosomes containing NORs and the malignant transformation of cells is proposed.
在印度刺毛鼠(Mus platythrix,2n = 26)中,6个肿瘤由3-甲基胆蒽诱发,通过G显带对其核型进行了原代状态分析。这些肿瘤的染色体数目分布广泛,从二倍体到四倍体都有,但显示二倍体的细胞频率最高。在这些细胞中,具有正常二倍体核型的细胞频率仅为27%,但其余细胞(73%)显示假二倍体或近二倍体核型。尽管在这些肿瘤细胞中观察到了一些染色体的数目和结构异常,但着丝粒融合和易位最为常见,三体和单体异常位居第二。在13对染色体中,第5、8和12号染色体的染色体异常频率较高。其他常染色体的异常主要与与第5、8或12号染色体的着丝粒融合有关,X染色体的异常主要是数目变化。考虑到该物种中总是出现在第5、8和12号染色体对中的核仁组织区(NORs),提出了含有NORs的那些染色体异常与细胞恶性转化之间的可能关系。