Friedrich K, Scheithauer J, Dimmer V, Meyer W, Theissig F, Haroske G, Kunze K D
Institute of Pathology, University of Technology, Dresden, Germany.
Anal Cell Pathol. 2000;20(2-3):69-82. doi: 10.1155/2000/495102.
Chromosomal imbalances were analyzed in 62 breast cancers with different DNA ploidy by CGH. The results of DNA image cytometry and CGH are consistent with peridiploid and aneuploid cases. The peritetraploid tumors harbored a high number of chromosomal imbalances, as a hint for an unfavorable prognosis. The quantitative analysis of imbalances highlighted the role of different physical constituents of the chromosome, and of chromosomal losses in different DNA ploidy groups. The peritetraploid and aneuploid tumors differed from the peridiploid tumors in losses at 8p and 18q. The peritetraploid cancers exhibited more gains at 8q, the aneuploid tumors more losses at 17p than their peridiploid counterparts. The aneuploid cases differed from the peritetraploid tumors in a higher number of losses at 11q and 14q. Combinations of imbalances provide further insights into the genetic background of DNA ploidy. Hypotheses for the progression from peridiploid to nondiploid breast cancers are given.
通过比较基因组杂交(CGH)分析了62例具有不同DNA倍性的乳腺癌中的染色体失衡情况。DNA图像细胞术和CGH的结果与亚二倍体和非整倍体病例一致。四倍体肿瘤存在大量染色体失衡,提示预后不良。失衡的定量分析突出了染色体不同物理成分以及不同DNA倍性组中染色体缺失的作用。四倍体和非整倍体肿瘤在8p和18q缺失方面与亚二倍体肿瘤不同。四倍体癌症在8q处显示出更多的增益,非整倍体肿瘤在17p处的缺失比其亚二倍体对应物更多。非整倍体病例与四倍体肿瘤的不同之处在于11q和14q处有更多的缺失。失衡的组合为DNA倍性的遗传背景提供了进一步的见解。给出了从亚二倍体乳腺癌向非二倍体乳腺癌进展的假说。