Heppell-Parton A C, Nacheva E, Carter N P, Rabbitts P H
Medical Research Council Centre, Addenbrooke's Hospital, Cambridge, United Kingdom.
Cancer Genet Cytogenet. 1999 Jan 15;108(2):110-9. doi: 10.1016/s0165-4608(98)00130-7.
Until recently the ability to analyze complex karyotypic rearrangements was totally dependent upon light microscopy of G-banded chromosomes. Developments in the area of molecular cytogenetics have revolutionized such analysis, making it possible to determine the nature of complex rearrangements. An extensive analysis has been made of the small cell lung carcinoma (SCLC) cell line U2020, using a combined approach of conventional and molecular cytogenetics, enabling a highly detailed karyotype to be constructed revealing rearrangements previously undetected by G-banding alone. This approach offers the opportunity to reassess other tumor karyotypes, particularly those of high complexity found in solid tumors, for tumor-specific consistent rearrangements indecipherable by conventional karyotyping.
直到最近,分析复杂核型重排的能力完全依赖于G带染色体的光学显微镜检查。分子细胞遗传学领域的发展彻底改变了这种分析方法,使得确定复杂重排的性质成为可能。我们使用传统细胞遗传学和分子细胞遗传学相结合的方法,对小细胞肺癌(SCLC)细胞系U2020进行了广泛分析,从而构建了一个高度详细的核型,揭示了以前仅靠G带分析无法检测到的重排。这种方法为重新评估其他肿瘤核型提供了机会,特别是那些在实体瘤中发现的高度复杂的核型,以寻找传统核型分析无法解读的肿瘤特异性一致重排。