Melcher R, Steinlein C, Feichtinger W, Müller C R, Menzel T, Lührs H, Scheppach W, Schmid M
Institute of Human Genetics, University of Würzburg, Germany.
Cytogenet Cell Genet. 2000;88(1-2):145-52. doi: 10.1159/000015508.
The cell lines SW480 and SW620, derived from different stages of colon carcinoma in the same patient, have been used for a number of biochemical, immunological, and genetic studies on colon cancer. A comparative analysis of their karyotypes may identify chromosomal aberrations that might represent markers for metastatic spread. In the present study spectral karyotyping (SKY) was applied to these two colon cancer cell lines. Compared to previously reported G-banded karyotypes, 9 (SW480) and 7 (SW620) markers were identical, 3 (SW480) and 3 (SW620) markers could be redefined, 5 (SW480) and 8 (SW620) markers were newly identified, and 4 (SW480) and 5 (SW620) of the previous described markers could not be confirmed. The redefined aberrations include very complex rearrangements, such as a der(16) t(3;16;1;16;8;16; 1;16;10) and a der(18)t(18;15;17)(q12; p11p13;??) in SW620 and a der(19)t(19;8;19;5) in SW480, that have not been identified by conventional banding techniques. The resulting chromosome gains (5q11-->5q15, 7pter-->q22, 11, 13q14-->qter, 20pter-->p12, X) and losses (8pter-->p2, 18q12-->qter, Y) found in both SW480 and SW620 were in good agreement with those frequently described in colorectal tumors as primary changes in the stem cell. Abnormalities found exclusively in SW620 cells only (gains of 5pter-->5q11, 12q12-->q23, 15p13-->p11, and 16q21-->q24 and losses of 2pter-->2p24, 4q28-->qter, and 6q25-->qter) can be viewed as changes that occurred in a putative metastatic founder cell.
SW480和SW620这两种细胞系源自同一患者结肠癌的不同阶段,已被用于多项关于结肠癌的生化、免疫和遗传学研究。对它们的核型进行比较分析,可能会识别出可能代表转移扩散标志物的染色体畸变。在本研究中,光谱核型分析(SKY)被应用于这两种结肠癌细胞系。与先前报道的G带核型相比,9个(SW480)和7个(SW620)标记是相同的,3个(SW480)和3个(SW620)标记可以重新定义,5个(SW480)和8个(SW620)标记是新发现的,并且先前描述的4个(SW480)和5个(SW620)标记无法得到证实。重新定义的畸变包括非常复杂的重排,例如SW620中的der(16)t(3;16;1;16;8;16; 1;16;10)和der(18)t(18;15;17)(q12; p11p13;??)以及SW480中的der(19)t(19;8;19;5),这些畸变是传统带型技术未识别出的。在SW480和SW620中都发现的染色体增加(5q11→5q15、7pter→q22、11、13q14→qter、20pter→p12、X)和缺失(8pter→p2、18q12→qter、Y)与在结直肠肿瘤中经常描述的作为干细胞主要变化的情况高度一致。仅在SW620细胞中发现的异常(5pter→5q11、12q12→q23、15p13→p11和16q21→q24的增加以及2pter→2p24、4q28→qter和6q25→qter的缺失)可被视为在假定的转移起始细胞中发生的变化。