Spectral karyotyping of the human colon cancer cell lines SW480 and SW620.

R Melcher, C Steinlein, W Feichtinger, C R Müller, T Menzel, H Lührs, W Scheppach, M Schmid
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引用次数: 18

Abstract

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.

人结肠癌细胞系SW480和SW620的光谱核型分析。
SW480和SW620细胞系来源于同一患者不同阶段的结肠癌,已被用于结肠癌的生化、免疫学和遗传学研究。对他们的核型进行比较分析,可以确定可能代表转移扩散标记的染色体畸变。本研究对这两种结肠癌细胞系进行了光谱核型分析。与先前报道的g带核型相比,9个(SW480)和7个(SW620)标记完全相同,3个(SW480)和3个(SW620)标记可以重新定义,5个(SW480)和8个(SW620)标记是新鉴定的,4个(SW480)和5个(SW620)标记无法确认。重新定义的像差包括非常复杂的重排,如der(16) t(3;16;1;16;8;16;1;16;10)和一个der(18)t(18;15;17)(q12;SW620中的p11p13;?? ?)和SW480中的der(19)t(19;8;19;5),这些都是传统条带技术无法识别的。在SW480和SW620中发现的染色体增益(5q11- >5q15, 7pter- >q22, 11,13q14 ->qter, 20pter- >p12, X)和缺失(8pter- >p2, 18q12- >qter, Y)与结直肠肿瘤中经常描述的干细胞原发变化非常一致。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的减少)可以被视为发生在推定的转移性创始细胞中的变化。
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