Verschaeve L, Verschueren H, VandenDriessche T, van Hecke D, Verhaegen S, de Baetselier P
Laboratorium voor Antropogenetica, Vrije Universiteit Brussel, Belgium.
Genes Chromosomes Cancer. 1989 Nov;1(2):119-30. doi: 10.1002/gcc.2870010203.
Cell lines differing in their malignant potential have been derived from the murine BW5147 T-cell lymphosarcoma. To evaluate the involvement of chromosomal aberrations in tumor progression within this model, we have analyzed the karyotypes and the in vitro invasiveness of 13 related nonmetastatic and metastatic variants. Giemsa banding revealed the presence of several marker chromosomes, one of which was of particular importance. Depending on the cell line, four variants of this marker I were found: Marker Ia corresponds to two translocated chromosomes 3, marker Ib is a deleted Ia marker, marker Ic is a Ib translocated to small unidentified chromosome fragment, and marker Id is a further deleted Ib marker. The Ia and Id markers were characteristic for the noninvasive, nonmetastatic lines, whereas the Ib and Ic markers predominated in the invasive, metastatic variants. The results suggest that metastasis-enhancing genes are located between the D and FI band of mouse chromosome 3 and that metastasis-suppressing genes are located between the FI and H band of the same chromosome.
具有不同恶性潜能的细胞系源自小鼠BW5147 T细胞淋巴瘤。为了评估该模型中染色体畸变在肿瘤进展中的作用,我们分析了13个相关的非转移性和转移性变体的核型及体外侵袭性。吉姆萨显带显示存在几条标记染色体,其中一条尤为重要。根据细胞系的不同,发现了这种标记I的四种变体:标记Ia对应两条易位的3号染色体,标记Ib是缺失的Ia标记,标记Ic是易位到小的未识别染色体片段的Ib,标记Id是进一步缺失的Ib标记。Ia和Id标记是非侵袭性、非转移性细胞系的特征,而Ib和Ic标记在侵袭性、转移性变体中占主导。结果表明,转移增强基因位于小鼠3号染色体的D和FI带之间,转移抑制基因位于同一染色体的FI和H带之间。