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Genetic Complementation of the Immortal Phenotype in Group D Cell Lines by Introduction of Chromosome 7
Human immortal cell lines have been classified into at least four (A–D) genetic complementation groups by cell‐cell hybrid analysis, i.e., a hybrid derived from different groups becomes mortal. Recently we have demonstrated that introduction of human chromosome 7 suppresses indefinite division poten...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1995
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920584/ https://www.ncbi.nlm.nih.gov/pubmed/7737907 http://dx.doi.org/10.1111/j.1349-7006.1995.tb02985.x |
Sumario: | Human immortal cell lines have been classified into at least four (A–D) genetic complementation groups by cell‐cell hybrid analysis, i.e., a hybrid derived from different groups becomes mortal. Recently we have demonstrated that introduction of human chromosome 7 suppresses indefinite division potential in the non‐tumorigenic human immortalized fibroblast lines KMST‐6 and SUSM‐1, both assigned to complementation group D. By extending our microcell‐mediated chromosome transfer, we found that chromosome 7 also suppresses division potential in the human hepatoma line HepG2 (again, assigned to group D). Chromosome 7 was thus shown to suppress indefinite growth in the above group D cell lines irrespective of their cell types, or whether they are tumorigenic or not. Since chromosome 7 had no such effect on representative cell lines derived from complementation group A, B or C, these results indicate that the senescence gene(s) commonly mutated in the group D cell lines is located on chromosome 7. |
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