Oncogenic transformation of human cells: shortcomings of rodent model systems

被引:34
作者
Akagi, T [1 ]
机构
[1] Osaka Biosci Inst, Lab Mol Oncol, Suita, Osaka 5650874, Japan
关键词
D O I
10.1016/j.molmed.2004.09.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Long-standing difficulties in the in vitro transformation of human cells have been overcome. Using telomerase, several successful oncogene-mediated transformations of hum, an cells have been reported and the following cellular requirements for human cell transformation have been proposed: the maintenance of telomere sequences, the inactivation of Rb and p53 pathways, the perturbation of protein phosphatase 2A (PP2A) and the expression of activated Ras. Even when all of these requirements are fulfilled, however, the transformed phenotypes of human cells seem to be much less malignant than those of rodent cells meeting the same requirements. This suggests the existence of undefined cell-autonomous mechanisms that render human cells resistant to malignant transformation.
引用
收藏
页码:542 / 548
页数:7
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