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Complementation tagging of cooperating oncogenes in knockout mice.

作者信息

Allen J D, Berns A

机构信息

Division of Molecular Genetics, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

出版信息

Semin Cancer Biol. 1996 Oct;7(5):299-306. doi: 10.1006/scbi.1996.0038.

DOI:10.1006/scbi.1996.0038
PMID:9110407
Abstract

Gene disruption and overexpression in mice can be combined with proviral tagging to investigate the biochemical pathways in which oncogenes act. The phenomenon of oncogene collaboration permits a focussed genetic approach analogous to the strategies employed in suppressor screens in invertebrates and yeast. We illustrate here its application to investigating the action of the pim kinases in tumorigenesis. However, it should be possible to utilize this strategy for dissecting a much wider range of biochemical pathways in mammalian systems.

摘要

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Inhibition of PIM1 attenuates the stem cell-like traits of breast cancer cells by promoting RUNX3 nuclear retention.抑制 PIM1 通过促进 RUNX3 核保留来减弱乳腺癌细胞的干细胞样特征。
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The PIM-2 kinase is an essential component of the ultraviolet damage response that acts upstream to E2F-1 and ATM.
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