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p53 and MDM2: Antagonists or Partners in Crime?

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CANCER CELL
卷 15, 期 3, 页码 161-162

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CELL PRESS
DOI: 10.1016/j.ccr.2009.02.004

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Therapeutics that disrupt the p53-MDM2 interaction show promise for cancer treatment but surprisingly have different biological outcomes. A study by Enge et al. in this issue of Cancer Cell shows that the ability of MDM2 to target hnRNP K for degradation contributes to the decision to induce apoptosis rather than cell-cycle arrest.

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