In vivo activation of the p53 pathway by small-molecule antagonists of MDM2
- PMID: 14704432
- DOI: "VSports在线直播" 10.1126/science.1092472
"VSports手机版" In vivo activation of the p53 pathway by small-molecule antagonists of MDM2
Abstract
MDM2 binds the p53 tumor suppressor protein with high affinity and negatively modulates its transcriptional activity and stability. Overexpression of MDM2, found in many human tumors, effectively impairs p53 function. Inhibition of MDM2-p53 interaction can stabilize p53 and may offer a novel strategy for cancer therapy VSports手机版. Here, we identify potent and selective small-molecule antagonists of MDM2 and confirm their mode of action through the crystal structures of complexes. These compounds bind MDM2 in the p53-binding pocket and activate the p53 pathway in cancer cells, leading to cell cycle arrest, apoptosis, and growth inhibition of human tumor xenografts in nude mice. .
MeSH terms
- Actions (V体育平台登录)
- Actions (V体育安卓版)
- VSports在线直播 - Actions
- "VSports app下载" Actions
- "V体育官网" Actions
- VSports app下载 - Actions
- VSports最新版本 - Actions
- VSports注册入口 - Actions
- "VSports手机版" Actions
- "V体育安卓版" Actions
- "V体育官网" Actions
- VSports手机版 - Actions
- "V体育ios版" Actions
- Actions (VSports最新版本)
- Actions (VSports注册入口)
- "VSports" Actions
- "V体育ios版" Actions
- Actions (VSports app下载)
- V体育ios版 - Actions
- Actions (VSports在线直播)
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- "V体育ios版" Actions
- Actions (V体育平台登录)
- V体育2025版 - Actions
- Actions (V体育官网入口)
- Actions (V体育平台登录)
- V体育2025版 - Actions
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- Actions (V体育平台登录)
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