时间标签:数据日期 2026-11-05 · 生成时间 2026-11-05 05:30(Asia/Shanghai)| 检索窗口 PubMed edat 2026/11/02 – 2026/11/06 | 情报发生日期 2026-11-05
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摘要(PubMed 原文节选)
Autophagy and ferroptosis are evolutionarily conserved stress-response pathways that critically regulate tumor progression and therapeutic responsiveness. In breast cancer, the autophagy initiator Beclin-1 acts as a haploinsufficient tumor suppressor, whereas susceptibility to ferroptosis is largely governed by the GPX4-SLC7A11-TFRC redox…
对本项目的价值
参考价值:属「营养感知—自噬—蛋白稳态轴」方向;mTOR / 自噬 / 蛋白质稳态栏目可用作本项目文献库与综述素材。 | 价值分 1.8/5(★★☆☆☆)
全文不可及原因
无 PMCID 且 Europe PMC / OpenAlex / Unpaywall 未提供可下载 OA 全文
原文题录
- 中文题名:氧代吡咯烷-酰腙骨架经 JNK/Beclin-1/GPX4 调控成为乳腺癌自噬与铁死亡双重诱导剂
- 英文标题:Oxopyrrolidine-Acylhydrazone Scaffolds as Dual Inducers of Autophagy and Ferroptosis in the Breast Cancer via JNK/Beclin-1/GPX4 Regulation.
- 期刊与标识:Drug development research · PMID 42974699 · DOI 10.1002/ddr.70401