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发现具有内在荧光的靶向雌激素受体α(ERα)的蛋白降解靶向嵌合体(PROTACs)用于乳腺癌的精准诊疗。

Discovery of ERα-targeting PROTACs with intrinsic fluorescence for precision theranostics of breast cancer.

作者信息

Wu Yihe, Dai Junhong, Deng Xiaofei, He Pei, Liang Jinsen, Xin Lilan, Xie Baohua, Zhu Shenghong, Dong Chune, Zhou Hai-Bing

机构信息

Department of Hematology, Zhongnan Hospital of Wuhan University, School of Pharmaceutical Sciences, Wuhan University Wuhan 430071 China

Yangtze River Pharmaceutical Group JiangSu Haici Biological Pharmaceutical Co., Ltd. 8 Taizhen Road, Medical New & Hi-tech Industrial Development Zone Taizhou 225321 China.

出版信息

RSC Med Chem. 2025 May 22. doi: 10.1039/d5md00281h.

Abstract

Real-time monitoring of protein degradation is challenging. Herein, novel ERα-targeted dual-function PROTACs with intrinsic fluorescence were designed and synthesized for precision theranostics of breast cancer. Among them, W2 showed good antiproliferative activity, selective ERα degradation and imaging capabilities in MCF-7 breast cancer cell lines. The safety assay indicated that W2 was well-tolerated up to a dose of 500 mg kg with no acute toxicity. This work demonstrates the great potential of ERα-targeted PROTACs as theranostic agents in breast cancer treatment.

摘要

蛋白质降解的实时监测具有挑战性。在此,设计并合成了具有内在荧光的新型ERα靶向双功能PROTACs,用于乳腺癌的精准诊疗。其中,W2在MCF-7乳腺癌细胞系中表现出良好的抗增殖活性、选择性ERα降解和成像能力。安全性试验表明,W2在高达500 mg/kg的剂量下耐受性良好,无急性毒性。这项工作证明了ERα靶向PROTACs作为乳腺癌治疗中诊疗药物的巨大潜力。

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