Wu Yihe, Dai Junhong, Deng Xiaofei, He Pei, Liang Jinsen, Xin Lilan, Xie Baohua, Zhu Shenghong, Dong Chune, Zhou Hai-Bing
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.
RSC Med Chem. 2025 May 22. doi: 10.1039/d5md00281h.
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.
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。