He Hongye, Li Feng, Tang Rui, Wu Nianhong, Zhou Ying, Cao Yuting, Wang Can, Wan Li, Zhou Yang, Zhuang Hua, Li Pan
Institute of Ultrasound Imaging & Department of Ultrasound, The Second Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ultrasound Molecular Imaging, Chongqing 400010, China.
Department of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Biomater Res. 2024 Aug 13;28:0064. doi: 10.34133/bmr.0064. eCollection 2024.
Triple-negative breast cancer (TNBC) is a special subtype of breast cancer, which is highly aggressive and incurable. Here, we proposed an ultrasound activatable bromodomain-containing protein 4 (BRD4) proteolysis targeting chimera (PROTAC) release strategy for the first time for precisely controlled protein degradation in preclinical TNBC model. Through combination of PROTAC and ultrasound-targeted microbubble destruction (UTMD) technology, the present strategy also aims to concurrently solve the major limitations of poor loading capacity of microbubbles and undesirable targeting and membrane permeability of PROTAC. PROTAC (ARV-825)-encapsulated microbubbles, ARV-MBs, were developed for the efficacious treatment of TNBC in vitro and in vivo. The microbubbles we synthesized showed ultrasound-responsive drug release ability, which could effectively promote the penetration of PROTAC into tumor site and tumor cell. Under ultrasound, ARV-MBs could play an effective antitumor effect by potentiating the ubiquitination and degradation of BRD4 in tumor. The current study may provide a new idea for promoting clinical translation of drug-loaded microbubbles and PROTAC, and offer a new efficacious therapeutic modality for TNBC.
三阴性乳腺癌(TNBC)是乳腺癌的一种特殊亚型,具有高度侵袭性且难以治愈。在此,我们首次提出了一种超声可激活的含溴结构域蛋白4(BRD4)蛋白酶靶向嵌合体(PROTAC)释放策略,用于在临床前TNBC模型中精确控制蛋白质降解。通过将PROTAC与超声靶向微泡破坏(UTMD)技术相结合,本策略还旨在同时解决微泡负载能力差以及PROTAC靶向性和膜通透性不理想的主要局限性。为了在体外和体内有效治疗TNBC,研发了包裹有PROTAC(ARV-825)的微泡,即ARV-MBs。我们合成的微泡具有超声响应药物释放能力,可有效促进PROTAC渗透到肿瘤部位和肿瘤细胞中。在超声作用下,ARV-MBs可通过增强肿瘤中BRD4的泛素化和降解发挥有效的抗肿瘤作用。本研究可能为促进载药微泡和PROTAC的临床转化提供新思路,并为TNBC提供一种新的有效治疗方式。