Chen Yamei, Liu Xuwei, Sun Yang, Liu Keying, Ding Ding, Song Shaoli, Tan Weihong
Institute of Molecular Medicine (IMM), Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200240, China.
Department of Nuclear Medicine, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
J Nanobiotechnology. 2025 Mar 6;23(1):182. doi: 10.1186/s12951-025-03184-6.
Recent advancements in antibody-drug conjugates (ADCs) targeting trophoblast surface cell antigen 2 (Trop-2) have brought important progress in the field of targeted therapy. This progress also holds promise for the treatment of small cell lung cancer (SCLC) as anti-Trop-2 therapy appears to have a safe and effective clinical activity in metastatic SCLC patients. However, effective treatments of anti-Trop-2 ADCs rely on the comprehensive assessment of Trop-2 expression at the tumor sites, SCLC exhibits intratumoral heterogeneity, making the accurate acquisition of histological biopsies a challenge. To address this issue, we herein report the development of an anti-Trop-2 aptamer consisting of 76 bases is specifically bind to Trop-2-overexpressing SCLC cells. Further truncated anti-Trop-2 aptamer with 46 nucleotides also possesses excellent in vitro and in vivo binding affinity with Trop-2 antigens. After radiolabeling with gallium-68 radionuclide, an aptamer-based molecular imaging probe was successfully fabricated named [Ga]Ga-NOTA-TRP-c. This imaging probe demonstrated effective and precise differentiation of Trop-2-positive tumors in both murine- and human-derived animal models, exhibiting favorable metabolic profiles. Furthermore, Trop-2-positive SCLC tumors recognized by anti-Trop-2 aptamer can be treated with anti-Trop-2 ADC sacituzumab govitecan (SG), either in vitro or in vivo. Importantly, SG induces DNA damage and cell apoptosis without affecting the expression of Trop-2 on the cell surface, which makes it possible to use anti-Trop-2 aptamer to monitor the expression of Trop-2 in SCLC. This study highlights the potential of aptamer-based molecular imaging and imaging-guided SG treatment as a promising option for targeted therapy in SCLC.
靶向滋养层表面细胞抗原2(Trop-2)的抗体药物偶联物(ADC)的最新进展在靶向治疗领域取得了重要进展。这一进展也为小细胞肺癌(SCLC)的治疗带来了希望,因为抗Trop-2疗法在转移性SCLC患者中似乎具有安全有效的临床活性。然而,抗Trop-2 ADC的有效治疗依赖于对肿瘤部位Trop-2表达的全面评估,SCLC存在肿瘤内异质性,使得准确获取组织活检成为一项挑战。为了解决这个问题,我们在此报告了一种由76个碱基组成的抗Trop-2适配体的开发,该适配体特异性结合过表达Trop-2的SCLC细胞。进一步截短的含有46个核苷酸的抗Trop-2适配体也与Trop-2抗原具有优异的体外和体内结合亲和力。在用镓-68放射性核素进行放射性标记后,成功制备了一种基于适配体的分子成像探针,名为[Ga]Ga-NOTA-TRP-c。该成像探针在小鼠和人源动物模型中均能有效且精确地区分Trop-2阳性肿瘤,显示出良好的代谢特征。此外,抗Trop-2适配体识别的Trop-2阳性SCLC肿瘤在体外或体内均可使用抗Trop-2 ADC赛托珠单抗戈维汀(SG)进行治疗。重要的是,SG诱导DNA损伤和细胞凋亡,而不影响细胞表面Trop-2的表达,这使得使用抗Trop-2适配体监测SCLC中Trop-2的表达成为可能。这项研究强调了基于适配体的分子成像和成像引导的SG治疗作为SCLC靶向治疗的一种有前景选择的潜力。