Department of Chemistry, Hunter College, City University of New York, New York, New York 10021, United States.
Ph.D. Program in Chemistry, The Graduate Center of the City University of New York, New York, New York 10016, United States.
Mol Pharm. 2020 Aug 3;17(8):3140-3147. doi: 10.1021/acs.molpharmaceut.0c00437. Epub 2020 Jul 16.
Ovarian cancer is the fifth leading cause of cancer deaths among women, accounting for more deaths than any other cancer of the female reproductive system. The foundation of its management consists of cytoreductive surgery (CRS) followed by systemic chemotherapy, with the completeness of surgical resection consistently identified as one of the most important prognostic factors for the disease. The goal of our investigation is the development of a near-infrared fluorescence (NIRF) imaging agent for the intraoperative imaging of high-grade serous ovarian cancer (HGSOC). As surgeons are currently limited to the visual and manual assessment of tumor tissue during CRS, this technology could facilitate more complete resections as well as serve important functions at other points in the surgical management of the disease. Elevated levels of cancer antigen 125 (CA125) have proven a useful biomarker of HGSOC, and the CA125-targeting antibody B43.13 has shown potential as a platform for immunoPET imaging in murine models of ovarian cancer. Herein, we report the development of a NIRF imaging agent based on B43.13: B43.13-IR800. We site-specifically modified the heavy chain glycans of B43.13 with the near-infrared dye IRDye 800CW using a chemoenzymatic approach developed in our laboratories. SDS-PAGE analysis confirmed the specificity of the conjugation reaction, and flow cytometry, immunostaining, and fluorescence microscopy verified the specific binding of B43.13-IR800 to CA125-expressing OVCAR3 human ovarian cancer cells. NIRF imaging studies demonstrated that B43.13-IR800 can be used to image CA125-expressing HGSOC tumors in subcutaneous, orthotopic, and patient-derived xenograft mouse models. Finally, analyses confirmed that B43.13-IR800 can bind and identify CA125-expressing cells in primary tumor and metastatic lymph node samples from human patients with HGSOC.
卵巢癌是女性癌症死亡的第五大主要原因,其死亡率高于女性生殖系统的任何其他癌症。其治疗的基础包括细胞减灭术(CRS),然后是全身化疗,手术切除的完整性一直被认为是疾病最重要的预后因素之一。我们研究的目的是开发一种用于高级别浆液性卵巢癌(HGSOC)术中成像的近红外荧光(NIRF)成像剂。由于外科医生目前在 CRS 期间仅限于对肿瘤组织进行视觉和手动评估,因此该技术可以促进更完全的切除,并在疾病的手术管理的其他方面发挥重要作用。癌症抗原 125(CA125)水平升高已被证明是 HGSOC 的有用生物标志物,并且 CA125 靶向抗体 B43.13 已显示出作为卵巢癌小鼠模型中免疫 PET 成像的平台的潜力。在此,我们报告了基于 B43.13 的 NIRF 成像剂的开发:B43.13-IR800。我们使用我们实验室开发的化学酶方法,特异性修饰了 B43.13 的重链聚糖与近红外染料 IRDye 800CW。SDS-PAGE 分析证实了缀合反应的特异性,流式细胞术、免疫染色和荧光显微镜验证了 B43.13-IR800 与表达 CA125 的 OVCAR3 人卵巢癌细胞的特异性结合。NIRF 成像研究表明,B43.13-IR800 可用于成像皮下、原位和患者来源的异种移植小鼠模型中表达 CA125 的 HGSOC 肿瘤。最后,分析证实 B43.13-IR800 可以结合并鉴定来自患有 HGSOC 的人类患者的原发性肿瘤和转移性淋巴结样本中的表达 CA125 的细胞。