Division of Nuclear Medicine and Molecular Imaging, Department of Radiology and Radiological Science, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Nuclear Medicine Service, Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Sci Transl Med. 2016 Nov 30;8(367):367ra167. doi: 10.1126/scitranslmed.aaf2335.
Targeting the androgen receptor (AR) pathway prolongs survival in patients with prostate cancer, but resistance rapidly develops. Understanding this resistance is confounded by a lack of noninvasive means to assess AR activity in vivo. We report intracellular accumulation of a secreted antigen-targeted antibody (SATA) that can be used to characterize disease, guide therapy, and monitor response. AR-regulated human kallikrein-related peptidase 2 (free hK2) is a prostate tissue-specific antigen produced in prostate cancer and androgen-stimulated breast cancer cells. Fluorescent and radio conjugates of 11B6, an antibody targeting free hK2, are internalized and noninvasively report AR pathway activity in metastatic and genetically engineered models of cancer development and treatment. Uptake is mediated by a mechanism involving the neonatal Fc receptor. Humanized 11B6, which has undergone toxicological tests in nonhuman primates, has the potential to improve patient management in these cancers. Furthermore, cell-specific SATA uptake may have a broader use for molecularly guided diagnosis and therapy in other cancers.
靶向雄激素受体 (AR) 通路可延长前列腺癌患者的生存期,但耐药性很快就会出现。由于缺乏非侵入性的方法来评估体内 AR 活性,因此对这种耐药性的理解存在困难。我们报告了一种分泌型抗原靶向抗体 (SATA) 的细胞内积累,该抗体可用于表征疾病、指导治疗和监测反应。AR 调节的人激肽释放酶相关肽 2(游离 hK2)是一种前列腺组织特异性抗原,在前列腺癌和雄激素刺激的乳腺癌细胞中产生。针对游离 hK2 的抗体 11B6 的荧光和放射性缀合物可被内化,并在转移性和基因工程癌症发展和治疗模型中无创地报告 AR 通路活性。摄取是由一种涉及新生 Fc 受体的机制介导的。已经在非人类灵长类动物中进行了毒理学测试的人源化 11B6 有可能改善这些癌症患者的管理。此外,细胞特异性 SATA 摄取可能在其他癌症的分子指导诊断和治疗中具有更广泛的用途。