The incidence of androgen receptor (AR)-negative (AR(-)) prostate cancer, including aggressive neuroendocrine prostate cancer (NEPC), has more than doubled in the last decade, but its timely diagnosis is difficult as it lacks typical prostate cancer hallmarks. The carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5) has recently been identified as an upregulated surface antigen in NEPC. We developed an immuno-PET agent targeting CEACAM5 and evaluated its ability to delineate AR(-) prostate cancer in vivo. Methods: CEACAM5 expression was evaluated in a panel of prostate cancer cell lines by immunohistochemistry and Western blotting. The CEACAM5-targeting antibody labetuzumab was conjugated with the chelator desferrioxamine (DFO) and radiolabeled with (89)Zr. The in vivo distribution of the radiolabeled antibody was evaluated in xenograft prostate cancer models by PET imaging and ex vivo organ distribution. Results: The NEPC cell line H660 exhibited strong CEACAM5 expression, whereas expression was limited in the AR(-) cell lines PC3 and DU145 and absent in the AR-positive cell line LNCaP. [(89)Zr]Zr-DFO-labetuzumab imaging was able to clearly delineate both neuroendocrine H660 xenografts and AR(-) DU145 in vivo but could not detect the AR-positive xenograft LNCaP. Conclusion: Immuno-PET imaging with [(89)Zr]Zr-DFO-labetuzumab is a promising diagnostic tool for AR(-) prostate cancer.
CEACAM5-Targeted Immuno-PET in Androgen Receptor-Negative Prostate Cancer.
CEACAM5靶向免疫PET在雄激素受体阴性前列腺癌中的应用
阅读:15
作者:Imberti Cinzia, De Gregorio Roberto, Korsen Joshua A, Hoang Tran T, Khitrov Samantha, Kalidindi Teja, Nandakumar Subhiksha, Park Jooyoung, Zaidi Samir, Pillarsetty Naga Vara Kishore, Lewis Jason S
| 期刊: | Journal of Nuclear Medicine | 影响因子: | 9.100 |
| 时间: | 2024 | 起止号: | 2024 Jul 1; 65(7):1043-1050 |
| doi: | 10.2967/jnumed.123.267107 | 研究方向: | 免疫/内分泌 |
| 疾病类型: | 前列腺癌 | ||
特别声明
1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。
2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。
3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。
4、投稿及合作请联系:info@biocloudy.com。
