借力推动前列腺癌 CAR-T 细胞治疗进展
Piggybacking toward Progress for CAR T-Cell Therapy in Prostate Cancer.
P-PSMA-101 是一款首创的、富集干细胞记忆 T 细胞的、靶向前列腺特异性膜抗原(PSMA)的嵌合抗原受体(CAR)T 疗法。
英文原题:Targeting STEAP1 as an anticancer strategy.
尽管前列腺六跨膜上皮抗原 1(STEAP1)最初是在晚期前列腺癌中被发现,但其过表达已在多种类型的癌症中被确认,并与不良预后相关。
前列腺六跨膜上皮抗原1(STEAP1)最初在晚期前列腺癌中被发现,现已确认其在多种癌症中过表达,且与不良预后相关。由于具有肿瘤特异性并定位于细胞膜,STEAP1正成为备受关注的治疗靶点。一项I期试验证实,靶向STEAP1的抗体偶联药物在转移性去势抵抗性前列腺癌中具有临床疗效。此外,越来越多的证据表明,STEAP1也是免疫疗法(如CAR-T 细胞疗法)的理想靶点。本综述按癌症类型总结STEAP1的致癌功能,并就开发靶向STEAP1的新型抗癌策略提供新的见解。
Although the six-transmembrane epithelial antigen of prostate 1 (STEAP1) was first identified in advanced prostate cancer, its overexpression is recognized in multiple types of cancer and associated with a poor prognosis. STEAP1 is now drawing attention as a promising therapeutic target because of its tumor specificity and membrane-bound localization. The clinical efficacy of an antibody-drug conjugate targeting STEAP1 in metastatic, castration-resistant, prostate cancer was demonstrated in a phase 1 trial. Furthermore, growing evidence suggests that STEAP1 is an attractive target for immunotherapies such as chimeric antigen receptor-T cell therapy. In this review, we summarize the oncogenic functions of STEAP1 by cancer type. This review also provides new insights into the development of new anticancer strategies targeting STEAP1.
MEMBER ACCOUNT
登录成功会直接打开下一页。