Novel Theranostic Targets for Prostate Cancer Beyond Prostate-Specific Membrane Antigen.

Pedram Heidari, Hossein Jadvar, Bashar Kako, Shadi A Esfahani
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引用次数: 0

Abstract

Prostate-specific membrane antigen (PSMA)-targeted theranostics have transformed prostate cancer management, but some tumors exhibit low or heterogeneous PSMA expression, limiting eligibility and efficacy for radiopharmaceutical therapy. This review explores emerging biomarkers that may complement or expand beyond PSMA, including gastrin-releasing peptide receptor, fibroblast activation protein, prostate stem cell antigen, CD46, delta-like ligand 3, glypican-3, B7-H3, 6-transmembrane epithelial antigen of the prostate-1, trophoblast cell surface antigen-2, CEACAM5, and vicrostatin. We review their molecular biology, preclinical validation, clinical translation, and ongoing trials. These biomarkers represent diverse biological compartments, broadening the scope of precision radiotheranostics for prostate cancer.

前列腺特异性膜抗原以外的前列腺癌新治疗靶点。
前列腺特异性膜抗原(PSMA)靶向治疗已经改变了前列腺癌的治疗方法,但一些肿瘤表现出低水平或异质性的PSMA表达,限制了放射性药物治疗的资格和疗效。本综述探讨了可能补充或扩展PSMA的新兴生物标志物,包括胃泌素释放肽受体、成纤维细胞活化蛋白、前列腺干细胞抗原、CD46、δ样配体3、glypican-3、B7-H3、6-前列腺-1跨膜上皮抗原、滋养细胞表面抗原-2、CEACAM5和维罗他汀。我们回顾了它们的分子生物学、临床前验证、临床翻译和正在进行的试验。这些生物标志物代表了不同的生物区室,扩大了前列腺癌精确放射治疗的范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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