Department of Pathology, Duke University School of Medicine, Durham, NC, USA.
Department of Data Science, Dana-Farber Cancer Institute, Boston, MA, USA.
J Pathol. 2023 May;260(1):43-55. doi: 10.1002/path.6063. Epub 2023 Mar 14.
Neuroendocrine (NE) cells comprise ~1% of epithelial cells in benign prostate and prostatic adenocarcinoma (PCa). However, they become enriched in hormonally treated and castration-resistant PCa (CRPC). In addition, close to 20% of hormonally treated tumors recur as small cell NE carcinoma (SCNC), composed entirely of NE cells, which may be the result of clonal expansion or lineage plasticity. Since NE cells do not express androgen receptors (ARs), they are resistant to hormonal therapy and contribute to therapy failure. Here, we describe the identification of glypican-3 (GPC3) as an oncofetal cell surface protein specific to NE cells in prostate cancer. Functional studies revealed that GPC3 is critical to the viability of NE tumor cells and tumors displaying NE differentiation and that it regulates calcium homeostasis and signaling. Since our results demonstrate that GPC3 is specifically expressed by NE cells, patients with confirmed SCNC may qualify for GPC3-targeted therapy which has been developed in the context of liver cancer and displays minimal toxicity due to its tumor-specific expression. © 2023 The Pathological Society of Great Britain and Ireland.
神经内分泌 (NE) 细胞约占良性前列腺和前列腺腺癌 (PCa) 上皮细胞的 1%。然而,它们在激素治疗和去势抵抗性 PCa (CRPC) 中变得丰富。此外,近 20%的激素治疗肿瘤复发为完全由 NE 细胞组成的小细胞神经内分泌癌 (SCNC),这可能是克隆扩张或谱系可塑性的结果。由于 NE 细胞不表达雄激素受体 (ARs),它们对激素治疗有抵抗力,并导致治疗失败。在这里,我们描述了糖蛋白 3 (GPC3) 的鉴定,它是前列腺癌中 NE 细胞的一种癌胚细胞表面蛋白。功能研究表明,GPC3 对 NE 肿瘤细胞和显示 NE 分化的肿瘤的存活至关重要,并且它调节钙稳态和信号转导。由于我们的结果表明 GPC3 仅由 NE 细胞特异性表达,因此已被确认为 SCNC 的患者可能有资格接受 GPC3 靶向治疗,该治疗已在肝癌背景下开发,并因其肿瘤特异性表达而显示出最小的毒性。 2023 年英国和爱尔兰病理学学会。