Memorial Cancer Institute, Pembroke Pines, FL 33028, USA.
Int J Mol Sci. 2024 Jan 15;25(2):1046. doi: 10.3390/ijms25021046.
Folate receptor α (FR) was discovered many decades ago, along with drugs that target intracellular folate metabolism, such as pemetrexed and methotrexate. Folate is taken up by the cell via this receptor, which also targeted by many cancer agents due to the over-expression of the receptor by cancer cells. FR is a membrane-bound glycosyl-phosphatidylinositol (GPI) anchor glycoprotein encoded by the folate receptor 1 (FOLR1) gene. FR plays a significant role in DNA synthesis, cell proliferation, DNA repair, and intracellular signaling, all of which are essential for tumorigenesis. FR is more prevalent in cancer cells compared to normal tissues, which makes it an excellent target for oncologic therapeutics. FRα is found in many cancer types, including ovarian cancer, non-small-cell lung cancer (NSCLC), and colon cancer. FR is widely used in antibody drug conjugates, small-molecule-drug conjugates, and chimeric antigen-receptor T cells. Current oncolytic therapeutics include mirvetuximab soravtansine, and ongoing clinical trials are underway to investigate chimeric antigen receptor T cells (CAR-T cells) and vaccines. Additionally, FRα has been used in a myriad of other applications, including as a tool in the identification of tumor types, and as a prognostic marker, as a surrogate of chemotherapy resistance. As such, FRα identification has become an essential part of precision medicine.
叶酸受体 α(FR)是几十年前与靶向细胞内叶酸代谢的药物一起发现的,例如培美曲塞和甲氨蝶呤。叶酸通过该受体被细胞摄取,由于癌细胞过度表达受体,许多癌症药物也靶向该受体。FR 是一种膜结合糖基磷脂酰肌醇(GPI)锚定糖蛋白,由叶酸受体 1(FOLR1)基因编码。FR 在 DNA 合成、细胞增殖、DNA 修复和细胞内信号传导中发挥重要作用,所有这些都是肿瘤发生所必需的。与正常组织相比,FR 在癌细胞中更为普遍,这使其成为肿瘤治疗的理想靶点。FRα存在于许多癌症类型中,包括卵巢癌、非小细胞肺癌(NSCLC)和结肠癌。FR 广泛用于抗体药物偶联物、小分子药物偶联物和嵌合抗原受体 T 细胞。目前的溶瘤治疗包括 mirvetuximab soravtansine,正在进行临床试验以研究嵌合抗原受体 T 细胞(CAR-T 细胞)和疫苗。此外,FRα 还在许多其他应用中得到了应用,包括作为鉴定肿瘤类型的工具以及作为预后标志物,作为化疗耐药的替代标志物。因此,FRα 的鉴定已成为精准医学的重要组成部分。