Lin Bo, Wang Qiujiao, Liu Kun, Dong Xu, Zhu Mingyue, Li Mengsen
Hainan Provincial Key Laboratory of Carcinogenesis and Intervention, Hainan Medical College, Haikou, China.
Institution of Tumor, Hainan Medical College, Haikou, China.
Front Oncol. 2021 Feb 25;11:625936. doi: 10.3389/fonc.2021.625936. eCollection 2021.
Alpha-fetoprotein (AFP) entrance into cancer cells is mediated by AFP receptors (AFPRs) and exerts malignant effects. Therefore, understanding the structure of AFPRs will facilitate the development of rational approaches for vaccine design, drug delivery, antagonizing immune suppression and diagnostic imaging to treat cancer effectively. Throughout the last three decades, the identification of universal receptors for AFP has failed due to their complex carbohydrate polymer structures. Here, we focused on the two types of binding proteins or receptors that may serve as AFPRs, namely, the A) mucin receptors family, and B) the scavenger family. We presented an informative review with detailed descriptions of the signal transduction, cross-talk, and interplay of various transcription factors which highlight the downstream events following AFP binding to mucin or scavenger receptors. We mainly explored the underlying mechanisms involved mucin or scavenger receptors that interact with AFP, provide more evidence to support these receptors as tumor AFPRs, and establish a theoretical basis for targeting therapy of cancer.
甲胎蛋白(AFP)进入癌细胞是由AFP受体(AFPRs)介导的,并发挥恶性作用。因此,了解AFPRs的结构将有助于开发合理的方法用于疫苗设计、药物递送、对抗免疫抑制和诊断成像,从而有效地治疗癌症。在过去三十年中,由于AFP的通用受体具有复杂的碳水化合物聚合物结构,对其识别一直未能成功。在此,我们聚焦于可能作为AFPRs的两种结合蛋白或受体,即A)粘蛋白受体家族和B)清道夫受体家族。我们进行了一项内容丰富的综述,详细描述了各种转录因子的信号转导、相互作用和相互影响,这些突出了AFP与粘蛋白或清道夫受体结合后的下游事件。我们主要探讨了与AFP相互作用的粘蛋白或清道夫受体所涉及的潜在机制,提供更多证据支持这些受体作为肿瘤AFPRs,并为癌症的靶向治疗建立理论基础。