摘要
前列腺癌 (PCa) 是全球主要的死亡原因之一。多种策略,包括手术、化学疗法、放射疗法和免疫疗法,被应用于 PCa 治疗。 PCa 细胞在早期阶段对治疗有反应,但它们可以在晚期获得抵抗力。此外,它们的迁移能力在晚期阶段很高。似乎遗传和表观遗传因素在这种情况下起着重要作用。锌指 E-box-binding homeobox (ZEB) 是一个转录家族,具有两个关键成员,包括 ZEB1 和 ZEB2。 ZEB 家族成员因参与通过 EMT 诱导促进癌症转移而闻名。最近的研究表明它们在癌症增殖和诱导治疗抵抗中的作用。在当前的审查中,我们重点揭示 ZEB1 和 ZEB2 在 PCa 中的作用。 ZEB 家族成员能够显着促进癌细胞的增殖和活力。 ZEB1 和 ZEB2 通过 EMT 诱导增强 PCa 细胞的迁移和侵袭。 ZEB1 和 ZEB2 的过表达与 PCa 的不良预后相关。 ZEB1 和 ZEB2 上调发生在 PCa 进展过程中,可以为癌细胞提供治疗抗性。 PRMT1、Smad2 和非编码 RNA 可以作为 ZEB 家族的上游介质。此外,Bax、Bcl-2、MRP1、Ncadherin 和 E-cadherin 可被视为 PCa 中 ZEB 家族的下游靶标。
关键词: 前列腺癌、锌指 E-box 结合同源框 (ZEB)、转移、化学抗性、增殖、上皮间质转化 (EMT)、microRNA、lncRNA。
图形摘要
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