Centro de Investigación Príncipe Felipe, Valencia, Spain.
Centro de Biología Molecular Severo Ochoa, CSIC-UAM, Madrid, Spain.
Commun Biol. 2024 Aug 27;7(1):1053. doi: 10.1038/s42003-024-06689-2.
The placenta, a pivotal organ in mammalian reproduction, allows nutrient exchange and hormonal signaling between the mother and the developing fetus. Understanding its molecular intricacies is essential for deciphering normal embryonic development and pathological conditions such as tumorigenesis. Here, we explore the multifaceted role of the tumor suppressor BRCA1-associated protein 1 (BAP1) in cancer and placentation. Initially recognized for its tumor-suppressive properties, BAP1 has emerged as a key regulator at the intersection of tumorigenesis and placental development. BAP1 influences crucial cellular processes such as cell death, proliferation, metabolism, and response to hypoxic conditions. By integrating insights from tumor and developmental biology, we illuminate the complex molecular pathways orchestrated by BAP1. This perspective highlights BAP1's significant impact on both cancer and placental development, and suggests novel therapeutic strategies that could improve outcomes for pregnancy disorders and cancer.
胎盘是哺乳动物生殖中的关键器官,允许母体和发育中的胎儿之间进行营养物质交换和激素信号传递。理解其分子复杂性对于破译正常胚胎发育和肿瘤发生等病理状况至关重要。在这里,我们探讨了肿瘤抑制因子 BRCA1 相关蛋白 1(BAP1)在癌症和胎盘形成中的多方面作用。BAP1 最初因其肿瘤抑制特性而被认识,现已成为肿瘤发生和胎盘发育交汇点的关键调节剂。BAP1 影响着细胞死亡、增殖、代谢和对缺氧条件反应等关键细胞过程。通过整合肿瘤和发育生物学的见解,我们阐明了 BAP1 协调的复杂分子途径。这一观点强调了 BAP1 对癌症和胎盘发育的重大影响,并提出了新的治疗策略,可能改善妊娠疾病和癌症的预后。