血液恶性瘤中的S100A8和S100A9:从发育到治疗
Farnaz Razmkhah1, Sena Kim1, Sora Lim1
1Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
International journal of molecular sciences
|September 9, 2023
概括
蛋白质S100A8和S100A9以及calprotectin通过改变骨髓微环境,显著影响血液恶性瘤. 它们显示出在整个癌症进展过程中作为诊断生物标志物和治疗点的潜力.
科学领域:
- 生物化学 生物化学
- 免疫学 免疫学 免疫学
- 在瘤学瘤学.
背景情况:
- S100A8和S100A9是多功能蛋白质,参与细胞信号传递和免疫细胞功能.
- 这些蛋白质在各种癌症中经常失调,包括血液性恶性瘤,影响疾病的进展和治疗反应.
研究的目的:
- 审查S100A8,S100A9和calprotectin在恶性骨髓微环境中的关键作用.
- 探索它们作为血液恶性瘤中的生物标志物和治疗点的潜力.
主要方法:
- 文献综述侧重于S100A8,S100A9和calprotectin的功能.
- 分析它们在血性恶性瘤相关的细胞过程中的参与.
- 检查它们的潜在临床应用.
主要成果:
- S100A8和S100A9调节细胞表型,影响活力,分化,化学敏感性和贩运.
- 由S100A8/S100A9异构体/异构四基体形成的calprotectin,积极促进恶性骨髓微环境.
- 这些蛋白质起着双重作用,可能驱动瘤发生或改善症状.
结论:
- 在血液恶性瘤中,S100A8,S100A9和calprotectin是塑造骨髓微环境的关键参与者.
- 它们在不同疾病阶段的参与凸显了它们从诊断到治疗的意义.
- 准这些蛋白质为血液癌症的新诊断和治疗策略提供了有希望的途径.
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