体和内细胞分裂:进入瘤细胞的途径
F M Dzarieva1, S A Pavlova1, G V Pavlova1
1Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences, 117485, Moscow, Russia; Federal State Autonomous Institution N. N. Burdenko National Medical Research Center of Neurosurgery of the Ministry of Health of the Russian Federation, 125047, Moscow, Russia.
Biochemical and biophysical research communications
|November 13, 2025
概括
阿普塔默在癌症治疗方面表现有前途,但在细胞进入方面存在困难. 这篇综述探讨了瘤细胞如何内化aptamer以及改善其传递以获得增强的抗瘤效果的策略.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 在瘤学瘤学.
背景情况:
- 胺是具有针对性治疗的高亲和度结合的DNA/RNA分子.
- 不高效的细胞吸收和细胞内贩运限制了阿帕特默在癌症治疗中的有效性.
研究的目的:
- 审查控制瘤细胞中aptamer内部化的内细胞通路.
- 讨论克服细胞内障碍和增强瘤学aptamer输送的策略.
主要方法:
- 关于阿帕特默内细胞分解机制的当前文献的综述.
- 对受体介导和受体独立内细胞通路的分析.
- 探索改善体细胞内命运和治疗结果的策略.
主要成果:
- 瘤微环境的特征,如EPR效应和受体过度表达,有利于体积累.
- 常见的内细胞路径包括克拉素依赖性,卡韦林依赖性,CLIC/GEEC,巨型内细胞和细胞.
- 在内体-溶酶体系统中捕获的aptamer阻碍了对细胞质点的访问.
结论:
- 了解阿普坦体内细胞分裂对于优化癌症治疗至关重要.
- 诸如化学修饰和纳米载体之类的策略可以增强aptamer的输送和有效性.
- 合理设计的aptamer平台可以提高特异性和治疗结果在瘤学.
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