癌症治疗相关心血管毒性的代谢重编程:机制和干预策略
Cheng Zeng1, Ying Gao2, Bo Lan1
1Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Seminars in cancer biology
|May 11, 2025
概括
癌症治疗可以通过改变新陈代谢来损害心脏 (心血管毒性). 了解这些代谢变化为在癌症治疗期间保护心脏健康提供了新的途径.
科学领域:
- 心血管医学 心血管医学
- 在瘤学瘤学.
- 代谢研究研究 代谢研究
背景情况:
- 与癌症治疗相关的心血管毒性 (CTR-CVT) 显著影响癌症幸存者的发病率和死亡率.
- CTR-CVT包括各种心脏问题,如心肌病,缺血,心律失常和血管功能障碍.
- 代谢重编程是癌症和心血管疾病的常见因素,但其在CTR-CVT中的作用尚不清楚.
研究的目的:
- 系统地审查癌症和心血管疾病中的代谢重编程.
- 分析抗癌疗法通过代谢变化诱导心血管毒性的机制.
- 探索针对CTR-CVT代谢失调的新型治疗策略.
主要方法:
- 系统的文献审查和当前研究的综合.
- 分析涉及癌症和心血管病理生理学的代谢途径.
- 评估新兴的针对代谢途径的治疗干预措施.
主要成果:
- 代谢重编程是癌症,心血管疾病和CTR-CVT之间的关键联系.
- 抗癌疗法可以通过特定的代谢干扰诱导心血管毒性.
- 准代谢途径是缓解CTR-CVT的一个有希望的策略.
结论:
- 对代谢重编程的更好理解对于解决CTR-CVT至关重要.
- 代谢干预可以改善癌症患者的心血管结果.
- 这一审查为开发更安全,更有效的癌症疗法提供了基础.
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