Chen Zixuan, Liu Min
Department of Urology, Tongren Hospital Shanghai Jiao Tong University School of Medicine, Shanghai 200336, China.
Biomolecules. 2025 Apr 25;15(5):620. doi: 10.3390/biom15050620.
Renal cell carcinoma (RCC) is the most lethal malignancy of the urinary system, with limited treatment options due to drug resistance and the adverse effects associated with current therapies. This review aims to systematically examine the therapeutic potential of flavonoids, which are natural polyphenolic compounds possessing anti-inflammatory, antioxidant, and anticancer properties, in the context of RCC treatment. We summarize the anticancer activities of 26 natural flavonoids, classified into six subclasses, and explore their mechanisms of action, including the inhibition of tumor cell proliferation, migration, and invasion, as well as the induction of apoptosis, autophagy, and ferroptosis. Particular attention is paid to their modulation of key signaling pathways such as the JAK/STAT3, PI3K/Akt/mTOR, and miRNA-related axes, including miR-21/YAP1 and miR-324-3p/GPX4, providing a molecular basis for their anti-RCC activity. We also address several pharmacological challenges that limit the clinical application of flavonoids, including poor bioavailability, metabolic instability, and potential toxicity. Emerging solutions such as novel flavonoid derivatives, advanced drug delivery systems, and rational combination therapy strategies are also discussed. Current clinical evidence, including a phase II trial of flavopiridol in advanced RCC, highlights the potential but also the need for further validation. In conclusion, flavonoids offer a promising approach to improving RCC treatment. Future research should focus on optimizing their therapeutic efficacy and ensuring their safe clinical translation, with the goal of achieving personalized and minimally invasive cancer therapies.
肾细胞癌(RCC)是泌尿系统中最致命的恶性肿瘤,由于耐药性以及当前治疗方法的不良反应,治疗选择有限。本综述旨在系统研究黄酮类化合物在RCC治疗中的治疗潜力,黄酮类化合物是具有抗炎、抗氧化和抗癌特性的天然多酚化合物。我们总结了26种天然黄酮类化合物的抗癌活性,这些化合物分为六个亚类,并探讨了它们的作用机制,包括抑制肿瘤细胞增殖、迁移和侵袭,以及诱导细胞凋亡、自噬和铁死亡。特别关注它们对关键信号通路的调节,如JAK/STAT3、PI3K/Akt/mTOR和与miRNA相关的轴,包括miR-21/YAP1和miR-324-3p/GPX4,为它们的抗RCC活性提供分子基础。我们还讨论了限制黄酮类化合物临床应用的几个药理学挑战,包括生物利用度差、代谢不稳定性和潜在毒性。还讨论了新型黄酮类衍生物、先进药物递送系统和合理联合治疗策略等新兴解决方案。目前的临床证据,包括黄酮哌醇治疗晚期RCC的II期试验,突出了其潜力,但也需要进一步验证。总之,黄酮类化合物为改善RCC治疗提供了一种有前景的方法。未来的研究应侧重于优化其治疗效果,并确保其安全的临床转化,目标是实现个性化和微创癌症治疗。