Department of Biology, Faculty of Basic Science, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Department of Nutrition, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Prog Biophys Mol Biol. 2023 Jul-Aug;180-181:19-27. doi: 10.1016/j.pbiomolbio.2023.04.006. Epub 2023 Apr 18.
Natural substances are increasingly being used as cancer treatments. Scutellarin, as a flavonoid, recently has been identified in a Chinese herbal extract called Erigeron breviscapus (Vant.). Scutellarin is being researched for its potential benefits due to the discovery that it possesses a variety of biological effects, such as neuroprotective, anti-bacterial, and anti-viral properties. In addition to these biological functions, scutellarin has also been found to have anti-tumor properties. The underlying mechanisms of scutellarin's anticancer activity involve its ability to inhibit various signaling pathways, such as Jak/STAT, ERK/AMPK, and Wnt/β-catenin. Additionally, scutellarin activates intrinsic and extrinsic apoptotic pathways, which causes the death of tumor cells, interrupts the cell cycle, and promotes its arrest. By limiting metastasis, angiogenesis, drug resistance, and other tumorigenic processes, scutellarin also reduces the aggressiveness of tumors. Despite its promising anticancer activity, scutellarin faces several challenges in its clinical development, including poor solubility, bioavailability, and pharmacokinetic properties. Therefore, it has been suggested that certain modifications can enhance the pharmacogenetic capabilities of scutellarin to decrease its limited water solubility. In conclusion, scutellarin represents a potential candidate for cancer treatment and further studies are needed to explore its clinical utility and optimize its therapeutic potential.
天然物质越来越多地被用作癌症治疗方法。野黄芩苷是一种黄酮类化合物,最近在一种名为短葶飞蓬(Vant.)的中药提取物中被发现。由于发现它具有多种生物效应,如神经保护、抗菌和抗病毒特性,野黄芩苷正因其潜在的益处而受到研究。除了这些生物功能外,野黄芩苷还具有抗肿瘤特性。野黄芩苷抗癌活性的潜在机制包括其抑制各种信号通路的能力,如 Jak/STAT、ERK/AMPK 和 Wnt/β-catenin。此外,野黄芩苷激活内在和外在凋亡途径,导致肿瘤细胞死亡、中断细胞周期并促进其停滞。通过限制转移、血管生成、耐药性和其他肿瘤发生过程,野黄芩苷还降低了肿瘤的侵袭性。尽管野黄芩苷具有有希望的抗癌活性,但在其临床开发中仍面临一些挑战,包括溶解度差、生物利用度和药代动力学特性。因此,有人建议某些修饰可以增强野黄芩苷的遗传能力,以降低其有限的水溶性。总之,野黄芩苷是一种有潜力的癌症治疗候选药物,需要进一步研究来探索其临床应用并优化其治疗潜力。