Rogovskii Vladimir S
Department of molecular pharmacology and radiobiology, Pirogov Russian National Research Medical University, Moscow, Russia.
Curr Cancer Drug Targets. 2022;22(9):717-724. doi: 10.2174/1568009622666220602125343.
Urolithin A is the metabolite of natural polyphenol ellagic acid and ellagitannins generated by gut microbiota. Urolithin A is better absorbed in the gastrointestinal tract than its parent substances. Thus, the variable effects of ellagitannin-reach food (like pomegranate fruit, walnuts, tea, and others) on people's health might be linked with the differences in individual microbiota content. Urolithin A possesses various anti-inflammatory and anti-cancer effects, as shown by in vivo and in vitro studies.
In the current review, we consider anti-inflammatory and direct anti-cancer urolithin A effects as well as their molecular mechanisms, which might be the basement of clinical trials, estimating urolithin A anti-cancer effects.
Urolithin A attenuated the pro-inflammatory factors production (IL-6, IL-1β, NOS2 and others) in vitro studies. Oral urolithin A treatment caused prominent anti-cancer and anti-inflammatory action in various in vivo studies, including colitis rat model, carrageenan-induced paw edema mice model, models of pancreatic cancer, and models of obesity. The main molecular mechanisms of these effects might be the modulation of aryl hydrocarbon receptors, which antagonism may lead to decreasing of chronic inflammation. Other primary targets of urolithin A might be the processes of protein phosphorylation (for instance, it decreases the phosphorylation of protein kinase B) and p53 stabilization. Anti-inflammatory effects of urolithin A can be reached in physiologically relevant concentrations. This might be of vital importance for preventing immune suppression associated with chronic inflammation in cancer. Considering the favorable urolithin A safety profile, it is a promising compound for cancer treatment and prevention.
尿石素A是天然多酚鞣花酸和由肠道微生物群产生的鞣花单宁的代谢产物。尿石素A在胃肠道中的吸收比其母体物质更好。因此,富含鞣花单宁的食物(如石榴、核桃、茶等)对人体健康的不同影响可能与个体微生物群含量的差异有关。体内和体外研究表明,尿石素A具有多种抗炎和抗癌作用。
在本综述中,我们探讨尿石素A的抗炎和直接抗癌作用及其分子机制,这些可能是评估尿石素A抗癌作用的临床试验的基础。
在体外研究中,尿石素A可减少促炎因子的产生(如白细胞介素-6、白细胞介素-1β、一氧化氮合酶2等)。在各种体内研究中,包括结肠炎大鼠模型、角叉菜胶诱导的爪肿胀小鼠模型、胰腺癌模型和肥胖模型,口服尿石素A治疗具有显著的抗癌和抗炎作用。这些作用的主要分子机制可能是对芳烃受体的调节,其拮抗作用可能导致慢性炎症的减轻。尿石素A的其他主要作用靶点可能是蛋白质磷酸化过程(例如,它可降低蛋白激酶B的磷酸化)和p53的稳定。尿石素A在生理相关浓度下即可达到抗炎效果。这对于预防与癌症相关的慢性炎症引起的免疫抑制可能至关重要。鉴于尿石素A良好的安全性,它是一种有前景的癌症治疗和预防化合物。