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天然双黄酮类化合物在代谢相关疾病和癌症治疗中的生物活性。

Bioactivity of natural biflavonoids in metabolism-related disease and cancer therapies.

机构信息

Faculty of Pharmaceutical Sciences, Nagasaki International University, 2825-7 Huis Ten Bosch, Sasebo, Nagasaki 859-3298, Japan.

Department of Pharmacy, College of Pharmacy, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, South Korea.

出版信息

Pharmacol Res. 2021 May;167:105525. doi: 10.1016/j.phrs.2021.105525. Epub 2021 Mar 3.

Abstract

Natural biflavonoids, such as amentoflavone, bilobetin, ginkgetin, isoginkgetin, taiwaniaflavone, morelloflavone, delicaflavone, hinokiflavone, and other derivatives (~ 40 biflavonoids), are isolated from Selaginella sp., Ginkgo biloba, Garcinia sp., and several other species of plants. They are able to exert therapeutic benefits by regulating several proteins/enzymes (PPAR-γ, CCAAT/enhancer-binding protein α [C/EBPα], STAT5, pancreatic lipase, PTP1B, fatty acid synthase, α-glucosidase [AG]) and insulin signaling pathways (via PI3K-AKT), which are linked to metabolism, cell growth, and cell survival mechanisms. Deregulated insulin signaling can cause complications of obesity and diabetes, which can lead to cognitive disorders such as Alzheimer's, Parkinson's, and dementia; therefore, the therapeutic benefits of these biflavones in these areas are highlighted. Since biflavonoids have shown potential to regulate metabolism, growth- and survival-related protein/enzymes, their relation to tumor growth and metastasis of cancer associated with angiogenesis are highlighted. The translational role of biflavones in cancer with respect to the inhibition of metabolism-related processes/pathways, enzymes, or proteins, such as STAT3/SHP-1/PTEN, kinesins, tissue kallikreins, aromatase, estrogen, protein modifiers, antioxidant, autophagy, and apoptosis induction mechanisms, are discussed. Finally, considering their observed bioactivity potential, oral bioavailability studies of biflavones and related clinical trials are outlined.

摘要

天然双黄酮类化合物,如穗花杉双黄酮、bilobetin、银杏素、异银杏素、松双黄酮、杨梅素、delicaflavone、hinokiflavone 和其他衍生物(~40 种双黄酮),从卷柏属植物、银杏、藤黄属植物和其他几种植物中分离得到。它们能够通过调节几种蛋白质/酶(过氧化物酶体增殖物激活受体-γ、CCAAT/增强子结合蛋白α[C/EBPα]、STAT5、胰脂肪酶、PTP1B、脂肪酸合酶、α-葡萄糖苷酶[AG])和胰岛素信号通路(通过 PI3K-AKT)发挥治疗作用,这些通路与代谢、细胞生长和细胞存活机制有关。胰岛素信号的失调会导致肥胖和糖尿病的并发症,从而导致认知障碍,如阿尔茨海默病、帕金森病和痴呆症;因此,这些双黄酮在这些领域的治疗作用得到了强调。由于双黄酮类化合物显示出调节代谢、生长和存活相关蛋白质/酶的潜力,因此强调了它们与肿瘤生长和与血管生成相关的癌症转移的关系。双黄酮类化合物在癌症中的转化作用,涉及到抑制与代谢相关的过程/途径、酶或蛋白质,如 STAT3/SHP-1/PTEN、驱动蛋白、组织激肽、芳香酶、雌激素、蛋白质修饰剂、抗氧化剂、自噬和凋亡诱导机制,都进行了讨论。最后,考虑到它们观察到的生物活性潜力,概述了双黄酮及其相关临床试验的口服生物利用度研究。

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