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首页> 外文期刊>Biochemical Pharmacology >UNBS1450 from Calotropis procera as a regulator of signaling pathways involved in proliferation and cell death.
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UNBS1450 from Calotropis procera as a regulator of signaling pathways involved in proliferation and cell death.

机译:来自Calotropis procera的UNBS1450作为涉及增殖和细胞死亡的信号通路的调节剂。

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摘要

Despite significant progress in oncology therapeutics in the last decades, the urge to discover and to develop new, alternative or synergistic anti-cancer agents still remains. For centuries it has been known that the coarse shrub Calotropis procera is a very promising source of ascaricidal, schizonticidal, anti-bacterial, anthelmintic, insecticidal, anti-inflammatory, anti-diarrhoeal, larvicidal and cytotoxic chemicals. Different compounds like norditerpenic esters, organic carbonates, the cysteine protease procerain, alkaloids, flavonoids, sterols as well as numerous types of cardenolides have provided this plant for centuries with scientists' interest. The chemical class of cardenolides and their related bioactivity evaluation and structure-activity relationship (SAR) studies pointed out their therapeutic utility and led to the discovery of promising drug candidates. Recently the cardiotonic steroid UNBS1450 01 (derived from 2-oxovoruscharin 02) from C. procera was shown to additionally exert an anti-cancer activity. UNBS1450 01 has been proven to be a potent sodium pump inhibitor, showing anti-proliferative and cell death-inducing activities. This anti-cancer potential of UNBS1450 01 is achieved by disorganization of the actin cytoskeleton after binding to the sodium pump at the cellular membrane, by inducing autophagy-related cell death, by repressing NF-kappaB activation as well as by down-regulating c-Myc in cancer cells. We aim to review pharmacologically important chemical extracts from C. procera and focus more specifically on the anti-cancer activities of UNBS1450 01.
机译:尽管在过去的几十年中肿瘤治疗学取得了重大进展,但是仍然渴望发现和开发新的,替代的或协同的抗癌药。几个世纪以来,人们已经知道粗灌木Calotropis procera是杀螨,裂殖,抗菌,驱虫,杀虫,消炎,抗腹泻,杀幼虫和细胞毒性化学物质的极有希望的来源。几个世纪以来,不同的化合物,如降冰片二烯酸酯,有机碳酸酯,半胱氨酸蛋白酶,半生物碱,类黄酮,固醇以及多种类型的烯醇内酯,为该植物提供了数百年的研究兴趣。心内酯的化学类别及其相关的生物活性评估和构效关系(SAR)研究指出了其治疗用途,并导致了有前途的候选药物的发现。最近,证明来自proc.procera的强心类固醇类固醇UNBS1450 01(衍生自2-氧代牛油精02)还具有抗癌活性。已证明UNBS1450 01是有效的钠泵抑制剂,显示出抗增殖和诱导细胞死亡的活性。 UNBS1450 01的这种抗癌潜能是通过在细胞膜上与钠泵结合后肌动蛋白细胞骨架紊乱,诱导自噬相关细胞死亡,抑制NF-κB活化以及下调c- Myc在癌细胞中。我们旨在审查proc。procera的重要药理学重要化学提取物,并更着重于UNBS1450 01的抗癌活性。

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