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Isolation Characterization and Anticancer Potential of Cytotoxic Triterpenes from Betula utilis Bark

机译:桦木皮细胞毒性三萜的分离鉴定及抗癌潜力

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摘要

Betula utilis, also known as Himalayan silver birch has been used as a traditional medicine for many health ailments like inflammatation, HIV, renal and bladder disorders as well as many cancers from ages. Here, we performed bio-guided fractionation of Betula utilis Bark (BUB), in which it was extracted in methanol and fractionated with hexane, ethyl acetate, chloroform, n-butanol and water. All six fractions were evaluated for their in-vitro anticancer activity in nine different cancer cell lines and ethyl acetate fraction was found to be one of the most potent fractions in terms of inducing cytotoxic activity against various cancer cell lines. By utilizing column chromatography, six triterpenes namely betulin, betulinic acid, lupeol, ursolic acid (UA), oleanolic acid and β-amyrin have been isolated from the ethyl acetate extract of BUB and structures of these compounds were unraveled by spectroscopic methods. β-amyrin and UA were isolated for the first time from Betula utilis. Isolated triterpenes were tested for in-vitro cytotoxic activity against six different cancer cell lines where UA was found to be selective for breast cancer cells over non-tumorigenic breast epithelial cells (MCF 10A). Tumor cell selective apoptotic action of UA was mainly attributed due to the activation of extrinsic apoptosis pathway via up regulation of DR4, DR5 and PARP cleavage in MCF-7 cells over non-tumorigenic MCF-10A cells. Moreover, UA mediated intracellular ROS generation and mitochondrial membrane potential disruption also play a key role for its anti cancer effect. UA also inhibits breast cancer migration. Altogether, we discovered novel source of UA having potent tumor cell specific cytotoxic property, indicating its therapeutic potential against breast cancer.
机译:桦木桦(Betula utilis)也被称为喜马拉雅白桦树,已被用作许多健康疾病的传统药物,例如炎症,HIV,肾和膀胱疾病以及许多年龄的癌症。在这里,我们进行了Betula utilis树皮(BUB)的生物引导分馏,其中将其提取于甲醇中,并用己烷,乙酸乙酯,氯仿,正丁醇和水进行分馏。评估了所有六种级分在九种不同癌细胞系中的体外抗癌活性,并且就诱导针对各种癌细胞系的细胞毒性活性而言,乙酸乙酯级分被认为是最有效的级分之一。利用柱色谱法,从BUB的乙酸乙酯提取物中分离出了六种三萜,即桦木素,桦木酸,羽扇豆醇,熊果酸(UA),齐墩果酸和β-糊精,并且通过光谱方法解开了这些化合物的结构。首次从Betula utilis中分离出β-amyrin和UA。测试了分离的三萜对六种不同癌细胞系的体外细胞毒活性,其中发现UA比非致瘤性乳腺上皮细胞(MCF 10A)对乳腺癌细胞具有选择性。 UA的肿瘤细胞选择性凋亡作用主要归因于外源性凋亡途径的激活,这是通过上调DR4,DR5和PARP在MCF-7细胞中的裂解而不是通过非致瘤性MCF-10A细胞来实现的。此外,UA介导的细胞内ROS生成和线粒体膜电位破坏也对其抗癌作用起着关键作用。 UA还抑制乳腺癌的迁移。总而言之,我们发现了具有有效的肿瘤细胞特异性细胞毒性特性的UA的新来源,表明其抗乳腺癌的治疗潜力。

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