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Cytotoxicity of triterpenoids-enriched extracts from bark of Eucalyptus nitens against colorectal HCT116 cancer cells

机译:桉树树皮中富含三萜类成分的提取物对结直肠癌HCT116癌细胞的细胞毒性

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摘要

Eucalyptus nitens crops are used in Portugal mainly by the pulp and paper industries, producing substantial bark residues with no added value use [1]. They can, however, be an interesting source of bioactive triterpenic compounds. Here, a lipophilic crude extract (CE) from bark of E. nitens prepared with dichloromethane [1] with about 70% (w/w) of triterpenoids, and a fraction of this (F2) more enriched in triterpenoids (93% w/w), as well as their main compounds betulinic acid (BiA) and betulonic acid (BoA), were used to determine their potential cytotoxicity against the colorectal HCT116 cancer cells. After 48h of incubation, the extracts/compounds inhibited significantly cell growth in a concentration-dependent manner (assessed by the MTT assay), with a GI50 s of 1.3 µg/mL and 2.2 µg/mL for F2 and CE extracts, respectively, and of 0.8µM and 3.9µM for BoA and BiA, respectively. The inhibition of cell growth was shown to be dependent on both the arrest of cell cycle at the G2/M phase, and the induction of cell death (assessed by PI staining). At the higher concentrations tested (up to 25µM), apoptosis was the major contributor to the observed cell death, and that was associated with JNK activation. Using the JNK inhibitor SP600125 and the pan-caspase inhibitor z-VAD, apoptosis induced by the extracts/compounds was shown to be dependent on JNK and caspases activation. At intermediate concentrations of extracts/compounds, a delayed and non-apoptotic type of cell death was present, which was associated with a significant activation of AMPK and a decrease of p53 levels. Altogether, these results demonstrate that the wasted bark of E. nitens can be used as a potential source of interesting cytotoxic natural triterpenoids against cancer cells.
机译:在葡萄牙,桉树农作物主要用于制浆和造纸工业,产生大量树皮残留物,无附加值[1]。但是,它们可能是生物活性三萜化合物的有趣来源。在这里,用二氯甲烷[1]和约70%(w / w)的三萜类化合物制备了一种从大肠埃希菌的树皮中提取的亲脂性粗提物(CE),其中一部分(F2)富含三萜类化合物(93%w / w w)及其主要化合物桦木酸(BiA)和桦木酸(BoA)用于确定其对结直肠HCT116癌细胞的潜在细胞毒性。孵育48小时后,提取物/化合物以浓度依赖性方式显着抑制细胞生长(通过MTT分析评估),F2和CE提取物的GI50分别为1.3 µg / mL和2.2 µg / mL。 BoA和BiA分别为0.8µM和3.9µM。已显示细胞生长的抑制依赖于细胞周期在G2 / M期的停滞和细胞死亡的诱导(通过PI染色评估)。在较高的测试浓度下(最高25µM),凋亡是导致观察到的细胞死亡的主要因素,并且与JNK活化有关。使用JNK抑制剂SP600125和泛半胱天冬酶抑制剂z-VAD,提取物/化合物诱导的凋亡显示出依赖于JNK和胱天蛋白酶的活化。在提取物/化合物的中间浓度下,存在延迟和非凋亡类型的细胞死亡,这与AMPK的显着激活和p53水平的降低有关。总而言之,这些结果表明,浪费的大肠埃希氏菌的树皮可以用作潜在的有趣的针对癌细胞的细胞毒性天然三萜类化合物。

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