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民族药物菝葜的甲醇提取物具有抗肿瘤活性。

Methanol extract of the ethnopharmaceutical remedy Smilax spinosa exhibits anti-neoplastic activity.

机构信息

Institute of Clinical Pathology, Medical University of Vienna, Vienna, Austria.

出版信息

Int J Oncol. 2012 Sep;41(3):1164-72. doi: 10.3892/ijo.2012.1538. Epub 2012 Jun 29.

Abstract

Plants have been the source of several effective drugs for the treatment of cancer and over 60% of anticancer drugs originate from natural sources. Therefore, extracts of the rhizome of Smilax spinosa, an ethnomedicinal plant from Guatemala which is used for the treatment of inflammatory conditions, were investigated regarding their anti-neoplastic activities. By using several solvents the methanol extract was by far the most potent against HL60 cell proliferation (50% inhibition at 60 µg/ml). Furthermore, fractionation of this extract yielded fraction F2, which exhibited enforced pro-apoptotic activity, and activated CYP1A1. Proteins that are relevant for cell cycle progression and apoptosis, as well as proto-oncogenes were investigated by western blotting. This revealed that the methanol extract increased the levels of p21 and this may have caused cell cycle attenuation. The derivative fraction F2 induced apoptosis through the intrinsic pathway, which correlated with the inhibition of Stat3 phosphorylation and concomitant induction of caspase 9, then caspase 8 and caspase 3. In summary, the methanol extract and the derivative fraction F2 of S. spinosa showed anti-neoplastic effects in HL-60 cells and CYP1A1 activation in estrogen receptor-positive MCF-7 breast cancer cells but not in estrogen-negative MDA-MB231 breast cancer cells. Based on our data Smilax spinosa may be a promising source for novel anticancer agents.

摘要

植物一直是治疗癌症的几种有效药物的来源,超过 60%的抗癌药物源自天然来源。因此,研究了来自危地马拉的民族药用植物菝葜根茎的提取物,因为它被用于治疗炎症性疾病,以研究其抗肿瘤活性。通过使用几种溶剂,甲醇提取物的抗肿瘤活性最强(在 60μg/ml 时对 HL60 细胞增殖的 50%抑制作用)。此外,对该提取物进行的分级分离得到了具有增强促凋亡活性的 F2 级分,并激活了 CYP1A1。通过 Western blot 研究了与细胞周期进展和细胞凋亡相关的蛋白质以及原癌基因。这表明甲醇提取物增加了 p21 的水平,这可能导致细胞周期衰减。衍生的 F2 级分通过内在途径诱导细胞凋亡,这与 Stat3 磷酸化的抑制以及伴随的半胱天冬酶 9、半胱天冬酶 8 和半胱天冬酶 3 的诱导相关。总之,菝葜的甲醇提取物和衍生的 F2 级分在 HL-60 细胞中表现出抗肿瘤作用,并在雌激素受体阳性 MCF-7 乳腺癌细胞中激活 CYP1A1,但在雌激素阴性 MDA-MB231 乳腺癌细胞中没有。基于我们的数据,菝葜可能是一种有前途的新型抗癌药物来源。

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