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首页> 外文期刊>Archives of pharmacal research >Ursolic acid-induced apoptosis in K562 cells involving upregulation of PTEN gene expression and inactivation of the PI3K/Akt pathway.
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Ursolic acid-induced apoptosis in K562 cells involving upregulation of PTEN gene expression and inactivation of the PI3K/Akt pathway.

机译:熊果酸诱导的K562细胞凋亡涉及PTEN基因表达的上调和PI3K / Akt途径的失活。

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摘要

Ursolic acid (UA), a pentacyclic triterpenoid derived from a variety of medicinal plants, exhibits potent anticancer activity against many types of cancer cells. However, the anticancer mechanism of UA is not clearly understood. Suppression of phosphatase and a tensin homolog deleted on chromosome 10 (PTEN) gene expression leading to activation of the phosphatidylinositol-3-OH kinase (PI3K)/Akt pathway has been observed in many cancers including leukemia, making the PTEN gene and PI3K/Akt pathway a central target for cancer therapy. Here, we demonstrated that UA was able to inhibit growth, induce apoptosis in a human chronic myelogenous leukemia cell line (K562 cells) via upregulation of PTEN gene expression, inhibit Akt kinase activity, change mitochondrial transmembrane potential and reduce the release of cytochrome c and the activity of caspases. These results suggest that UA may elicit its strong antitumor effects via upregulation of the PTEN gene and inhibition of the PI3K/Akt pathway.
机译:乌索酸(UA)是一种衍生自多种药用植物的五环三萜类化合物,对多种类型的癌细胞均表现出强大的抗癌活性。但是,UA的抗癌机制尚不清楚。在包括白血病在内的许多癌症中都观察到了磷酸酶的抑制和10号染色体(PTEN)基因表达上缺失的张力蛋白同源物的激活,导致磷脂酰肌醇-3-OH激酶(PI3K)/ Akt通路的激活,使得PTEN基因和PI3K / Akt通路是癌症治疗的主要目标。在这里,我们证明了UA能够通过上调PTEN基因表达,抑制Akt激酶活性,改变线粒体跨膜电位并减少细胞色素c和c的释放来抑制人类慢性粒细胞白血病细胞(K562细胞)的生长,诱导其凋亡。半胱氨酸蛋白酶的活性。这些结果表明,UA可能通过上调PTEN基因和抑制PI3K / Akt途径引起其强大的抗肿瘤作用。

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