首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Oncogenic microRNA-27a is a target for anticancer agent methyl 2-cyano-3,11-dioxo-18beta-olean-1,12-dien-30-oate in colon cancer cells.
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Oncogenic microRNA-27a is a target for anticancer agent methyl 2-cyano-3,11-dioxo-18beta-olean-1,12-dien-30-oate in colon cancer cells.

机译:致癌性microRNA-27a是结肠癌细胞中抗癌药2-cyano-3,11-dioxo-18beta-olean-1,12-dien-30-oate的靶标。

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摘要

Methyl 2-cyano-3,11-dioxo-18beta-olean-1,12-dien-30-oate (CDODA-Me) is a synthetic derivative of glycyrrhetinic acid, a triterpenoid phytochemical found in licorice extracts. CDODA-Me inhibited growth of RKO and SW480 colon cancer cells and this was accompanied by decreased expression of Sp1, Sp3 and Sp4 protein and mRNA and several Sp-dependent genes including survivin, vascular endothelial growth factor (VEGF), and VEGF receptor 1 (VEGFR1 or Flt-1). CDODA-Me also induced apoptosis, arrested RKO and SW480 cells at G(2)/M, and inhibited tumor growth in athymic nude mice bearing RKO cells as xenografts. CDODA-Me decreased expression of microRNA-27a (miR-27a), and this was accompanied by increased expression of 2 miR-27a-regulated mRNAs, namely ZBTB10 (an Sp repressor) and Myt-1 which catalyzes phosphorylation of cdc2 to inhibit progression of cells through G(2)/M. Both CDODA-Me and antisense miR-27a induced comparable responses in RKO and SW480 cells, suggesting that the potent anticarcinogenic activity of CDODA-Me is due to repression of oncogenic miR-27a.
机译:2-氰基-3,11-二氧杂-18beta-olean-1,12-dien-30-oate甲酯(CDODA-Me)是甘草次酸的一种合成衍生物,甘草提取物中发现了一种三萜类植物化学物质。 CDODA-Me抑制RKO和SW480结肠癌细胞的生长,并伴有Sp1,Sp3和Sp4蛋白和mRNA以及一些依赖于Sp的基因(包括生存素,血管内皮生长因子(VEGF)和VEGF受体1)的表达降低( VEGFR1或Flt-1)。 CDODA-Me还诱导凋亡,在G(2)/ M处逮捕RKO和SW480细胞,并抑制携带RKO细胞作为异种移植的无胸腺裸鼠的肿瘤生长。 CDODA-Me降低了microRNA-27a(miR-27a)的表达,并伴有2个miR-27a调控的mRNA表达的增加,即ZBTB10(Sp阻遏物)和Myt-1,它们催化cdc2的磷酸化以抑制进展。通过G(2)/ M的细胞数。 CDODA-Me和反义miR-27a均可在RKO和SW480细胞中诱导可比的应答,这表明CDODA-Me的有效抗癌活性是由于抑制致癌miR-27a。

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