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首页> 外文期刊>Journal of pharmacological sciences. >The Cadin-2-en-1β-ol-1β-D-glucuronopyranoside suppresses TPA-mediated matrix metalloproteinase-9 expression through the ERK signaling pathway in MCF-7 human breast adenocarcinoma cells
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The Cadin-2-en-1β-ol-1β-D-glucuronopyranoside suppresses TPA-mediated matrix metalloproteinase-9 expression through the ERK signaling pathway in MCF-7 human breast adenocarcinoma cells

机译:Cadin-2-en-1β-ol-1β-D-葡萄糖醛酸吡喃糖苷通过ERK信号通路抑制TPA介导的基质金属蛋白酶9在MCF-7人乳腺癌细胞中的表达。

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摘要

A sesquiterpene glycoside, cadin-2-en-1β-ol-1β-D- glucuronopyranoside (known as CR4-1), was isolated from Catharanthus roseus (Apocynaceae) hairy root cultures. C. roseus is widely used as an ornamental and medicinal plant and is cultivated mainly for its alkaloids. C. roseus has been reported to have pharmacologic properties such as anti-cancer, enzymatic anti-oxidant, and anti-diabetic effects. In this study, we demonstrated that CR4-1 significantly inhibited the in vitro invasion of MCF-7 human breast adenocarcinoma cells induced by 12-O-tetradecanoyl phorbol-13-acetate (TPA). Matrix metalloproteinases (MMPs) are known to be involved in cancer invasion and metastasis. Zymographic analysis showed that CR4-1 suppressed TPA-induced MMP-9 activity in a dose-dependent manner. We further demonstrated that CR4-1 suppressed the phosphorylation of extracellular signal-regulated protein kinase, but not p38 kinase or c-Jun N-terminal kinase (JNK). Moreover, CR4-1 attenuated TPA-induced degradation of κBα inhibitor (IκB-α). These results suggest that CR4-1 reduces the invasiveness of human cancer cells by suppressing MMP-9 expression through inhibition of the NF-κB signaling pathways.
机译:从长春花(Apocynaceae)毛状根培养物中分离出倍半萜糖苷,cadin-2-en-1β-ol-1β-D-葡糖醛酸吡喃糖苷(称为CR4-1)。玫瑰果念珠菌被广泛用作观赏和药用植物,主要​​由于其生物碱而被种植。据报道玫瑰色梭菌具有药理性质,例如抗癌,酶促抗氧化剂和抗糖尿病作用。在这项研究中,我们证明了CR4-1可以显着抑制12-O-十四烷酰佛波醇13-乙酸酯(TPA)诱导的MCF-7人乳腺腺癌细胞的体外侵袭。基质金属蛋白酶(MMP)已知与癌症的侵袭和转移有关。谱线分析显示CR4-1以剂量依赖性方式抑制TPA诱导的MMP-9活性。我们进一步证明,CR4-1抑制细胞外信号调节蛋白激酶的磷酸化,但不抑制p38激酶或c-Jun N端激酶(JNK)的磷酸化。此外,CR4-1减弱了TPA诱导的κBα抑制剂(IκB-α)的降解。这些结果表明CR4-1通过抑制NF-κB信号传导途径抑制MMP-9表达而降低了人类癌细胞的侵袭性。

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