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首页> 外文期刊>Chemico-biological interactions >A natural piper-amide-like compound NED-135 exhibits a potent inhibitory effect on the invasive breast cancer cells
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A natural piper-amide-like compound NED-135 exhibits a potent inhibitory effect on the invasive breast cancer cells

机译:天然的类似哌啶的化合物NED-135对浸润性乳腺癌细胞具有有效的抑制作用

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Invasiveness and metastasis are the primary factors indicating poor prognosis in breast cancer patients. To identify a novel lead compound for the development of therapeutics for the treatment of breast cancer through inhibiting invasion, we screened the natural piper amide-like compounds library that we previously constructed. Among the compounds tested, (E)-3-(3,4-dimethoxyphenyI)-N-(4-hydroxyphenethyl)acrylamide (NED-135) showed potent inhibitory effects on matrix metalloproteinase (MMP)-9 and invasiveness of MCF10A human breast epithelial cells treated with an inflammatory lipid, sphingosine-1-phosphate (SIP). The invasive phenotypes of MDA-MB-231 and Hs578T triple-negative breast cancer cells were significantly inhibited by NED-135. NED-135 efficiently inhibited the SIP-induced MMP-9 expression at the transcriptional level with a comparable degree to FTY720, a known antagonist of SIP. We further showed that NED-135 significantly inhibited activation of SIP-induced signaling molecules, Akt, ERKs, and p38 MAPK. Computational similarity analysis led us to postulate that NED-135 and FTY720 may exert anti-invasive effects on breast cells possibly via different mechanisms. Due to its novel structural and functional features, we suggest that NED-135 can be used as a novel lead compound against breast cancer in an inflammatory microenvironment and highly invasive triple-negative breast cancer. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:浸润和转移是表明乳腺癌患者预后不良的主要因素。为了鉴定一种通过抑制侵袭来开发治疗乳腺癌的新疗法的先导化合物,我们筛选了先前构建的天然哌啶类化合物库。在测试的化合物中,(E)-3-(3,4-二甲氧基苯基)-N-(4-羟基苯乙基)丙烯酰胺(NED-135)对基质金属蛋白酶(MMP)-9和MCF10A人乳腺的侵袭性显示出有效的抑制作用炎症脂质-1-鞘氨醇(SIP)处理的上皮细胞。 NED-135显着抑制了MDA-MB-231和Hs578T三阴性乳腺癌细胞的侵袭性表型。 NED-135在转录水平上可以有效抑制SIP诱导的MMP-9表达,其程度与FIP720(一种已知的SIP拮抗剂)相当。我们进一步表明,NED-135显着抑制了SIP诱导的信号分子,Akt,ERK和p38 MAPK的激活。计算相似性分析使我们推测NED-135和FTY720可能通过不同的机制对乳腺细胞产生抗侵袭作用。由于其新颖的结构和功能特性,我们建议将NED-135用作炎症微环境和高浸润性三阴性乳腺癌中新型的抗乳腺癌先导化合物。 (C)2015 Elsevier Ireland Ltd.保留所有权利。

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