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Inhibition of Invasion in Pancreatic Cancer Cells by Conjugate of EPA with beta(3,3)-Pip-OH via PI3K/Akt/NF-kB Pathway

机译:通过PI3K / Akt / NF-kB途径与β(3,3)-Pip-OH缀合EPA抑制胰腺癌细胞的侵袭

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摘要

The present work describes the anti-invasive effect of conjugate BC06, a novel conjugate of EPA, (2E,4E)-4-(benzo[d][1,3]dioxol-5-ylmethylene) hex-2-enoic acid with beta,beta-disubstituted-beta-amino acid, beta(3,3)-Pip-OH (2-(4-aminopiperidin-4-yl)acetic acid), in human pancreatic carcinoma. The conjugate BC06 inhibited invasion and migration of PANC-1 cells in wound healing, matrigel invasion, and gelatin degradation assays. Apart from suppressing PI3K/Akt/NF-kB signaling, which is involved in the up-regulation of matrix metalloproteinases, our study also demonstrated that dose-dependent treatment of BC06 results in the upregulation of TIMP-I and E-cadherin expression. Further, BC06 was found to be inhibiting the metastatic ability of PANC-1 cells by reducing MMP-2 and MMP-9 expression. These findings suggest that EPA conjugate with beta(3,3)-Pip-OH, BC06, may be used as an anti-invasive agent against human pancreatic carcinoma.
机译:本工作描述了一种新型的EPA缀合物BC06缀合物BC06(2E,4E)-4-(苯并[d] [1,3]二恶酚-5-基亚甲基)己-2-烯酸的抗侵袭作用β,β-二取代的β-氨基酸,β(3,3)-Pip-OH(2-(4-氨基哌啶-4-基)乙酸),在人类胰腺癌中。在伤口愈合,基质胶侵袭和明胶降解试验中,缀合物BC06抑制了PANC-1细胞的侵袭和迁移。除了抑制PI3K / Akt / NF-kB信号传导(涉及基质金属蛋白酶的上调)外,我们的研究还证明剂量依赖性治疗BC06会导致TIMP-1和E-钙黏着蛋白表达上调。此外,发现BC06通过降低MMP-2和MMP-9表达来抑制PANC-1细胞的转移能力。这些发现表明,EPA与β(3,3)-Pip-OH,BC06的共轭物可用作抗人胰腺癌的抗侵袭剂。

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