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来自 Orostachys japonicus A. Berger 的类黄酮通过使 Akt 失活和调节紧密连接来抑制 LnCaP 前列腺癌细胞的侵袭。

Flavonoids from Orostachys japonicus A. Berger inhibit the invasion of LnCaP prostate carcinoma cells by inactivating Akt and modulating tight junctions.

机构信息

Dongnam Institute of Radiological & Medicine Sciences, Busan 619-953, Korea.

出版信息

Int J Mol Sci. 2013 Sep 6;14(9):18407-20. doi: 10.3390/ijms140918407.

Abstract

Tight junctions (TJs) are a mode of cell-to-cell adhesion in epithelial or endothelial cells, and serve as a physical barrier to maintenance of homeostasis in body by controlling paracellular transport. Claudins are the most important molecules of the TJs, but paradoxically these proteins are frequently over-expressed in cancers and their overexpression is implicated in the invasive potential of cancer. Hence, we investigated the effects of flavonoids extracted from Orostachys japonicus A. Berger (FEOJ) on TJs and the expression of claudins as well as cancer invasion along with in LnCaP human prostate cancer. FEOJ suppressed cancer cell motility and invasiveness at the concentrations where FEOJ did not show anti-proliferative activity. FEOJ increased transepithelial electrical resistance (TER) associated with tightening TJs, and suppressed expression of claudin proteins. Furthermore, FEOJ suppressed the activities of MMP-2 and -9 in a dose-dependent manner, which came from the activation of tissue inhibitor of metalloproteinases (TIMPs) by FEOJ. FEOJ suppressed migration and invasion by suppressing PI3K/Akt signaling pathway. Taken together, this study suggest that FEOJ suppresses cancer migration and invasion by tightening TJs through the suppression of claudin expression, and by suppressing MMPs in LnCaP human prostate cancer cells, which at least in part results from the suppression of PI3K/Akt signaling pathway.

摘要

紧密连接(TJs)是上皮或内皮细胞中细胞间黏附的一种方式,通过控制细胞旁通透性,作为维持体内内稳态的物理屏障。紧密连接蛋白是 TJ 的最重要分子,但矛盾的是,这些蛋白质在癌症中经常过度表达,其过度表达与癌症的侵袭潜力有关。因此,我们研究了来自 Orostachys japonicus A. Berger(FEOJ)的类黄酮对 TJ 和 Claudin 表达以及前列腺癌 LnCaP 人前列腺癌细胞侵袭的影响。FEOJ 在不显示抗增殖活性的浓度下抑制癌细胞的迁移和侵袭。FEOJ 增加了与 TJ 收紧相关的跨上皮电阻(TER),并抑制了 Claudin 蛋白的表达。此外,FEOJ 以剂量依赖的方式抑制 MMP-2 和 MMP-9 的活性,这是由 FEOJ 激活金属蛋白酶组织抑制剂(TIMPs)所致。FEOJ 通过抑制 PI3K/Akt 信号通路来抑制迁移和侵袭。综上所述,本研究表明,FEOJ 通过抑制 Claudin 表达和抑制 LnCaP 人前列腺癌细胞中的 MMPs 来抑制肿瘤细胞的迁移和侵袭,至少部分是通过抑制 PI3K/Akt 信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed1d/3794786/96a8b976bebc/ijms-14-18407f1.jpg

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