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LFG-500通过下调PI3K/AKT/NF-κB信号通路抑制癌细胞的侵袭。

LFG-500 inhibits the invasion of cancer cells via down-regulation of PI3K/AKT/NF-κB signaling pathway.

作者信息

Li Chenglin, Li Fanni, Zhao Kai, Yao Jing, Cheng Yao, Zhao Li, Li Zhiyu, Lu Na, Guo Qinglong

机构信息

State Key Laboratory of Natural Medicines, Jiangsu Key Laboratory of Carcinogenesis and Intervention, Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, China Pharmaceutical University, Nanjing, People's Republic of China.

出版信息

PLoS One. 2014 Mar 11;9(3):e91332. doi: 10.1371/journal.pone.0091332. eCollection 2014.

Abstract

Cancer cell invasion, one of the crucial events in local growth and metastatic spread of tumors, possess a broad spectrum of mechanisms, especially altered expression of matrix metalloproteinases. LFG-500 is a novel synthesized flavonoid with strong anti-cancer activity, whose exact molecular mechanism remains incompletely understood. This current study was designed to examine the effects of LFG-500 on tumor metastasis using in vitro and in vivo assays. LFG-500 could inhibit adhesion, migration and invasion of MDA-MB-231 human breast carcinoma cells. Meanwhile, it reduced the activities and expression of MMP-2 and MMP-9 via suppressing the transcriptional activation of NF-κB rather than AP-1 or STAT3. Moreover, LFG-500 repressed TNF-α induced cell invasion through inhibiting NF-κB and subsequent MMP-9 activity. Further elucidation of the mechanism revealed that PI3K/AKT but not MAPK signaling pathway was involved in the inhibitory effect of LFG-500 on NF-κB activation. LFG-500 could also suppress lung metastasis of B16F10 murine melanoma cells in vivo. Taken together, these results demonstrated that LFG-500 could block cancer cell invasion via down-regulation of PI3K/AKT/NF-κB signaling pathway, which provides new evidence for the anti-cancer activity of LFG-500.

摘要

癌细胞侵袭是肿瘤局部生长和转移扩散的关键事件之一,具有广泛的机制,尤其是基质金属蛋白酶表达的改变。LFG - 500是一种具有强大抗癌活性的新型合成黄酮类化合物,其确切的分子机制仍未完全清楚。本研究旨在通过体外和体内实验检测LFG - 500对肿瘤转移的影响。LFG - 500可抑制MDA - MB - 231人乳腺癌细胞的黏附、迁移和侵袭。同时,它通过抑制NF - κB而非AP - 1或STAT3的转录激活来降低MMP - 2和MMP - 9的活性。此外,LFG - 500通过抑制NF - κB及随后的MMP - 9活性来抑制TNF - α诱导的细胞侵袭。对机制的进一步阐明表明,PI3K/AKT信号通路而非MAPK信号通路参与了LFG - 500对NF - κB激活的抑制作用。LFG - 500在体内也可抑制B16F10小鼠黑色素瘤细胞的肺转移。综上所述,这些结果表明LFG - 500可通过下调PI3K/AKT/NF - κB信号通路来阻断癌细胞侵袭,这为LFG - 500的抗癌活性提供了新证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba69/3950212/f20f67a5b158/pone.0091332.g001.jpg

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