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二氢杨梅素通过激活 JNK/C-Jun 和 ERK/C-Fos 依赖的 AP-1 通路,减弱 H₂O₂ 介导的 MMP-7 表达,从而抑制 SW620 细胞侵袭。

Dimerumic acid inhibits SW620 cell invasion by attenuating H₂O₂-mediated MMP-7 expression via JNK/C-Jun and ERK/C-Fos activation in an AP-1-dependent manner.

机构信息

Department of Surgery, National Taiwan University Hospital, Taipei, Taiwan.

出版信息

Int J Biol Sci. 2011;7(6):869-80. doi: 10.7150/ijbs.7.869. Epub 2011 Jul 19.

DOI:10.7150/ijbs.7.869
PMID:21814482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3149281/
Abstract

Reactive oxygen species (ROS) such as hydrogen peroxide (H₂O₂) in the tumor microenvironment play important roles in tumor invasion and metastasis. Recently, ROS have been reported to cause a significant increase in the production and expression of matrix metalloproteinase (MMP)-7, which is closely correlated with metastatic colorectal cancer. The present study was undertaken to evaluate the scavenging activity of dimerumic acid (DMA) for H₂O₂ isolated from Monascus-fermented rice to investigate the inhibitory effects of DMA on the invasive potential of SW620 human colon cancer cells, and to explore the mechanisms underlying both these phenomena. Our results showed that increased MMP-7 expression due to H₂O₂ exposure was mediated by activation of mitogen-activated protein kinases (MAPKs) such as Jun N-terminal kinase (JNK), extracellular-regulated kinase (ERK), and p38 kinase. DMA pretreatment suppressed activation of H₂O₂-mediated MAPK pathways and cell invasion. Moreover, H₂O₂-triggered MMP-7 production was demonstrated via JNK/c-Jun and ERK/c-Fos activation in an activating protein 1 (AP-1)-dependent manner. Taken together, these results suggest that DMA suppresses H₂O₂-induced cell invasion by inhibiting AP-1-mediated MMP-7 gene transcription via the JNK/c-Jun and ERK/c-Fos signaling pathways in SW620 human colon cancer cells. Our data suggest that DMA may be useful in minimizing the development of colorectal metastasis. In the future, DMA supplementation may be a beneficial antioxidant to enhance surgical outcomes.

摘要

活性氧(ROS)如肿瘤微环境中的过氧化氢(H₂O₂)在肿瘤侵袭和转移中起重要作用。最近,ROS 被报道导致基质金属蛋白酶(MMP)-7 的产生和表达显著增加,这与转移性结直肠癌密切相关。本研究旨在评估红曲米发酵产物中二聚酸(DMA)对 H₂O₂的清除活性,以研究 DMA 对 SW620 人结肠癌细胞侵袭潜力的抑制作用,并探讨这两种现象的潜在机制。结果表明,H₂O₂暴露导致的 MMP-7 表达增加是通过丝裂原活化蛋白激酶(MAPK)如 Jun N-末端激酶(JNK)、细胞外调节激酶(ERK)和 p38 激酶的激活介导的。DMA 预处理抑制了 H₂O₂介导的 MAPK 通路的激活和细胞侵袭。此外,通过 JNK/c-Jun 和 ERK/c-Fos 的激活,H₂O₂触发的 MMP-7 产生是 AP-1 依赖性的。综上所述,这些结果表明,DMA 通过抑制 JNK/c-Jun 和 ERK/c-Fos 信号通路抑制 AP-1 介导的 MMP-7 基因转录,从而抑制 SW620 人结肠癌细胞中 H₂O₂诱导的细胞侵袭。我们的数据表明,DMA 可能有助于减少结直肠癌转移的发生。未来,DMA 补充剂可能是一种有益的抗氧化剂,可增强手术效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/831958667aef/ijbsv07p0869g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/81a52036e788/ijbsv07p0869g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/a740f7d4202d/ijbsv07p0869g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/354c43538eb1/ijbsv07p0869g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/6621ee28ce01/ijbsv07p0869g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/d6a01424290f/ijbsv07p0869g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/831958667aef/ijbsv07p0869g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/81a52036e788/ijbsv07p0869g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/a740f7d4202d/ijbsv07p0869g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/354c43538eb1/ijbsv07p0869g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/6621ee28ce01/ijbsv07p0869g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/d6a01424290f/ijbsv07p0869g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc6f/3149281/831958667aef/ijbsv07p0869g06.jpg

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