Hwang Jin-Ki, Yu Hong-Nu, Noh Eun-Mi, Kim Jeong-Mi, Hong On-Yu, Youn Hyun Jo, Jung Sung Hoo, Kwon Kang-Beom, Kim Jong-Suk, Lee Young-Rae
Center for Metabolic Function Regulation, Wonkwang University School of Medicine, Iksan, Jeonbuk 570-749, Republic of Korea.
Department of Oncology Medicine, Xinhua Hospital Affiliated to Dalian University, Dalian, Liaoning 116021, P.R. China.
Oncol Lett. 2017 Jan;13(1):243-249. doi: 10.3892/ol.2016.5382. Epub 2016 Nov 11.
Docosahexaenoic acid (DHA) is an omega-3 fatty acid that is considered to have applications in cancer prevention and treatment. The beneficial effects of DHA against cancer metastasis are well established; however, the mechanisms underlying these effects in breast cancer are not clear. Cell invasion is critical for neoplastic metastasis, and involves the degradation of the extracellular matrix by matrix metalloproteinase (MMP)-9. The present study investigated the inhibitory effect of DHA on MMP-9 expression and cell invasion induced by 12--tetradecanoylphorbol-13-acetate (TPA) in the MCF-7 breast cancer cell line. DHA inhibited the TPA-induced activation of mitogen-activated protein kinase (MAPK) and the transcription of nuclear factor (NF)-κB, but did not inhibit the transcription of activator protein-1. DHA increased the activity of peroxisome proliferator-activated receptor (PPAR)-γ, an effect that was reversed by the application of the PPAR-γ antagonist GW9662. In addition, combined treatment with GW9662 and DHA increased NF-κB-related protein expression. These results indicate that DHA regulates MMP-9 expression and cell invasion via modulation of the MAPK signaling pathway and PPAR-γ/NF-κB activity. This suggests that DHA could be a potential therapeutic agent for the prevention of breast cancer metastasis.
二十二碳六烯酸(DHA)是一种ω-3脂肪酸,被认为在癌症预防和治疗方面具有应用价值。DHA对癌症转移的有益作用已得到充分证实;然而,其在乳腺癌中发挥这些作用的机制尚不清楚。细胞侵袭对于肿瘤转移至关重要,且涉及基质金属蛋白酶(MMP)-9对细胞外基质的降解。本研究调查了DHA对MCF-7乳腺癌细胞系中由12-十四酰佛波醇-13-乙酸酯(TPA)诱导的MMP-9表达和细胞侵袭的抑制作用。DHA抑制了TPA诱导的丝裂原活化蛋白激酶(MAPK)激活和核因子(NF)-κB的转录,但未抑制活化蛋白-1的转录。DHA增加了过氧化物酶体增殖物激活受体(PPAR)-γ的活性,应用PPAR-γ拮抗剂GW9662可逆转这一效应。此外,GW9662与DHA联合处理增加了NF-κB相关蛋白的表达。这些结果表明,DHA通过调节MAPK信号通路以及PPAR-γ/NF-κB活性来调控MMP-9表达和细胞侵袭。这表明DHA可能是预防乳腺癌转移的一种潜在治疗药物。