Ferlazzo Nadia, Cirmi Santa, Russo Marina, Trapasso Elena, Ursino Maria Rita, Lombardo Giovanni Enrico, Gangemi Sebastiano, Calapai Gioacchino, Navarra Michele
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy.
Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy; Institute of Applied Sciences and Intelligent Systems, ISASI CNR, Messina, Italy.
Life Sci. 2016 Feb 1;146:81-91. doi: 10.1016/j.lfs.2015.12.040. Epub 2016 Jan 5.
Among cancers, hepatocellular carcinoma is one of the commonest worldwide, and its incidence is increasing around the world. A lot of evidence underlines that natural substances usually consumed in the diet can have an important role in the prevention of cancer. In this study we investigated the molecular mechanisms underlying the antiproliferative activity of Citrus bergamia (bergamot) juice (BJ) in human hepatocellular carcinoma HepG2 cells.
HepG2 cells were exposed to BJ and then cell proliferation, cell cycle progression, apoptosis and NF-κB nuclear translocation were evaluated.
Here we present results demonstrating that BJ reduced the growth rate of human hepatocellular carcinoma HepG2 cells in a time- and concentration-dependent manner, by a mechanism involving the activation of apoptotic machinery via both intrinsic and extrinsic pathways. Moreover, BJ increased expression of P53 and P21 proteins that may be responsible for the HepG2 cell cycle arrest in G2 phase. In addition, BJ reduced NF-κB nuclear translocation.
Our data demonstrate the ability of BJ in reducing the growth of HepG2 cells, revealing its mechanism of action and suggesting a promising role as anticancer drugs.
在各类癌症中,肝细胞癌是全球最常见的癌症之一,且其发病率在全球范围内呈上升趋势。大量证据表明,日常饮食中常见的天然物质在癌症预防中可发挥重要作用。在本研究中,我们探究了香柠檬(佛手柑)汁(BJ)对人肝癌HepG2细胞抗增殖活性的分子机制。
将HepG2细胞暴露于BJ中,然后评估细胞增殖、细胞周期进程、细胞凋亡和核因子κB(NF-κB)核转位情况。
我们在此展示的结果表明,BJ以时间和浓度依赖性方式降低人肝癌HepG2细胞的生长速率,其机制涉及通过内在和外在途径激活凋亡机制。此外,BJ增加了P53和P21蛋白的表达,这可能是导致HepG2细胞周期阻滞于G2期的原因。此外,BJ减少了NF-κB核转位。
我们的数据证明了BJ具有降低HepG2细胞生长的能力,揭示了其作用机制,并表明其作为抗癌药物具有广阔前景。