Cao Lei, Liu Jiangbo, Zhang Lun, Xiao Xue, Li Wei
Department of Pharmacology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi 710061, P.R. China.
Department of Hepatobiliary Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China.
Oncol Rep. 2016 Oct;36(4):2245-51. doi: 10.3892/or.2016.5044. Epub 2016 Aug 25.
Curcumin (diferuloylmethane), a natural polyphenol present in turmeric, possesses a wide spectrum of pharmacological properties, including antioxidant and antitumor metastatic activities. However, the underlying mechanisms by which curcumin suppresses the metastasis of pancreatic cancer are still not fully elucidated. Our previous study demonstrated that a moderate amount of hydrogen peroxide (H2O2) is able to promote pancreatic cancer invasion. The aim of this study was to determine whether curcumin can suppress H2O2-induced tumor invasive and migratory abilities. Human pancreatic cancer BxPC-3 and Panc-1 cells were exposed to H2O2 with or without curcumin or N-acetylcysteine (NAC; a scavenger of free radicals). The effects of curcumin on pancreatic cancer cell proliferation was analyzed using MTT assay. The intracellular reactive oxygen species (ROS) was determined using 2,7-dichlorodihydrofluorecein diacetate. The cellular invasive and migratory abilities were analyzed using Transwell Matrigel invasion assay and wound healing assay, respectively. The expressions of matrix metalloproteinase (MMP)-2 and MMP-9 were determined using qT-PCR and western blotting at mRNA and protein level. The activation of p-extracellular signal-regulated kinase (ERK) and p-nuclear factor-κB (NF-κB) were measured by western blotting. Our data showed that curcumin inhibited cancer cell proliferation in a dose-dependent manner. Curcumin and NAC were able to inhibit H2O2-induced ROS production, reduce the migration and invasion, and decrease the expression of MMP-2 and MMP-9 in pancreatic cancer cells. In addition, the H2O2‑induced elevation of p-ERK and p-NF-κB in BxPC-3 and Panc-1 cells were reduced by curcumin, NAC and PD 98059 (an ERK inhibitor). These data indicate that curcumin suppresses pancreatic cancer migration and invasion through the inhibition of the ROS/ERK/NF-κB signaling pathway. This study suggests that curcumin may be a potential anticancer agent for pancreatic cancer.
姜黄素(二阿魏酰甲烷)是姜黄中存在的一种天然多酚,具有广泛的药理特性,包括抗氧化和抗肿瘤转移活性。然而,姜黄素抑制胰腺癌转移的潜在机制仍未完全阐明。我们之前的研究表明,适量的过氧化氢(H2O2)能够促进胰腺癌侵袭。本研究的目的是确定姜黄素是否能抑制H2O2诱导的肿瘤侵袭和迁移能力。将人胰腺癌BxPC-3和Panc-1细胞暴露于有或无姜黄素或N-乙酰半胱氨酸(NAC;一种自由基清除剂)的H2O2中。使用MTT法分析姜黄素对胰腺癌细胞增殖的影响。使用2,7-二氯二氢荧光素二乙酸酯测定细胞内活性氧(ROS)。分别使用Transwell Matrigel侵袭试验和伤口愈合试验分析细胞的侵袭和迁移能力。使用qT-PCR和蛋白质印迹法在mRNA和蛋白质水平测定基质金属蛋白酶(MMP)-2和MMP-9的表达。通过蛋白质印迹法检测p-细胞外信号调节激酶(ERK)和p-核因子-κB(NF-κB)的激活情况。我们的数据表明,姜黄素以剂量依赖的方式抑制癌细胞增殖。姜黄素和NAC能够抑制H2O2诱导的ROS产生,减少迁移和侵袭,并降低胰腺癌细胞中MMP-2和MMP-9的表达。此外,姜黄素、NAC和PD 98059(一种ERK抑制剂)降低了H2O2诱导的BxPC-3和Panc-1细胞中p-ERK和p-NF-κB的升高。这些数据表明,姜黄素通过抑制ROS/ERK/NF-κB信号通路抑制胰腺癌的迁移和侵袭。本研究表明,姜黄素可能是一种潜在的胰腺癌抗癌药物。