Ke Zunji, Lin Hong, Fan Zhiqin, Cai Tian-Quan, Kaplan Rebecca A, Ma Cuiling, Bower Kimberly A, Shi Xianglin, Luo Jia
Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, People's Republic of China.
Int J Cancer. 2006 Jul 1;119(1):8-16. doi: 10.1002/ijc.21769.
Ethanol is a tumor promoter and may enhance the metastasis of breast cancer. We have previously demonstrated that over-expression of ErbB2 promoted ethanol-mediated invasion of mammary epithelial cells and breast cancer cells. However, the underlying cellular/molecular mechanisms remain unknown. By gelatin zymography, we showed that over-expression of ErbB2 increased the production of matrix metalloproteinase-2 (MMP-2) and MMP-9 in human mammary epithelial cells (HB2). Transient or stable transfection of ErbB2 cDNA to HB2 cells upregulated the transcripts and the activity of the MMP-2/-9 gene promoter; the upregulation of MMP-2/-9 expression was mediated by p38 mitogen-activated protein kinase (p38 MAPK) and phosphatidylinositol 3-kinase (PI3K). Although ethanol, at physiologically relevant concentrations (100-400 mg/dl), did not affect the production of MMP-2/-9, it activated MMP-2 in HB2 cells over-expressing ErbB2 (HB2(ErbB2)), but not HB2 cells; it enhanced the cleavage of proform MMP-2 (72 kDa) to an active form (62 kDa). The activation was dependent on c-jun N-terminal kinases (JNKs) and reactive oxygen species (ROS). On the other hand, ethanol affected neither the expression nor the activation of MMP-9. Selective inhibitors of MMP-2 (SB-3CT and OA-Hy) and antioxidants significantly inhibited ethanol-stimulated invasion of HB2(ErbB2) cells. Furthermore, knocking down MMP-2 by small interference RNA also induced a partial blockage on ethanol-promoted invasion of HB2(ErbB2) cells. Thus, ethanol-stimulated invasion of cells over-expressing ErbB2 was mediated, at least partially, by MMP-2 activation.
乙醇是一种肿瘤促进剂,可能会增强乳腺癌的转移。我们之前已经证明,ErbB2的过表达促进了乙醇介导的乳腺上皮细胞和乳腺癌细胞的侵袭。然而,潜在的细胞/分子机制仍然未知。通过明胶酶谱法,我们发现ErbB2的过表达增加了人乳腺上皮细胞(HB2)中基质金属蛋白酶-2(MMP-2)和MMP-9的产生。将ErbB2 cDNA瞬时或稳定转染到HB2细胞中可上调MMP-2/-9基因启动子的转录本和活性;MMP-2/-9表达的上调由p38丝裂原活化蛋白激酶(p38 MAPK)和磷脂酰肌醇3-激酶(PI3K)介导。虽然在生理相关浓度(100 - 400 mg/dl)下,乙醇不影响MMP-2/-9的产生,但它能激活过表达ErbB2的HB2细胞(HB2(ErbB2))中的MMP-2,而不影响HB2细胞;它增强了前体MMP-2(72 kDa)向活性形式(62 kDa)的切割。这种激活依赖于c-jun氨基末端激酶(JNKs)和活性氧(ROS)。另一方面,乙醇既不影响MMP-9的表达也不影响其激活。MMP-2的选择性抑制剂(SB-3CT和OA-Hy)和抗氧化剂显著抑制了乙醇刺激的HB2(ErbB2)细胞的侵袭。此外,通过小干扰RNA敲低MMP-2也部分阻断了乙醇促进的HB2(ErbB2)细胞的侵袭。因此,乙醇刺激的过表达ErbB2细胞的侵袭至少部分是由MMP-2激活介导的。