MacDonald Gwen, Nalvarte Ivan, Smirnova Tatiana, Vecchi Manuela, Aceto Nicola, Dolemeyer Arno, Frei Anna, Lienhard Susanne, Wyckoff Jeffrey, Hess Daniel, Seebacher Jan, Keusch Jeremy J, Gut Heinz, Salaun Daniele, Mazzarol Giovanni, Disalvatore Davide, Bentires-Alj Mohamed, Di Fiore Pier Paolo, Badache Ali, Hynes Nancy E
Friedrich Miescher Institute for Biomedical Research, Basel 4058, Switzerland.
IFOM, Fondazione Istituto FIRC di Oncologia Molecolare, Milan 20139, Italy. Molecular Medicine Program, Department of Experimental Oncology, European Institute of Oncology, Milan 20141, Italy.
Sci Signal. 2014 Jun 10;7(329):ra56. doi: 10.1126/scisignal.2004870.
Memo is an evolutionarily conserved protein with a critical role in cell motility. We found that Memo was required for migration and invasion of breast cancer cells in vitro and spontaneous lung metastasis from breast cancer cell xenografts in vivo. Biochemical assays revealed that Memo is a copper-dependent redox enzyme that promoted a more oxidized intracellular milieu and stimulated the production of reactive oxygen species (ROS) in cellular structures involved in migration. Memo was also required for the sustained production of the ROS O2- by NADPH (reduced form of nicotinamide adenine dinucleotide phosphate) oxidase 1 (NOX1) in breast cancer cells. Memo abundance was increased in >40% of the primary breast tumors tested, was correlated with clinical parameters of aggressive disease, and was an independent prognostic factor of early distant metastasis.
Memo是一种进化上保守的蛋白质,在细胞运动中起关键作用。我们发现,Memo对于乳腺癌细胞在体外的迁移和侵袭以及体内乳腺癌细胞异种移植的自发性肺转移是必需的。生化分析表明,Memo是一种铜依赖性氧化还原酶,它促进细胞内环境更加氧化,并刺激参与迁移的细胞结构中活性氧(ROS)的产生。Memo也是乳腺癌细胞中烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶1(NOX1)持续产生活性氧O2-所必需的。在超过40%的测试原发性乳腺肿瘤中,Memo的丰度增加,与侵袭性疾病的临床参数相关,并且是早期远处转移的独立预后因素。