Wu Fangting, Chiocca Susanna, Beck William T, Mo Yin-Yuan
Department of Medical Microbiology, Southern Illinois University School of Medicine, Springfield, IL 62794, USA.
Mol Cancer Ther. 2007 Jun;6(6):1823-30. doi: 10.1158/1535-7163.MCT-06-0771.
An early gene product, Gam1, encoded by the avian adenovirus CELO, is an inhibitory protein for the sumoylation machinery, which has been implicated in regulating a variety of cellular pathways. In this study, we found that Gam1 effectively suppressed both constitutive and inducible sumoylation and caused significant cell growth inhibition. This Gam1-mediated cell growth inhibition was associated with induction of apoptosis. In particular, Gam1 induced caspase-3 activity as detected by immunostaining and Western blot. Of interest, like the Ubc9 dominant-negative mutant, Gam1 also sensitized cells to DNA-damaging agents such as topotecan and doxorubicin and non-DNA-damaging agents such as paclitaxel and vincristine. Taken together, our findings suggest that activation of the caspase pathways is at least in part responsible for the increased apoptosis in Gam1-expressing cells and, thus, contributes to the growth inhibition and enhanced chemosensitivity.
禽腺病毒CELO编码的一种早期基因产物Gam1是一种针对类泛素化修饰机制的抑制性蛋白,该机制与多种细胞信号通路的调控有关。在本研究中,我们发现Gam1能有效抑制组成型和诱导型类泛素化修饰,并导致显著的细胞生长抑制。这种由Gam1介导的细胞生长抑制与细胞凋亡的诱导有关。具体而言,通过免疫染色和蛋白质印迹检测发现Gam1可诱导caspase-3活性。有趣的是,与Ubc9显性负性突变体类似,Gam1还使细胞对拓扑替康和阿霉素等DNA损伤剂以及紫杉醇和长春新碱等非DNA损伤剂敏感。综上所述,我们的研究结果表明,caspase信号通路的激活至少部分导致了表达Gam1的细胞中凋亡增加,进而导致生长抑制和化疗敏感性增强。