Shair Kathy H Y, Bendt Katherine M, Edwards Rachel H, Bedford Elisabeth C, Nielsen Judith N, Raab-Traub Nancy
Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
PLoS Pathog. 2007 Nov;3(11):e166. doi: 10.1371/journal.ppat.0030166.
Latent membrane protein 1 (LMP1) is the major oncoprotein of Epstein-Barr virus (EBV). In transgenic mice, LMP1 promotes increased lymphoma development by 12 mo of age. This study reveals that lymphoma develops in B-1a lymphocytes, a population that is associated with transformation in older mice. The lymphoma cells have deregulated cell cycle markers, and inhibitors of Akt, NFkappaB, and Stat3 block the enhanced viability of LMP1 transgenic lymphocytes and lymphoma cells in vitro. Lymphoma cells are independent of IL4/Stat6 signaling for survival and proliferation, but have constitutively activated Stat3 signaling. These same targets are also deregulated in wild-type B-1a lymphomas that arise spontaneously through age predisposition. These results suggest that Akt, NFkappaB, and Stat3 pathways may serve as effective targets in the treatment of EBV-associated B cell lymphomas.
潜伏膜蛋白1(LMP1)是 Epstein-Barr 病毒(EBV)的主要癌蛋白。在转基因小鼠中,LMP1促进12月龄时淋巴瘤发展增加。本研究揭示淋巴瘤在B-1a淋巴细胞中发生,该细胞群体与老年小鼠的转化相关。淋巴瘤细胞具有失调的细胞周期标志物,并且Akt、NFκB和Stat3的抑制剂在体外阻断LMP1转基因淋巴细胞和淋巴瘤细胞的增强活力。淋巴瘤细胞在存活和增殖方面不依赖IL4/Stat6信号传导,但具有组成性激活的Stat3信号传导。这些相同的靶点在通过年龄易感性自发产生的野生型B-1a淋巴瘤中也失调。这些结果表明,Akt、NFκB和Stat3途径可能是治疗EBV相关B细胞淋巴瘤的有效靶点。