Isogawa Masato, Higuchi Masaya, Takahashi Masahiko, Oie Masayasu, Mori Naoki, Tanaka Yuetsu, Aoyagi Yutaka, Fujii Masahiro
Division of Virology, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-Dori, Niigata 951-8510, Japan.
Cancer Sci. 2008 Apr;99(4):792-8. doi: 10.1111/j.1349-7006.2008.00750.x.
Adult T-cell leukemia (ATL) is an aggressive type of leukemia, originating from T-cells infected with human T-cell leukemia virus type 1. Accumulating evidence suggests the aberrant activation of NF-kappaB to be a causative factor mediating the abnormal proliferation of leukemic cells, thus resulting in the development of ATL. A rearranged NF-kappa B2/p100 gene was isolated from an ATL-derived cell line, which was generated by a chromosomal translocation. The isolated NF-kappa B2 mutant is fused with the with no (lysine) deficient protein kinase 1 gene, coding for a 58 kDa protein that retains the DNA binding Rel homology domain, but it lacks the entire ankyrin repeat inhibitory domain, thus suggesting its constitutive activation. This rearranged NF-kappa B2 gene product (p58) was localized in the nucleus, and formed a complex with NF-kappaB p65 or RelB. Moreover, a T-cell line expressing p58 increased the amount of an NF-kappa B2-inducible gene, NF-kappa B2/p100 by itself. These results suggest that such NF-kappa B2 gene rearrangement may therefore be a factor in the constitutive activation of NF-kappaB in ATL, and thereby playing a role in the ATL pathogenesis.
成人T细胞白血病(ATL)是一种侵袭性白血病,起源于感染了1型人类T细胞白血病病毒的T细胞。越来越多的证据表明,核因子κB(NF-κB)的异常激活是介导白血病细胞异常增殖的致病因素,从而导致ATL的发生。从一株由染色体易位产生的ATL来源的细胞系中分离出一个重排的NF-κB2/p100基因。分离出的NF-κB2突变体与无(赖氨酸)缺陷蛋白激酶1基因融合,编码一种58 kDa的蛋白质,该蛋白质保留了DNA结合Rel同源结构域,但缺少整个锚蛋白重复抑制结构域,因此提示其组成性激活。这种重排的NF-κB2基因产物(p58)定位于细胞核,并与NF-κB p65或RelB形成复合物。此外,表达p58的T细胞系自身增加了NF-κB2诱导基因NF-κB2/p100的量。这些结果表明,这种NF-κB2基因重排可能是ATL中NF-κB组成性激活的一个因素,从而在ATL发病机制中发挥作用。