Ichikawa K, Liu W, Zhao L, Wang Z, Liu D, Ohtsuka T, Zhang H, Mountz J D, Koopman W J, Kimberly R P, Zhou T
Biomedical Research Laboratories, Sankyo Co., Tokyo, Japan.
Nat Med. 2001 Aug;7(8):954-60. doi: 10.1038/91000.
A novel anti-human DR5 monoclonal antibody, TRA-8, induces apoptosis of most tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-sensitive tumor cells both in vitro and in vivo. In contrast to both the membrane-bound form of human TRAIL, which induced severe hepatitis in mice, and the soluble form of human TRAIL, which induced apoptosis of normal human hepatocytes in vitro, TRA-8 did not induce significant cell death of normal human hepatocytes. However, both primary hepatocellular carcinoma cells and an established liver cancer cell line were highly susceptible to the killing mediated by TRA-8. We show here that elevated levels of cell-surface expression of DR5 and increased susceptibility to DR5-mediated apoptosis are characteristics of malignant tumor cells. In contrast, DR5 alone is not sufficient to trigger apoptosis of normal hepatocytes. Therefore, selective, specific targeting of DR5 with an agonistic antibody might be a safe and effective strategy for cancer therapy.
一种新型抗人DR5单克隆抗体TRA-8,在体外和体内均可诱导大多数对肿瘤坏死因子相关凋亡诱导配体(TRAIL)敏感的肿瘤细胞凋亡。与可诱导小鼠严重肝炎的人TRAIL膜结合形式以及可在体外诱导正常人肝细胞凋亡的人TRAIL可溶性形式不同,TRA-8不会诱导正常人肝细胞发生明显的细胞死亡。然而,原发性肝癌细胞和一种已建立的肝癌细胞系对TRA-8介导的杀伤高度敏感。我们在此表明,DR5细胞表面表达水平升高以及对DR5介导的凋亡敏感性增加是恶性肿瘤细胞的特征。相比之下,单独的DR5不足以触发正常肝细胞的凋亡。因此,用激动性抗体选择性、特异性地靶向DR5可能是一种安全有效的癌症治疗策略。