Humphreys Robin C, Halpern Wendy
Human Genome Sciences, Oncology Research Department, Rockville, MD 20850, USA.
Adv Exp Med Biol. 2008;615:127-58. doi: 10.1007/978-1-4020-6554-5_7.
A human tumor cell's ability to avoid the normal regulatory mechanisms of cell growth, division, and death are the hallmarks of transformation and cancer. Numerous novel therapeutic agents currently in preclinical or clinical evaluation aim to revive the normal regulation or evade these regulatory defects and induce growth arrest and cell death. One of the cell death pathways that has garnered significant interest, as a potential target for therapeutic intervention, is the programmed cell death pathway regulated by the tumor necrosis factor-related apoptosis-inducing ligand receptors (TRAIL-RS). Receptor agonist molecules including forms of the native ligand and monoclonal antibodies are being developed and tested as therapeutics in the treatment of human cancer.
人类肿瘤细胞规避细胞生长、分裂和死亡正常调控机制的能力是细胞转化和癌症的标志。目前许多处于临床前或临床评估阶段的新型治疗药物旨在恢复正常调控或规避这些调控缺陷,从而诱导生长停滞和细胞死亡。作为治疗干预的潜在靶点,一种引起广泛关注的细胞死亡途径是由肿瘤坏死因子相关凋亡诱导配体受体(TRAIL-RS)调控的程序性细胞死亡途径。包括天然配体形式和单克隆抗体在内的受体激动剂分子正在被开发并作为治疗人类癌症的药物进行测试。