Laboratory of Biochemistry, Research Unit 02/UR/09-01, High Institute of Biotechnology, Institut Supérieur de Biotechnologie, BP 74, Avenue Tahar Haddad, Monastir 5000, Tunisia.
Med Oncol. 2010 Jun;27(2):185-98. doi: 10.1007/s12032-009-9190-3. Epub 2009 Mar 11.
Tumor necrosis factor (TNF)-alpha is implicated in the same time in apoptosis and in cell proliferation. TNF-alpha not only acts as pro-inflammatory cytokine conducing to wide spectrum of human diseases including inflammatory diseases, but can also induce tumor development. The molecular mechanisms of TNF-alpha functions have been intensively investigated. In this review we covered TNF-alpha, the molecule, its signaling pathway, and its therapeutic functions. We provide a particular insight in its paradoxical role in tumor promotion and in its use as anti-tumor agent. This review considers also the recent findings regarding TNF-alpha inhibitors, their pharmacokinetics, and their pharmacodynamics. Six TNF-alpha inhibitors have been considered here: Infliximab, Adalimumab, Golimumab, CDP870, CDP571, Etanercept, and Thalidomide. We discussed the clinical relevance of their functions in treatment of several diseases such as advanced inflammatory rheumatic and bowel disease, with a focus in cancer treatment. Targeting TNF-alpha by these drugs has many side effects like malignancies development, and the long-term sequels are not very well explored. Their efficacy and their safety were discussed, underscoring the necessity of close patients monitoring and of their caution use.
肿瘤坏死因子 (TNF)-α 同时参与细胞凋亡和增殖。TNF-α 不仅作为促炎细胞因子,导致包括炎症性疾病在内的广泛人类疾病,还可诱导肿瘤发展。TNF-α 功能的分子机制已得到深入研究。在本综述中,我们涵盖了 TNF-α 分子、其信号通路及其治疗功能。我们特别探讨了其在肿瘤促进中的矛盾作用及其作为抗肿瘤药物的用途。本综述还考虑了关于 TNF-α 抑制剂的最新发现,包括它们的药代动力学和药效动力学。这里考虑了六种 TNF-α 抑制剂:英夫利昔单抗、阿达木单抗、戈利木单抗、CDP870、CDP571、依那西普和沙利度胺。我们讨论了它们在治疗多种疾病(如晚期炎症性风湿性疾病和肠道疾病)中的临床相关性,重点关注癌症治疗。这些药物通过靶向 TNF-α 具有许多副作用,如恶性肿瘤的发展,其长期后果尚未得到很好的探索。我们讨论了它们的疗效和安全性,强调了密切监测患者和谨慎使用的必要性。