Edelman Martin J
University of Maryland Greenebaum Cancer Center, Baltimore, 21201, USA.
Clin Lung Cancer. 2005 Oct;7 Suppl 2:S64-6. doi: 10.3816/clc.2005.s.011.
The combination of chemotherapy and radiation has been validated for the treatment of locally advanced non-small-cell lung cancer (NSCLC). However, the results are still unsatisfactory, and there is a need to improve current treatment. One approach is to use new agents that have the potential to enhance the efficacy of chemotherapy, radiation therapy (RT), or both. One potential target is the ubiquitin-proteasome pathway. This pathway plays an essential role in the degradation of most short- and long-lived intracellular proteins in eukaryotic cells and therefore regulating the cell cycle, neoplastic growth, and metastasis. Bortezomib is a selective 26S proteasome inhibitor that has been approved for the treatment of multiple myeloma. Bortezomib has demonstrated in vitro chemotherapy- and RT-sensitizing properties as well as single-agent activity in lung cancer. This article will review the rationale for the use of bortezomib as part of the chemotherapy/RT strategy for the treatment of NSCLC.
化疗与放疗联合已被证实可用于治疗局部晚期非小细胞肺癌(NSCLC)。然而,结果仍不尽人意,因此有必要改进当前的治疗方法。一种方法是使用有可能提高化疗、放疗(RT)或两者疗效的新型药物。一个潜在靶点是泛素-蛋白酶体途径。该途径在真核细胞中大多数短寿命和长寿命细胞内蛋白质的降解中起关键作用,从而调节细胞周期、肿瘤生长和转移。硼替佐米是一种选择性26S蛋白酶体抑制剂,已被批准用于治疗多发性骨髓瘤。硼替佐米在体外已显示出化疗和放疗增敏特性以及在肺癌中的单药活性。本文将综述将硼替佐米用作NSCLC化疗/放疗策略一部分的理论依据。