University of Delaware, Newark, Delaware.
Nemours Center for Cancer and Blood Disorders, Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware.
Cancer Res. 2018 Jan 15;78(2):320-325. doi: 10.1158/0008-5472.CAN-17-2782. Epub 2018 Jan 8.
Preclinical and clinical development of agents that inhibit cell-cycle progression have brought an understanding of the feasibility of targeting various cell-cycle regulators in patients with cancer. Small molecule inhibitors targeting key proteins that participate in cell-cycle progression including the cyclin-dependent kinases and checkpoint kinases induce cell-cycle arrest and apoptosis in neoplastic cells. Early phase I studies demonstrate targeted inhibitors can be administered safely in adult and pediatric cancer patients, but these agents generally show limited clinical benefits as single agents. In this review, we discuss biological mechanisms that support dual combination strategies of cell-cycle inhibition with chemotherapeutic agents that are anticipated to achieve rationally targeted therapies for cancer patients. The rationale for evaluating these combination strategies is that DNA damage renders tumors highly responsive to irreversible cell-cycle arrest therapy. This approach is predicted to generate less intensive therapies and to maximize the efficacy of individual agents against solid tumors and hematologic malignancies. .
在抑制细胞周期进程的药物的临床前和临床开发中,人们已经了解到在癌症患者中靶向各种细胞周期调节剂的可行性。针对参与细胞周期进程的关键蛋白的小分子抑制剂,包括细胞周期蛋白依赖性激酶和检查点激酶,可诱导肿瘤细胞的细胞周期停滞和凋亡。早期的 I 期研究表明,靶向抑制剂可以安全地用于成人和儿科癌症患者,但这些药物作为单一药物通常显示出有限的临床获益。在这篇综述中,我们讨论了支持细胞周期抑制与化疗药物双重联合策略的生物学机制,预计这些策略将为癌症患者实现合理靶向治疗。评估这些联合策略的理由是,DNA 损伤使肿瘤对不可逆的细胞周期停滞治疗高度敏感。这种方法预计会产生更少的强化治疗,并最大限度地提高针对实体瘤和血液恶性肿瘤的单个药物的疗效。