Puyo Stéphane, Montaudon Danièle, Pourquier Philippe
INSERM U916, Institut Bergonié, 229 cours de l'Argonne, 33076 Bordeaux cedex, France.
INSERM U916, Institut Bergonié, 229 cours de l'Argonne, 33076 Bordeaux cedex, France.
Crit Rev Oncol Hematol. 2014 Jan;89(1):43-61. doi: 10.1016/j.critrevonc.2013.07.006. Epub 2013 Aug 20.
Alkylating agents represent the oldest class of anticancer agents with the approval of mechloretamine by the FDA in 1949. Even though their clinical use is far beyond the use of new targeted therapies, they still occupy a major place in the treatment of specific malignancies, sometimes representing the unique option for the treatment of refractory tumors. Here, we are reviewing the major classes of alkylating agents, with a particular focus on the latest generations of compounds that specifically target the minor groove of the DNA. These naturally occurring derivatives have a unique mechanism of action that explains the recent regain of interest in developing new classes of alkylating agents that could be used in combination with other anticancer drugs to enhance tumor response in the clinic.
烷基化剂是最古老的一类抗癌药物,1949年美法仑获美国食品药品监督管理局(FDA)批准。尽管它们的临床应用远比新的靶向疗法广泛,但在特定恶性肿瘤的治疗中仍占据重要地位,有时是治疗难治性肿瘤的唯一选择。在此,我们综述烷基化剂的主要类别,特别关注最新一代特异性靶向DNA小沟的化合物。这些天然存在的衍生物具有独特的作用机制,这解释了近期人们为何重新对开发可与其他抗癌药物联合使用以增强临床肿瘤反应的新型烷基化剂产生兴趣。