Tumor-Related Molecular Mechanisms of Oxaliplatin Resistance

被引:285
作者
Martinez-Balibrea, Eva [1 ,2 ]
Martinez-Cardus, Anna [3 ]
Gines, Alba [2 ]
Ruiz de Porras, Vicenc [2 ]
Moutinho, Catia [3 ]
Layos, Laura [1 ]
Luis Manzano, Jose [1 ]
Buges, Cristina
Bystrup, Sara [2 ]
Esteller, Manel [3 ,4 ,5 ]
Abad, Albert [1 ,2 ,6 ]
机构
[1] Hosp Badalona Germans Trias & Pujol, Med Oncol Serv, ICO, Barcelona 08916, Spain
[2] Inst Germans Trias & Pujol Fdn IGTP, Hlth Sci Res Inst, Badalona, Catalonia, Spain
[3] Bellvitge Biomed Res Inst IDIBELL, PEBC, Barcelona, Catalonia, Spain
[4] Univ Barcelona, Sch Med, Dept Physiol Sci 2, Barcelona, Catalonia, Spain
[5] ICREA, Barcelona, Catalonia, Spain
[6] Hosp CIMA Sanitas, Oncol Unit, Barcelona, Catalonia, Spain
关键词
COLORECTAL-CANCER PATIENTS; PLATINUM-BASED CHEMOTHERAPY; COMPLEMENTATION GROUP 1; BASE EXCISION-REPAIR; FACTOR-KAPPA-B; CELL-LINE; GENETIC POLYMORPHISMS; THYMIDYLATE SYNTHASE; ACQUIRED-RESISTANCE; FOLFOX-4; TREATMENT;
D O I
10.1158/1535-7163.MCT-14-0636
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oxaliplatin was the first platinum drug with proven activity against colorectal tumors, becoming a standard in the management of this malignancy. It is also considered for the treatment of pancreatic and gastric cancers. However, a major reason for treatment failure still is the existence of tumor intrinsic or acquired resistance. Consequently, it is important to understand the molecular mechanisms underlying the appearance of this phenomenon to find ways of circumventing it and to improve and optimize treatments. This review will be focused on recent discoveries about oxaliplatin tumor-related resistance mechanisms, including alterations in transport, detoxification, DNA damage response and repair, cell death (apoptotic and nonapoptotic), and epigenetic mechanisms.
引用
收藏
页码:1767 / 1776
页数:10
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