Bahrami Afsane, Amerizadeh Forouzan, Hassanian Seyed Mahdi, ShahidSales Soodabeh, Khazaei Majid, Maftouh Mina, Ghayour-Mobarhan Majid, Ferns Gordon A, Avan Amir
Department of Modern Sciences and Technologies, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Student Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
J Cell Physiol. 2018 Mar;233(3):2193-2201. doi: 10.1002/jcp.25966. Epub 2017 May 23.
Chemotherapy regimen containing oxaliplatin is often the first-line treatment for patient with advanced colorectal cancer. Oxaliplatin binds to DNA, leading to the formation of crosslinks and bulky adducts. Approximately 50% of patients with CRC benefit from treatment with oxaliplatin. It is possible that genetic variants in biological pathways involved in drug transportation, drug metabolism, DNA damage repair, and cell cycle modulation might affect the activity, or efficacy of oxaliplatin. Because oxaliplatin resistance may be related to these genetic variants and may therefore be an important reason for treatment failure, we have summarized the genetic variations that have been reported to be predictive markers of the response to oxaliplatin based therapy in patients with advanced CRC.
含奥沙利铂的化疗方案通常是晚期结直肠癌患者的一线治疗方案。奥沙利铂与DNA结合,导致交联和大分子加合物的形成。约50%的结直肠癌患者从奥沙利铂治疗中获益。参与药物转运、药物代谢、DNA损伤修复和细胞周期调节的生物学途径中的基因变异可能会影响奥沙利铂的活性或疗效。由于奥沙利铂耐药可能与这些基因变异有关,因此可能是治疗失败的一个重要原因,我们总结了据报道可作为晚期结直肠癌患者奥沙利铂治疗反应预测标志物的基因变异。