Tyrosine kinase inhibitors enhanced the efficacy of conventional chemotherapeutic agent in multidrug resistant cancer cells

被引:83
作者
Wu, Shaocong [1 ]
Fu, Liwu [1 ]
机构
[1] Sun Yat Sen Univ, Canc Ctr, State Key Lab Oncol South China, Guangdong Esophageal Canc Inst, Guangzhou 510060, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Tyrosine kinase inhibitor; ABC transporter; Multiple drug resistance; Chemotherapy; Chemosensitizer; BINDING CASSETTE TRANSPORTER; G MEMBER 2; LAPATINIB PLUS CAPECITABINE; ANTICANCER DRUG-SENSITIVITY; SELECTIVE FGFR INHIBITOR; SUBFAMILY-B MEMBER-1; STEM-LIKE CELLS; IN-VITRO; P-GLYCOPROTEIN; ABC TRANSPORTERS;
D O I
10.1186/s12943-018-0775-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multidrug resistance (MDR) triggered by ATP binding cassette (ABC) transporter such as ABCB1, ABCC1, ABCG2 limited successful cancer chemotherapy. Unfortunately, no commercial available MDR modulator approved by FDA was used in clinic. Tyrosine kinase inhibitors (TKIs) have been administrated to fight against cancer for decades. Almost TKI was used alone in clinic. However, drug combinations acting synergistically to kill cancer cells have become increasingly important in cancer chemotherapy as an approach for the recurrent resistant disease. Here, we summarize the effect of TKIs on enhancing the efficacy of conventional chemotherapeutic drug in ABC transporter-mediated MDR cancer cells, which encourage to further discuss and study in clinic.
引用
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页数:13
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