Gemcitabine: Metabolism and molecular mechanisms of action, sensitivity and chemoresistance in pancreatic cancer

被引:0
作者
Cavalcante, Lucas de Sousa [1 ]
Monteiro, Gisele [1 ]
机构
[1] Univ Sao Paulo, FCF, Dept Tecnol Bioquim Farmaceut, BR-05508000 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Chemoresistance; Pancreatic tumor; Gemcitabine resistance; Molecular targets; NF kappa B; CELL LUNG-CANCER; NF-KAPPA-B; ACTIVATED PROTEIN-KINASE; EQUILIBRATIVE NUCLEOSIDE TRANSPORTER-1; HEDGEHOG SIGNALING PATHWAY; SMALL INTERFERING RNA; REDUCTASE SUBUNIT M1; GROWTH IN-VIVO; DEOXYCYTIDINE KINASE; SONIC HEDGEHOG;
D O I
10.1010/j.ejphar.2014.07.041
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gemcitabine is the first-line treatment for pancreatic adenocarcinoma, but is increasingly used to treat breast, bladder, and non-small cell lung cancers. Despite such broad use, intrinsic and acquired chemoresistance is common. In general, the underlying mechanisms of chemoresistance are poorly understood. Here, current knowledge of gemcitabine metabolism, mechanisms of action, sensitivity and chemoresistance reported over the past two decades are reviewed; and we also offer new perspectives to improve gemcitabine efficacy with particular reference to the treatment of pancreatic cancer. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:8 / 16
页数:9
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