Review of recent studies on resistance to cytotoxic deoxynucleoside analogues

被引:78
作者
Jordheim, Lars Petter
Dumontet, Charles
机构
[1] Int Agcy Res Canc, F-69372 Lyon 08, France
[2] Univ Lyon, F-69008 Lyon, France
[3] INSERM, U590, F-69008 Lyon, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2007年 / 1776卷 / 02期
关键词
deoxynucleoside analogues; cancer; resistance; polymorphism; pronucleotide; conjugate;
D O I
10.1016/j.bbcan.2007.07.004
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
Cytotoxic deoxynucleoside analogues are widely used in the treatment of haematological malignancies and solid tumours. Their metabolism and mechanisms of action are relatively well known, but with ongoing technological development, a continuous flow of scientific data is constantly adding new knowledge to this field. Thus, what was already a well-developed area some years ago has continued its expansion and become a better understood part of medical sciences. In order to keep abreast of the latest advances on cellular and clinical resistance to deoxynucleoside analogues, we have reviewed the recent literature and provide here an update on the subject. We have particularly focused on changes in gene products involved in the metabolic pathway of these drugs, such as membrane transporters, kinases, deaminases and 5'-nucleotidases. We also gave an overview on the chemical and biological development of modified deoxynucleoside analogues such as conjugates and pronucleotides. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 159
页数:22
相关论文
共 214 条
[41]  
DAMARAJU S, 2005, GENOMICS, V15, P173
[42]   Nucleoside anticancer drugs: the role of nucleoside transporters in resistance to cancer chemotherapy [J].
Damaraju, VL ;
Damaraju, S ;
Young, JD ;
Baldwin, SA ;
Mackey, J ;
Sawyer, MB ;
Cass, CE .
ONCOGENE, 2003, 22 (47) :7524-7536
[43]   An increase in the expression of ribonucleotide reductase large subunit 1 is associated with gemcitabine resistance in non-small cell lung cancer cell lines [J].
Davidson, JD ;
Ma, LD ;
Flagella, M ;
Geeganage, S ;
Gelbert, LM ;
Slapak, CA .
CANCER RESEARCH, 2004, 64 (11) :3761-3766
[44]  
DAVIDSON JD, 2002, P AM ASSOC CANC RES, V43, P3868
[45]   Enforced expression of the tumor suppressor p53 renders human leukemia cells (U937) more sensitive to 1-[β-D-arabinofuranosyl]cytosine (ara-C)-induced apoptosis [J].
Decker, RH ;
Levin, J ;
Kramer, LB ;
Dai, Y ;
Grant, S .
BIOCHEMICAL PHARMACOLOGY, 2003, 65 (12) :1997-2008
[46]   A phase I study of antisense oligonucleotide GTI-2040 given by continuous intravenous infusion in patients with advanced solid tumors [J].
Desai, AA ;
Schilsky, RL ;
Young, A ;
Janisch, L ;
Stadler, WM ;
Vogelzang, NJ ;
Cadden, S ;
Wright, JA ;
Ratain, MJ .
ANNALS OF ONCOLOGY, 2005, 16 (06) :958-965
[47]  
Duxbury M.S., 2004, SURGERY, V136, P261
[48]   RRM2 induces NF-κB-dependent MMP-9 activation and enhances cellular invasiveness [J].
Duxbury, Mark S. ;
Whang, Edward E. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 354 (01) :190-196
[49]   RETRACTED: RNA interference targeting the M2 subunit of ribonucleotide reductase enhances pancreatic adenocarcinoma chemosensitivity to gemcitabine (Retracted article. See FEB, 2023) [J].
Duxbury, MS ;
Ito, H ;
Zinner, MJ ;
Ashley, SW ;
Whang, EE .
ONCOGENE, 2004, 23 (08) :1539-1548
[50]   A novel role for carcinoembryonic antigen-related cell adhesion molecule 6 as a determinant of gemcitabine chemoresistance in pancreatic adenocarcinoma cells [J].
Duxbury, MS ;
Ito, H ;
Benoit, E ;
Waseem, T ;
Ashley, SW ;
Whang, EE .
CANCER RESEARCH, 2004, 64 (11) :3987-3993