Drug resistance, predictive markers and pharmacogenomics in colorectal cancer

被引:158
作者
Longley, Daniel B. [1 ]
Allen, Wendy L. [1 ]
Johnston, Patrick G. [1 ]
机构
[1] Queens Univ Belfast, Ctr Canc Res & Cell Biol, Drug Resistance Lab, Belfast BT12 6BJ, Antrim, North Ireland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2006年 / 1766卷 / 02期
关键词
drug resistance; colorectal cancer; pharmacogenomics; predictive marker;
D O I
10.1016/j.bbcan.2006.08.001
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
Resistance to chemotherapy limits the effectiveness of current cancer therapies, including those used to treat colorectal cancer, which is the second most common cause of cancer death in Europe and the United States. 5-Fluorouracil-based chemotherapy regimens are the standard treatment for colorectal cancer in both the adjuvant and advanced disease settings. Drug resistance is thought to cause treatment failure in over 90% of patients with metastatic cancer, while drug resistant micrometastic tumour cells may also reduce the impact of adjuvant chemotherapy treatment. The identification of panels of biomarkers that not only identify those patients most likely to benefit from chemotherapy treatment, but also which chemotherapies to use, would be a major advance. In this review, we describe molecular mechanisms of drug resistance that may be relevant to colorectal cancer. We also describe the results of predictive biomarker studies in this disease. Finally, we discuss how pharmacogenomics and other high through-put technologies may impact on the clinical management of colorectal cancer in the future. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:184 / 196
页数:13
相关论文
共 160 条
[1]   Immunoreactive dUMP and TTP pools as an index of thymidylate synthase inhibition; Effect of Tomudex (ZD1694) and a nonpolyglutamated quinazoline antifolate (CB30900) in L1210 mouse leukaemia cells [J].
Aherne, GW ;
Hardcastle, A ;
Raynaud, F ;
Jackman, AL .
BIOCHEMICAL PHARMACOLOGY, 1996, 51 (10) :1293-1301
[2]   Eniluracil treatment completely inactivates dihydropyrimidine dehydrogenase in colorectal tumors [J].
Ahmed, FY ;
Johnston, SJ ;
Cassidy, J ;
O'Kelly, T ;
Binnie, N ;
Murray, GI ;
van Gennip, AH ;
Abeling, NGGM ;
Knight, S ;
McLeod, HL .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (08) :2439-2445
[3]  
Ahnen DJ, 1998, CANCER RES, V58, P1149
[4]  
Allegra CJ, 2003, NEW ENGL J MED, V349, P1774
[5]   Biochemical, cellular, and pharmacological aspects of the multidrug transporter [J].
Ambudkar, SV ;
Dey, S ;
Hrycyna, CA ;
Ramachandra, M ;
Pastan, I ;
Gottesman, MM .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1999, 39 :361-398
[6]  
Ando Y, 2000, CANCER RES, V60, P6921
[7]   Molecular mechanisms of action and prediction of response to oxaliplatin in colorectal cancer cells [J].
Arango, D ;
Wilson, AJ ;
Shi, Q ;
Corner, GA ;
Arañes, MJ ;
Nicholas, C ;
Lesser, M ;
Mariadason, JM ;
Augenlicht, LH .
BRITISH JOURNAL OF CANCER, 2004, 91 (11) :1931-1946
[8]   Cellular determinants of oxaliplatin sensitivity in colon cancer cell lines [J].
Arnould, S ;
Hennebelle, I ;
Canal, P ;
Bugat, R ;
Guichard, S .
EUROPEAN JOURNAL OF CANCER, 2003, 39 (01) :112-119
[9]   Who will benefit from treatment against EGFR? [J].
Arribas, J ;
Baselga, J .
LANCET ONCOLOGY, 2005, 6 (05) :257-258
[10]   5-Fluorouracil induced Fas upregulation associated with apoptosis in liver metastases of colorectal cancer patients [J].
Backus, HHJ ;
Dukers, DF ;
van Groeningen, CJ ;
Vos, W ;
Bloemena, E ;
Wouters, D ;
van Riel, JMGH ;
Smid, K ;
Giaccone, G ;
Pinedo, HM ;
Peters, GJ .
ANNALS OF ONCOLOGY, 2001, 12 (02) :209-216