Chemoprevention of pancreatic cancer: A review of the molecular pathways involved, and evidence for the potential for chemoprevention

被引:22
作者
Doucas, H.
Garcea, G.
Neal, C. P.
Manson, M. M.
Berry, D. P.
机构
[1] Leicester Gen Hosp, Bioctr, Dept Canc Studies & Mol Med, Leicester LE5 4PW, Leics, England
[2] Leicester Gen Hosp, Dept Hepatobiliary Surg, Leicester LE5 4PW, Leics, England
基金
英国医学研究理事会;
关键词
pancreatic cancer; chemoprevention; NSAIDS; COX-2; polyphenols;
D O I
10.1159/000094560
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Pancreatic cancer has a poor prognosis. The use of drugs or natural agents which inhibit or slow down tumour growth therefore has important potential in the development of future therapies. Methods: A literature search of the PubMed and ISI Web of Science databases was undertaken to review the current data available on the alterations in signalling pathways found in pancreatic carcinogenesis, in order to identify sites that could be targeted by chemopreventive agents. Several agents of particular relevance to pancreatic cancer were identified, and their possible mechanisms of action reviewed. Results: Chemopreventive agents such as non-steroidal anti-inflammatory drugs, green tea constituents, and antioxidants have been shown to target various steps in intracellular signalling pathways, particularly those controlling cell proliferation and survival. Work on cell lines and animal models has shown that some of these agents may be able to modulate the growth of pancreatic tumours. Initial clinical trials of some chemopreventives in pancreatic cancer have been undertaken, and have yielded mixed results, prompting the need for further studies. Conclusion: As the molecular pathology of pancreatic cancer becomes better understood, sites of action of chemopreventive substances have been uncovered. Several agents have shown promising results by their ability to inhibit pancreatic carcinogenesis in laboratory studies. If these effects can be successfully translated into human studies then these agents may prove to be valuable adjuvant therapies in the future. Copyright (C) 2006 S. Karger AG, Basel and IAP.
引用
收藏
页码:429 / 439
页数:11
相关论文
共 91 条
[1]
Cell cycle dysregulation by green tea polyphenol epigallocatechin-3-gallate [J].
Ahmad, N ;
Cheng, PY ;
Mukhtar, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 275 (02) :328-334
[2]
MOST HUMAN CARCINOMAS OF THE EXOCRINE PANCREAS CONTAIN MUTANT C-K-RAS GENES [J].
ALMOGUERA, C ;
SHIBATA, D ;
FORRESTER, K ;
MARTIN, J ;
ARNHEIM, N ;
PERUCHO, M .
CELL, 1988, 53 (04) :549-554
[3]
Anderson KE, 2002, J NATL CANCER I, V94, P1168, DOI 10.1093/jnci/94.15.1168
[4]
Aoki T, 2002, ONCOL REP, V9, P761
[5]
Effects of dietary beta-carotene and selenium on initiation and promotion of pancreatic carcinogenesis in azaserine-treated rats [J].
Appel, MJ ;
Woutersen, RA .
CARCINOGENESIS, 1996, 17 (07) :1411-1416
[6]
INHIBITORY EFFECTS OF MICRONUTRIENTS ON PANCREATIC CARCINOGENESIS IN AZASERINE-TREATED RATS [J].
APPEL, MJ ;
ROVERTS, G ;
WOUTERSEN, RA .
CARCINOGENESIS, 1991, 12 (11) :2157-2161
[7]
Araki Y, 2003, CANCER RES, V63, P728
[8]
Role of NF-κB and Akt/PI3K in the resistance of pancreatic carcinoma cell lines against gemcitabine-induced cell death [J].
Arlt, A ;
Gehrz, A ;
Müerköster, S ;
Vorndamm, J ;
Kruse, ML ;
Fölsch, UR ;
Schäfer, H .
ONCOGENE, 2003, 22 (21) :3243-3251
[9]
The PI 3-kinase/Akt signaling pathway is activated due to aberrant Pten expression and targets transcription factors NF-κB and c-Myc in pancreatic cancer cells [J].
Asano, T ;
Yao, YX ;
Zhu, JJ ;
Li, DH ;
Abbruzzese, JL ;
Reddy, SAG .
ONCOGENE, 2004, 23 (53) :8571-8580
[10]
A phase I trial of perillyl alcohol in patients with advanced solid tumors [J].
Azzoli, CG ;
Miller, VA ;
Ng, KK ;
Krug, LM ;
Spriggs, DR ;
Tong, WP ;
Riedel, ER ;
Kris, MG .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2003, 51 (06) :493-498