Cyclooxygenase-2 (COX-2) - A therapeutic target in liver cancer?

被引:55
作者
Breinig, Marco [1 ]
Schirmacher, Peter [1 ]
Kern, Michael Andre [1 ]
机构
[1] Univ Hosp, Dept Gen Pathol, D-69120 Heidelberg, Germany
关键词
D O I
10.2174/138161207782360627
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Targeting COX-2, a key-enzyme of the prostaglandin metabolism, for the treatment of cancer has been in the focus of researchers for about a decade. However, only recently has this topic been related to hepatocellular carcinoma (HCC). HCC is one of the most common cancers and a growing health problem worldwide. At present, only few promising treatment options are available, accentuating the urgent need for novel therapeutic approaches. Since the first report of COX-2 overexpression in HCC, several findings support the notion that selective COX-2 inhibition proves to be beneficial in this malignancy. This review focuses on recent discoveries regarding the pro-tumorigenic potential of COX-2 in HCC and the functional effects of COX-2 inhibition on molecular mechanisms of this malignancy. Of clinical interest, promising data from in vivo experiments and case studies suggest a beneficial effect of COX-2 inhibitors for HCC-therapy. Detailed analysis of COX-2- activated pathways and related mechanisms may enable the evaluation and design of even more specific and combinatorial treatment approaches in the future.
引用
收藏
页码:3305 / 3315
页数:11
相关论文
共 166 条
[1]
Aspirin and NS-398 inhibit hepatocyte growth factor-induced invasiveness of human hepatoma cells [J].
Abiru, S ;
Nakao, K ;
Ichikawa, T ;
Migita, K ;
Shigeno, M ;
Sakamoto, M ;
Ishikawa, H ;
Hamasaki, K ;
Nakata, K ;
Eguchi, K .
HEPATOLOGY, 2002, 35 (05) :1117-1124
[2]
Abou-Shady M, 1999, Swiss Surg, V5, P102, DOI 10.1024/1023-9332.5.3.102
[3]
Host prostaglandin E2-EP3 signaling regulates tumor-associated angiogenesis and tumor growth [J].
Amano, H ;
Hayashi, J ;
Endo, H ;
Kitasato, H ;
Yamashina, S ;
Maruyama, T ;
Kobayashi, M ;
Satoh, K ;
Narita, M ;
Sugimoto, Y ;
Murata, T ;
Yoshimura, H ;
Narumiya, S ;
Majima, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (02) :221-232
[4]
Araki Y, 2003, CANCER RES, V63, P728
[5]
Bae SH, 2001, CLIN CANCER RES, V7, P1410
[6]
Gene expression of ABC proteins in hepatocellular carcinoma, perineoplastic tissue, and liver diseases [J].
Bonin, S ;
Pascolo, L ;
Crocé, LS ;
Stanta, G ;
Tiribelli, C .
MOLECULAR MEDICINE, 2002, 8 (06) :316-323
[7]
Dysregulation of growth factor signaling in human hepatocellular carcinoma [J].
Breuhahn, K. ;
Longerich, T. ;
Schirmacher, P. .
ONCOGENE, 2006, 25 (27) :3787-3800
[8]
Prostanoid receptors: Subtypes and signaling [J].
Breyer, RM ;
Bagdassarian, CK ;
Myers, SA ;
Breyer, MD .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2001, 41 :661-690
[9]
Clinical management of hepatocellular carcinoma.: Conclusions of the Barcelona-2000 EASL Conference [J].
Bruix, J ;
Sherman, M ;
Llovet, JM ;
Beaugrand, M ;
Lencioni, R ;
Burroughs, AK ;
Christensen, E ;
Pagliaro, L ;
Colombo, M ;
Rodés, J .
JOURNAL OF HEPATOLOGY, 2001, 35 (03) :421-430
[10]
Regulation of cyclooxygenase 2 expression in hepatocytes by CCAAT/enhancer-binding proteins [J].
Callejas, NA ;
Boscá, L ;
Williams, CS ;
DuBois, RN ;
Martín-Sanz, P .
GASTROENTEROLOGY, 2000, 119 (02) :493-501