The development of targeted therapies for hepatocellular cancer

被引:7
作者
Chattopadhyay, D. [1 ]
Manas, D. M. [1 ]
Reeves, H. L. [1 ]
机构
[1] Newcastle Univ, No Inst Canc Res, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
关键词
hepatocellular cancer; new therapies; molecular targets; small molecule inhibitors; receptor tyrosine kinase;
D O I
10.2174/138161207782360717
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Present treatment options for hepatocellular cancer (HCC) are limited to those individuals with good liver function and early stage disease. Unfortunately this includes only a minority of patients, few of which are actually cured of their cancer. Over the last 15-20 years biotechnology has made a very significant impact on medical research, to the extent that we know very much more about the regulation of normal cell growth and death, as well as the mechanisms underlying its disruption in disease processes. This knowledge has and is being rapidly exploited by academic and pharmaceutical organisations, often in collaboration. The result is the development, testing and steady introduction of therapies that target specific abnormalities in cancer cells. Although the safety and effectiveness of the majority of these agents has yet to be established in cirrhotic patients with HCC, we are hopeful that we will shortly see an increase in effective treatment options available for clinical use this disease. This review focuses on aberrant cancer proteins and pathways relevant to HCC, as well as the novel therapies or strategies targeting them, that are currently in the development or testing stages.
引用
收藏
页码:3292 / 3300
页数:9
相关论文
共 94 条
[1]   Disruption of the p16/cyclin D1/retinoblastoma protein pathway in the majority of human hepatocellular carcinomas [J].
Azechi, H ;
Nishida, N ;
Fukuda, Y ;
Nishimura, T ;
Minata, M ;
Katsuma, H ;
Kuno, M ;
Ito, T ;
Komeda, T ;
Kita, R ;
Takahashi, R ;
Nakao, K .
ONCOLOGY, 2001, 60 (04) :346-354
[2]   Targeted therapy in advanced non-small cell lung cancer (NSCLC): Where do we stand? [J].
Azim, Hatem A., Jr. ;
Ganti, Apar Kishor .
CANCER TREATMENT REVIEWS, 2006, 32 (08) :630-636
[3]  
Bae SH, 2001, CLIN CANCER RES, V7, P1410
[4]   EVIDENCE THAT INDOMETHACIN REVERSIBLY INHIBITS CELL-GROWTH IN THE G1 PHASE OF THE CELL-CYCLE [J].
BAYER, BM ;
BEAVEN, MA .
BIOCHEMICAL PHARMACOLOGY, 1979, 28 (03) :441-443
[5]   EFFECT OF DIETARY RETINYL PALMITATE ON THE PROMOTION OF ALTERED HEPATIC FOCI BY 3,3',4,4'-TETRACHLOROBIPHENYL AND 2,2',4,4',5,5'-HEXACHLOROBIPHENYL IN RATS INITIATED WITH DIETHYLNITROSAMINE [J].
BERBERIAN, I ;
CHEN, LC ;
ROBINSON, FR ;
GLAUERT, HP ;
CHOW, CK ;
ROBERTSON, LW .
CARCINOGENESIS, 1995, 16 (02) :393-398
[6]   Management of hepatoceullular carcinoma [J].
Bruix, J ;
Sherman, M .
HEPATOLOGY, 2005, 42 (05) :1208-1236
[7]   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
[8]   Prognostic prediction and treatment strategy in hepatocellular carcinoma [J].
Bruix, J ;
Llovet, JM .
HEPATOLOGY, 2002, 35 (03) :519-524
[9]   A pilot phase II trial of valspodar modulation of multidrug resistance to paclitaxel in the treatment of metastatic carcinoma of the breast (E1195): A trial of the eastern cooperative oncology group [J].
Carlson, Robert W. ;
O'Neill, Anne M. ;
Goldstein, Lori J. ;
Sikic, Branimir I. ;
Abramson, Neil ;
Stewart, James A. ;
Davidson, Nancy E. ;
Wood, William C. .
CANCER INVESTIGATION, 2006, 24 (07) :677-681
[10]  
Chen XB, 2003, SPECTROSC SPECT ANAL, V23, P1