Defective core-apoptosis signalling in diffuse malignant pleural mesothelioma: opportunities for effective drug development

被引:70
作者
Fennell, DA
Rudd, RM
机构
[1] Univ London St Bartholomews Hosp Med Coll, Dept Med Oncol, London EC1A 7BE, England
[2] Univ London St Bartholomews Hosp Med Coll, Lung Canc & Mesothelioma Res Grp, London EC1A 7BE, England
关键词
D O I
10.1016/S1470-2045(04)01492-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Because of a lack of effective treatments, survival from diffuse pleural mesothelioma remains poor. Many people do not think that treatments for this disease are effective. The understanding of the biology of mesothelioma relevant to the apoptosis-resistant phenotype has been slow to advance. However, this is now changing, and strategies for rational therapeutic drug development are emerging that have the potential to change the natural history and improve survival in the increasing number of patients that will be diagnosed in the next two decades. This review discusses recent developments in apoptosis biology that are specific to mesothelioma and the therapeutic implications for this aggressive cancer.
引用
收藏
页码:354 / 362
页数:9
相关论文
共 60 条
[1]  
Bénard F, 1999, J NUCL MED, V40, P1241
[2]   EXPRESSION OF GROWTH-FACTOR AND GROWTH-FACTOR RECEPTOR RNA IN RAT PLEURAL MESOTHELIAL CELLS IN CULTURE [J].
BERMUDEZ, E ;
EVERITT, J ;
WALKER, C .
EXPERIMENTAL CELL RESEARCH, 1990, 190 (01) :91-98
[3]   Histone deacetylase inhibitor downregulation of bcl-xl gene expression leads to apoptotic cell death in mesothelioma [J].
Cao, XBX ;
Mohuiddin, I ;
Ece, F ;
McConkey, DJ ;
Smythe, WR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2001, 25 (05) :562-568
[4]   Simian virus-40 large-T antigen binds p53 in human mesotheliomas [J].
Carbone, M ;
Rizzo, P ;
Grimley, PM ;
Procopio, A ;
Mew, DJY ;
Shridhar, V ;
DeBartolomeis, A ;
Esposito, V ;
Giuliano, MT ;
Steinberg, SM ;
Levine, AS ;
Giordano, A ;
Pass, HI .
NATURE MEDICINE, 1997, 3 (08) :908-912
[5]  
Chresta CM, 1996, CANCER RES, V56, P1834
[6]   Oxidation of a critical thiol residue of the adenine nucleotide translocator enforces Bcl-2-independent permeability transition pore opening and apoptosis [J].
Costantini, P ;
Belzacq, AS ;
La Vieira, H ;
Larochette, N ;
de Pablo, MA ;
Zamzami, N ;
Susin, SA ;
Brenner, C ;
Kroemer, G .
ONCOGENE, 2000, 19 (02) :307-314
[7]   AKT and the phosphatidylinositol 3-kinase/AKT pathway: Important molecular targets for lung cancer prevention and treatment [J].
Crowell, JA ;
Steele, VE .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (04) :252-253
[8]   Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery [J].
Datta, SR ;
Dudek, H ;
Tao, X ;
Masters, S ;
Fu, HA ;
Gotoh, Y ;
Greenberg, ME .
CELL, 1997, 91 (02) :231-241
[9]   MALIGNANT PLEURAL MESOTHELIOMA AND EPIDERMAL GROWTH-FACTOR RECEPTOR (EGF-R) - RELATIONSHIP OF EGF-R WITH HISTOLOGY AND SURVIVAL USING FIXED PARAFFIN EMBEDDED TISSUE AND THE F4, MONOCLONAL-ANTIBODY [J].
DAZZI, H ;
HASLETON, PS ;
THATCHER, N ;
WILKES, S ;
SWINDELL, R ;
CHATTERJEE, AK .
BRITISH JOURNAL OF CANCER, 1990, 61 (06) :924-926
[10]   The permeability transition pore signals apoptosis by directing Bax translocation and multimerization [J].
De Giorgi, F ;
Lartigue, L ;
Bauer, MKA ;
Schubert, A ;
Grimm, S ;
Hanson, GT ;
Remington, SJ ;
Youle, RJ ;
Ichas, F .
FASEB JOURNAL, 2002, 16 (02) :607-+