Does CD95 have tumor promoting activities?

被引:84
作者
Peter, ME [1 ]
Legembre, P [1 ]
Barnhart, BC [1 ]
机构
[1] Univ Chicago, Ben May Inst Canc Res, Chicago, IL 60637 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2005年 / 1755卷 / 01期
关键词
D O I
10.1016/j.bbcan.2005.01.001
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
CD95 (APO-1/Fas) is an important inducer of the extrinsic apoptosis signaling pathway and therapy induced apoptosis of many tumor cells has been linked to the activity of CD95. Changes in the expression of CD95 and/or its ligand CD95L are frequently found in human cancer. The downregulation or mutation of CD95 has been proposed as a mechanism by which cancer cells avoid destruction by the immune system through reduced apoptosis sensitivity. CD95 has therefore been viewed as a tumor suppressor. Furthermore, increased CD95L concentration in tumor patients has been linked to tumor cells killing infiltrating lymphocytes in a process called "the tumor counter attack". Recent data have illuminated unknown activities of CD95 in tumor cells with downregulated or mutated CD95 in the presence of increased CD95L. Under these conditions the stimulation of CD95 signals nonapoptotic pathways, activating NF-kappa B and MAP kinases for example, which may result in the induction of tumorigenic or prosurvival genes. A new model of CD95 functions is proposed in which CD95 is converted from a tumor suppressor to a tumor promoter by a single point mutation in one of the CD95 alleles, a situation frequently found in advanced human cancer, resulting in apoptosis resistance and activation of tumorigenic pathways. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 36
页数:12
相关论文
共 151 条
[1]   Early activation of caspases during T lymphocyte stimulation results in selective substrate cleavage in nonapoptotic cells [J].
Alam, A ;
Cohen, LY ;
Aouad, S ;
Sékaly, RP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (12) :1879-1890
[2]   FAS TRANSDUCES ACTIVATION SIGNALS IN NORMAL HUMAN T-LYMPHOCYTES [J].
ALDERSON, MR ;
ARMITAGE, RJ ;
MARASKOVSKY, E ;
TOUGH, TW ;
ROUX, E ;
SCHOOLEY, K ;
RAMSDELL, F ;
LYNCH, DH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (06) :2231-2235
[3]   Two CD95 tumor classes with different sensitivities to antitumor drugs [J].
Algeciras-Schimnich, A ;
Pietras, EM ;
Barnhart, BC ;
Legembre, P ;
Vijayan, S ;
Holbeck, SL ;
Peter, ME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (20) :11445-11450
[4]   Extracellular matrix interacts with soluble CD95L: Retention and enhancement of cytotoxicity [J].
Aoki, K ;
Kurooka, M ;
Chen, JJ ;
Petryniak, J ;
Nabel, EG ;
Nabel, GJ .
NATURE IMMUNOLOGY, 2001, 2 (04) :333-337
[5]   Gene transfer of Fas ligand induces tumor regression in vivo [J].
Arai, H ;
Gordon, D ;
Nabel, EG ;
Nabel, GJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (25) :13862-13867
[6]   Activation and activities of the p53 tumour suppressor protein [J].
Bálint, É ;
Vousden, KH .
BRITISH JOURNAL OF CANCER, 2001, 85 (12) :1813-1823
[7]   CD95 apoptosis resistance in certain cells can be overcome by noncanonical activation of caspase-8 [J].
Barnhart, BC ;
Pietras, EM ;
Algeciras-Schimnich, A ;
Salmena, L ;
Sayama, K ;
Hakem, R ;
Peter, ME .
CELL DEATH AND DIFFERENTIATION, 2005, 12 (01) :25-37
[8]   CD95 ligand induces motility and invasiveness of apoptosis-resistant tumor cells [J].
Barnhart, BC ;
Legembre, P ;
Pietras, E ;
Bubici, C ;
Franzoso, G ;
Peter, ME .
EMBO JOURNAL, 2004, 23 (15) :3175-3185
[9]   The CD95 type I/type II model [J].
Barnhart, BC ;
Alappat, EC ;
Peter, ME .
SEMINARS IN IMMUNOLOGY, 2003, 15 (03) :185-193
[10]  
Bellone G, 2000, CLIN CANCER RES, V6, P2448