Targeting the Fas/FasL signaling pathway in cancer therapy

被引:192
作者
Villa-Morales, Maria
Fernandez-Piqueras, Jose [1 ]
机构
[1] Univ Autonoma Madrid, Ctr Biol Mol Severo Ochoa CSIC UAM, CIBERER, ISCIII, Madrid, Spain
关键词
apoptosis; combined therapy; Fas/CD95; FasL/CD95L; resistance; sensitization; therapy; NF-KAPPA-B; FAS-MEDIATED APOPTOSIS; CELL-SURFACE ANTIGEN; DEATH RECEPTOR; UP-REGULATION; PROSTATE-CANCER; DOWN-REGULATION; TUMOR-CELLS; MOLECULAR-CLONING; INDUCE APOPTOSIS;
D O I
10.1517/14728222.2011.628937
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: The Fas/FasL system plays a significant role in tumorigenesis. Research has shown that its impairment in cancer cells may lead to apoptosis resistance and contribute to tumor progression. Thus, the development of effective therapies targeting the Fas/FasL system may play an important role in the fight against cancer. Areas covered: In this review the recent literature on targeting the Fas/FasL system for therapeutic exploitation at different levels is reviewed. Promising pre-clinical approaches and various exceptions are highlighted. The potential of combined therapies is also explored, whereby tumor sensitivity to Fas-mediated apoptosis is restored, before an effective targeted therapy is employed. Expert opinion: The success of the Fas/FasL system targeting for therapeutics will require a better understanding of the alterations conferring resistance, in order to use the most appropriate sensitizing chemotherapeutic or radio-therapeutic agents in combination with effective targeted therapies.
引用
收藏
页码:85 / 101
页数:17
相关论文
共 157 条
[1]
Molecular ordering of the initial signaling events of CD95 [J].
Algeciras-Schimnich, A ;
Shen, L ;
Barnhart, BC ;
Murmann, AE ;
Burkhardt, JK ;
Peter, ME .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (01) :207-220
[2]
The Role of MMP7 and Its Cross-Talk with the FAS/FASL System during the Acquisition of Chemoresistance to Oxaliplatin [J].
Almendro, Vanessa ;
Ametller, Elisabet ;
Garcia-Recio, Susana ;
Collazo, Olga ;
Casas, Ignasi ;
Auge, Josep M. ;
Maurel, Joan ;
Gascon, Pedro .
PLOS ONE, 2009, 4 (03)
[3]
Treatment of experimental glioma by administration of adenoviral vectors expressing Fas ligand [J].
Ambar, BB ;
Frei, K ;
Malipiero, U ;
Morelli, AE ;
Castro, MG ;
Lowenstein, PR ;
Fontana, A .
HUMAN GENE THERAPY, 1999, 10 (10) :1641-1648
[4]
Differential regulation of MMP7 in colon cancer cells resistant and sensitive to oxaliplatin-induced cell death [J].
Ametller, Elisabet ;
Garcia-Recio, Susana ;
Pastor-Arroyo, Eva-Maria ;
Callejo, Gerard ;
Carbo, Neus ;
Gascon, Pedro ;
Almendro, Vanessa .
CANCER BIOLOGY & THERAPY, 2011, 11 (01) :4-13
[5]
Understanding rituximab function and resistance: implications for tailored therapy [J].
Amoroso, Alfredo ;
Hafsi, Sameh ;
Militello, Loredana ;
Russo, Alessia E. ;
Soua, Zohra ;
Mazzarino, Maria C. ;
Stivala, Franca ;
Libra, Massimo .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2011, 16 :770-782
[6]
[Anonymous], FAS TNF RECEPTOR SUP
[7]
[Anonymous], FAS LIGAND TNF SUPER
[8]
Restricted expression of an adenoviral vector encoding Fas ligand (CD95L) enhances safety for cancer gene therapy [J].
Aoki, K ;
Akyürek, LM ;
San, H ;
Leung, K ;
Parmacek, MS ;
Nabel, EG ;
Nabel, GJ .
MOLECULAR THERAPY, 2000, 1 (06) :555-565
[9]
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
[10]
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