Autophagy signaling in cancer and its potential as novel target to improve anticancer therapy

被引:117
作者
Moretti, Luigi [1 ]
Yang, Eddy S. [1 ]
Kim, Kwang W. [1 ]
Lu, Bo [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Vanderbilt Ingram Canc Ctr, Dept Radiat Oncol,Vanderbilt Clin B902, Nashville, TN 37232 USA
关键词
autophagy; apoptosis; cancer; cell death; ER stress; mTOR; PERK; radiation; ENDOPLASMIC-RETICULUM STRESS; FATTY-ACID SYNTHASE; MALIGNANT GLIOMA-CELLS; ACUTE PROMYELOCYTIC LEUKEMIA; TUMOR-SUPPRESSOR GENE; PAN-CASPASE INHIBITOR; ARSENIC TRIOXIDE; PROSTATE-CANCER; BREAST-CANCER; DAP-KINASE;
D O I
10.1016/j.drup.2007.05.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Non-apoptotic forms of programmed cell death are targets for novel approaches in anticancer therapy. Indeed, cancer cells often present with mutations in the apoptotic machinery that result in resistance to most anticancer therapies and contribute to a relatively low response rate to therapies based on the use of pro-apoptotic strategies. (Macro-)autophagy can be a highly efficient mode of cell death induction by excessive self-digestion as demonstrated by our experiments that studied the effect of radiation to induce autophagy cell death in apoptosis-deficient cells. Despite current controversies on the possible role of autophagy in the process of carcinogenesis and cancer progression by promoting cell survival, autophagy can be seen as a backup cell death mechanism, when other cell death mechanisms fail. This review will focus oil the pathways linking autophagy and cancer that are relevant for target identification and on pharmaceuticals that can be utilized to improve cancer therapy by targeting the autophagic pathway. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:135 / 143
页数:9
相关论文
共 91 条
[1]   Arsenic trioxide induces apoptosis in neuroblastoma cell lines through the activation of caspase 3 in vitro [J].
Akao, Y ;
Nakagawa, Y ;
Akiyama, K .
FEBS LETTERS, 1999, 455 (1-2) :59-62
[2]   Targeting the Akt/mammalian target of rapamycin pathway for radiosensitization of breast cancer [J].
Albert, Jeffrey M. ;
Kim, Kwang Woon ;
Cao, Carolyn ;
Lu, Bo .
MOLECULAR CANCER THERAPEUTICS, 2006, 5 (05) :1183-1189
[3]   Zinc inhibits p75NTR-mediated apoptosis in chick neural retina [J].
Allington, C ;
Shamovsky, IL ;
Ross, GM ;
Riopelle, RJ .
CELL DEATH AND DIFFERENTIATION, 2001, 8 (05) :451-456
[4]   A role of the kinase mTOR in cellular transformation induced by the oncoproteins P3k and Akt [J].
Aoki, M ;
Blazek, E ;
Vogt, PK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (01) :136-141
[5]   The tumor suppressor PTEN positively regulates macroautophagy by inhibiting the phosphatidylinositol 3-kinase/protein kinase B pathway [J].
Arico, S ;
Petiot, A ;
Bauvy, C ;
Dubbelhuis, PF ;
Meijer, AJ ;
Codogno, P ;
Ogier-Denis, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (38) :35243-35246
[6]   How death shapes life during development [J].
Baehrecke, EH .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (10) :779-787
[7]   FAS expression inversely correlates with PTEN level in prostate cancer and a PI 3-kinase inhibitor synergizes with FAS siRNA to induce apoptosis [J].
Bandyopadhyay, S ;
Pai, SK ;
Watabe, M ;
Gross, SC ;
Hirota, S ;
Hosobe, S ;
Tsukada, T ;
Miura, K ;
Saito, K ;
Markwell, SJ ;
Wang, Y ;
Huggenvik, J ;
Pauza, ME ;
Iiizumi, M ;
Watabe, K .
ONCOGENE, 2005, 24 (34) :5389-5395
[8]   Mechanism of apoptosis induced by the inhibition of fatty acid synthase in breast cancer cells [J].
Bandyopadhyay, S ;
Zhan, R ;
Wang, Y ;
Pai, SK ;
Hirota, S ;
Hosobe, S ;
Takano, Y ;
Saito, K ;
Furuta, E ;
Iiizumi, M ;
Mohinta, S ;
Watabe, M ;
Chalfant, C ;
Watabe, K .
CANCER RESEARCH, 2006, 66 (11) :5934-5940
[9]   Clinical trial of the pan-caspase inhibitor, IDN-6556, in human liver preservation injury [J].
Baskin-Bey, E. S. ;
Washburn, K. ;
Feng, S. ;
Oltersdorf, T. ;
Shapiro, D. ;
Huyghe, MiRa ;
Burgart, L. ;
Garrity-Park, M. ;
van Vilsteren, F. G. I. ;
Oliver, L. K. ;
Rosen, C. B. ;
Gores, G. J. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2007, 7 (01) :218-225
[10]   ER stress-regulated translation increases tolerance to extreme hypoxia and promotes tumor growth [J].
Bi, MX ;
Naczki, C ;
Koritzinsky, M ;
Fels, D ;
Blais, J ;
Hu, NP ;
Harding, H ;
Novoa, I ;
Varia, M ;
Raleigh, J ;
Scheuner, D ;
Kaufman, RJ ;
Bell, J ;
Ron, D ;
Wouters, BG ;
Koumenis, C .
EMBO JOURNAL, 2005, 24 (19) :3470-3481