Targeting autophagy as a potential therapeutic approach for melanoma therapy

被引:91
作者
Liu, He [1 ]
He, Zhaoyue [1 ]
Simon, Hans-Uwe [1 ]
机构
[1] Univ Bern, Inst Pharmacol, CH-3010 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
Autophagy; Chemotherapy; Hypoxia; Immunotherapy; Melanoma; HLA CLASS-I; CELL-DEATH; ENDOPLASMIC-RETICULUM; REGULATES AUTOPHAGY; CROSS-PRESENTATION; CHROMOSOME; 17Q; APOPTOSIS; INHIBITION; MECHANISM; HYPOXIA;
D O I
10.1016/j.semcancer.2013.06.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Melanoma, occurring as a rapidly progressive skin cancer, is resistant to current chemo- and radiotherapy, especially after metastases to distant organs has taken place. Most chemotherapeutic drugs exert their cytotoxic effect by inducing apoptosis, which, however, is often deficient in cancer cells. Thus, it is appropriate to attempt the targeting of alternative pathways, which regulate cellular viability. Recent studies of autophagy, a well-conserved cellular catabolic process, promise to improve the therapeutic outcome in melanoma patients. Although a dual role for autophagy in cancer therapy has been reported, both protecting against and promoting cell death, the potential for using autophagy in cancer therapy seems to be promising. Here, we review the recent literature on the role of autophagy in melanoma with respect to the expression of autophagic markers, the involvement of autophagy in chemo- and immunotherapy, as well as the role of autophagy in hypoxia and altered metabolic pathways employed for melanoma therapy. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:352 / 360
页数:9
相关论文
共 88 条
[11]   G-quadruplexes: targets and tools in anticancer drug design [J].
Duechler, Markus .
JOURNAL OF DRUG TARGETING, 2012, 20 (05) :389-400
[12]   Discovery and characterization of a second mammalian thiol dioxygenase, cysteamine dioxygenase [J].
E. Dominy, John, Jr. ;
Simmons, Chad R. ;
Hirschberger, Lawrence L. ;
Hwang, Jesse ;
Coloso, Relicardo M. ;
Stipanuk, Martha H. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (35) :25189-25198
[13]   Hypoxia Negatively Regulates Antimetastatic PEDF in Melanoma Cells by a Hypoxia Inducible Factor-Independent, Autophagy Dependent Mechanism [J].
Fernandez-Barral, Asuncion ;
Luis Orgaz, Jose ;
Gomez, Valenti ;
del Peso, Luis ;
Jose Calzada, Maria ;
Jimenez, Benilde .
PLOS ONE, 2012, 7 (03)
[14]   Improved Survival with MEK Inhibition in BRAF-Mutated Melanoma [J].
Flaherty, Keith T. ;
Robert, Caroline ;
Hersey, Peter ;
Nathan, Paul ;
Garbe, Claus ;
Milhem, Mohammed ;
Demidov, Lev V. ;
Hassel, Jessica C. ;
Rutkowski, Piotr ;
Mohr, Peter ;
Dummer, Reinhard ;
Trefzer, Uwe ;
Larkin, James M. G. ;
Utikal, Jochen ;
Dreno, Brigitte ;
Nyakas, Marta ;
Middleton, Mark R. ;
Becker, Juergen C. ;
Casey, Michelle ;
Sherman, Laurie J. ;
Wu, Frank S. ;
Ouellet, Daniele ;
Martin, Anne-Marie ;
Patel, Kiran ;
Schadendorf, Dirk .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (02) :107-114
[15]  
GAO X, 1995, CANCER RES, V55, P1002
[16]   Autophagy and hypoxia in colonic adenomas related to aggressive features [J].
Giatromanolaki, A. ;
Koukourakis, M. I. ;
Koutsopoulos, A. V. ;
Harris, A. L. ;
Gatter, K. C. ;
Sivridis, E. .
COLORECTAL DISEASE, 2013, 15 (05) :E223-E230
[17]   Autophagy as a cell death and tumor suppressor mechanism [J].
Gozuacik, D ;
Kimchi, A .
ONCOGENE, 2004, 23 (16) :2891-2906
[18]   Defining the role of mTOR in cancer [J].
Guertin, David A. ;
Sabatini, David M. .
CANCER CELL, 2007, 12 (01) :9-22
[19]   Necroptosis modulated by autophagy is a predominant form of melanoma cell death induced by sanguilutine [J].
Hammerova, Jindriska ;
Uldrijan, Stjepan ;
Taborska, Eva ;
Vaculova, Alena Hyrslova ;
Slaninova, Iva .
BIOLOGICAL CHEMISTRY, 2012, 393 (07) :647-658
[20]   Overexpression of autophagy-related beclin-1 in advanced malignant melanoma and its low expression in melanoma-in-situ [J].
Hara, Yoko ;
Nakamura, Motonobu .
EUROPEAN JOURNAL OF DERMATOLOGY, 2012, 22 (01) :128-129