DNA damage and the balance between survival and death in cancer biology

被引:881
作者
Roos, Wynand P. [1 ]
Thomas, Adam D. [1 ]
Kaina, Bernd [1 ]
机构
[1] Univ Med Ctr, Inst Toxicol, Obere Zahlbacher Str 67, D-55131 Mainz, Germany
关键词
RECEPTOR-INTERACTING PROTEIN; MALIGNANT GLIOMA-CELLS; TRANSCRIPTION COUPLED REPAIR; NUCLEOTIDE EXCISION-REPAIR; P53; TUMOR-SUPPRESSOR; EMBRYONIC STEM-CELLS; STRAND BREAK REPAIR; ANTI-APOPTOSIS GENE; KAPPA-B ACTIVATION; C-FOS;
D O I
10.1038/nrc.2015.2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA is vulnerable to damage resulting from endogenous metabolites, environmental and dietary carcinogens, some anti-inflammatory drugs, and genotoxic cancer therapeutics. Cells respond to DNA damage by activating complex signalling networks that decide cell fate, promoting not only DNA repair and survival but also cell death. The decision between cell survival and death following DNA damage rests on factors that are involved in DNA damage recognition, and DNA repair and damage tolerance, as well as on factors involved in the activation of apoptosis, necrosis, autophagy and senescence. The pathways that dictate cell fate are entwined and have key roles in cancer initiation and progression. Furthermore, they determine the outcome of cancer therapy with genotoxic drugs. Understanding the molecular basis of these pathways is important not only for gaining insight into carcinogenesis, but also in promoting successful cancer therapy. In this Review, we describe key decision-making nodes in the complex interplay between cell survival and death following DNA damage.
引用
收藏
页码:20 / 33
页数:14
相关论文
共 197 条
[1]  
Adida C, 1998, AM J PATHOL, V152, P43
[2]   ATM engages the TSC2/mTORC1 signaling node to regulate autophagy [J].
Alexander, Angela ;
Kim, Jinhee ;
Walker, Cheryl L. .
AUTOPHAGY, 2010, 6 (05) :672-673
[3]   ATM signals to TSC2 in the cytoplasm to regulate mTORC1 in response to ROS [J].
Alexander, Angela ;
Cai, Sheng-Li ;
Kim, Jinhee ;
Nanez, Adrian ;
Sahin, Mustafa ;
MacLean, Kirsteen H. ;
Inoki, Ken ;
Guan, Kun-Liang ;
Shen, Jianjun ;
Person, Maria D. ;
Kusewitt, Donna ;
Mills, Gordon B. ;
Kastan, Michael B. ;
Walker, Cheryl Lyn .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (09) :4153-4158
[4]   Survivin and IAP proteins in cell-death mechanisms [J].
Altieri, Dario C. .
BIOCHEMICAL JOURNAL, 2010, 430 :199-205
[5]   A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma [J].
Ambrosini, G ;
Adida, C ;
Altieri, DC .
NATURE MEDICINE, 1997, 3 (08) :917-921
[6]   Transcription abnormalities potentiate apoptosis of normal human fibroblasts [J].
Andera, L ;
Wasylyk, B .
MOLECULAR MEDICINE, 1997, 3 (12) :852-863
[7]   PIDD Death-Domain Phosphorylation by ATM Controls Prodeath versus Prosurvival PIDDosome Signaling [J].
Ando, Kiyohiro ;
Kernan, Jennifer L. ;
Liu, Peter H. ;
Sanda, Takaomi ;
Logette, Emmanuelle ;
Tschopp, Jurg ;
Look, A. Thomas ;
Wang, Jianlong ;
Bouchier-Hayes, Lisa ;
Sidi, Samuel .
MOLECULAR CELL, 2012, 47 (05) :681-693
[8]   Mitochondrial and Nuclear Cross Talk in Cell Death Parthanatos [J].
Andrabi, Shaida A. ;
Dawson, Ted M. ;
Dawson, Valina L. .
MITOCHONDRIA AND OXIDATIVE STRESS IN NEURODEGENERATIVE DISORDERS, 2008, 1147 :233-241
[9]   Topoisomerase-mediated chromosomal break repair: an emerging player in many games [J].
Ashour, Mohamed E. ;
Atteya, Reham ;
El-Khamisy, Sherif F. .
NATURE REVIEWS CANCER, 2015, 15 (03) :137-151
[10]   Malignant melanoma cells acquire resistance to DNA interstrand cross-linking chemotherapeutics by p53-triggered upregulation of DDB2/XPC-mediated DNA repair [J].
Barckhausen, C. ;
Roos, W. P. ;
Naumann, S. C. ;
Kaina, B. .
ONCOGENE, 2014, 33 (15) :1964-1974