Mitotic cell death by chromosome fragmentation

被引:70
作者
Stevens, Joshua B.
Liu, Guo
Bremer, Steven W.
Ye, Karen J.
Xu, Wenxin
Xu, Jing
Sun, Yi
Wu, Gen Sheng
Savasan, Sureyya
Krawetz, Stephen A.
Ye, Christine J.
Heng, Henry H. Q.
机构
[1] Wayne State Univ, Sch Med, Ctr Mol Med & Genet, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Dept Pathol, Detroit, MI 48201 USA
[3] Wayne State Univ, Sch Med, Karmanos Canc Inst, Detroit, MI 48201 USA
[4] SeeDNA Biotech Inc, Windsor, ON, Canada
[5] Univ Michigan, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
关键词
D O I
10.1158/0008-5472.CAN-07-0472
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cell death plays a key role for both cancer progression and treatment. In this report, we characterize chromosome fragmentation, a new type of cell death that takes place during metaphase where condensed chromosomes are progressively degraded. It occurs spontaneously without any treatment in instances such as inherited status of genomic instability, or it can be induced by treatment with chemotherapeutics. It is observed within cell lines, tumors, and lymphocytes of cancer patients. The process of chromosome fragmentation results in loss of viability, but is apparently nonapoptotic and further differs from cellular death defined by mitotic catastrophe. Chromosome fragmentation represents an efficient means of induced cell death and is a clinically relevant biomarker of mitotic cell death. Chromosome fragmentation serves as a method to eliminate genomically unstable cells. Paradoxically, this process could result in genome aberrations common in cancer. The characterization of chromosome fragmentation may also shine light on the mechanism of chromosomal pulverization.
引用
收藏
页码:7686 / 7694
页数:9
相关论文
共 44 条
[1]  
Andreassen PR, 2001, CANCER RES, V61, P7660
[2]  
BARLOGIE B, 1976, CANCER RES, V36, P1975
[3]  
Brown EJ, 2000, GENE DEV, V14, P397
[4]   Mitotic catastrophe constitutes a special case of apoptosis whose suppression entails aneuploidy [J].
Castedo, M ;
Perfettini, JL ;
Roumier, T ;
Valent, A ;
Raslova, H ;
Yakushijin, K ;
Horne, D ;
Feunteun, J ;
Lenoir, G ;
Medema, R ;
Vainchenker, W ;
Kroemer, G .
ONCOGENE, 2004, 23 (25) :4362-4370
[5]   Cell death by mitotic catastrophe: a molecular definition [J].
Castedo, M ;
Perfettini, JL ;
Roumie, T ;
Andreau, K ;
Medema, R ;
Kroemer, G .
ONCOGENE, 2004, 23 (16) :2825-2837
[6]   Neoadjuvant concurrent paclitaxel and radiation in stage II/III breast cancer [J].
Chakravarthy, AB ;
Kelley, MC ;
McLaren, B ;
Truica, CI ;
Billheimer, D ;
Mayer, IA ;
Grau, AM ;
Johnson, DH ;
Simpson, JF ;
Beauchamp, RD ;
Jones, C ;
Pietenpol, JA .
CLINICAL CANCER RESEARCH, 2006, 12 (05) :1570-1576
[7]   14-3-3σ is required to prevent mitotic catastrophe after DNA damage [J].
Chan, TA ;
Hermeking, H ;
Lengauer, C ;
Kinzler, KW ;
Vogelstein, B .
NATURE, 1999, 401 (6753) :616-620
[8]   Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sites [J].
Durkin, S. G. ;
Arlt, M. F. ;
Howlett, N. G. ;
Glover, T. W. .
ONCOGENE, 2006, 25 (32) :4381-4388
[9]   Expression of Bcl-2 in human epithelial tumor (HeLa) cells enhances clonogenic survival following exposure to 5-fluoro-2′-deoxyuridine or staurosporine, but not following exposure to etoposide or doxorubicin [J].
Elliott, MJ ;
Stribinskiene, L ;
Lock, RB .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1998, 41 (06) :457-463
[10]   Genomic instability and apoptosis are frequent in p53 deficient young mice [J].
Fukasawa, K ;
Wiener, F ;
VandeWoude, GF ;
Mai, SB .
ONCOGENE, 1997, 15 (11) :1295-1302