A virus causes cancer by inducing massive chromosomal instability through cell fusion

被引:130
作者
Duelli, Dominik M.
Padilla-Nash, Hesed M.
Berman, David
Murphy, Kathleen M.
Ried, Thomas
Lazebnik, Yuri
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] NCI, Genet Branch, NIH, Bethesda, MD 20892 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21231 USA
[4] Johns Hopkins Univ, Sch Med, Mol Diagnost Lab, Baltimore, MD 21287 USA
关键词
D O I
10.1016/j.cub.2007.01.049
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Chromosomal instability (CIN) underlies malignant properties of many solid cancers and their ability to escape therapy, and it might itself cause cancer [1, 2]. CIN is sustained by deficiencies in proteins, such as the tumor suppressor p53 [3-5], that police genome integrity, but the primary cause of CIN in sporadic cancers remains uncertain [6,7]. The primary suspects are mutations that deregulate telomere maintenance, or mitosis, yet such mutations have not been identified in the majority of sporadic cancers [6]. Alternatively, CIN could be caused by a transient event that destabilizes the genome without permanently affecting mechanisms of mitosis or proliferation [5, 8]. Here, we show that an otherwise harmless virus rapidly causes massive chromosomal instability by fusing cells whose cell cycle is deregulated by oncogenes. This synergy between fusion and oncogenes "randomizes" normal diploid human fibroblasts so extensively that each analyzed cell has a unique karyotype, and some produce aggressive, highly aneuploid, heterogeneous, and transplantable epithelial cancers in mice. Because many viruses are fusogenic, this study suggests that viruses, including those that have not been linked to carcinogenesis, can cause chromosomal instability and, consequently, cancer by fusing cells.
引用
收藏
页码:431 / 437
页数:7
相关论文
共 25 条
[1]
Osteoclast nuclei of myeloma patients show chromosome translocations specific for the myeloma cell clone:: a new type of cancer-host partnership? [J].
Andersen, T. L. ;
Boissy, P. ;
Sondergaard, T. E. ;
Kupisiewicz, K. ;
Plesner, T. ;
Rasmussen, T. ;
Haaber, J. ;
Kolvraa, S. ;
Delaisse, J-M .
JOURNAL OF PATHOLOGY, 2007, 211 (01) :10-17
[2]
Syncytin is involved in breast cancer-endothelial cell fusions [J].
Bjerregaard, B. ;
Holck, S. ;
Christensen, I. J. ;
Larsson, L. -I. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2006, 63 (16) :1906-1911
[3]
Unveiling the mechanisms of cell-cell fusion [J].
Chen, EH ;
Olson, EN .
SCIENCE, 2005, 308 (5720) :369-373
[4]
Cell fusion: A hidden enemy? [J].
Duelli, D ;
Lazebnik, Y .
CANCER CELL, 2003, 3 (05) :445-448
[5]
A primate virus generates transformed human cells by fusion [J].
Duelli, DM ;
Hearn, S ;
Myers, MP ;
Lazebnik, Y .
JOURNAL OF CELL BIOLOGY, 2005, 171 (03) :493-503
[6]
Primary cells suppress oncogene-dependent apoptosis [J].
Duelli, DM ;
Lazebnik, YA .
NATURE CELL BIOLOGY, 2000, 2 (11) :859-862
[7]
Duesberg P, 2005, CELL ONCOL, V27, P293
[8]
Cytokinesis failure generating tetraploids promotes tumorigenesis in p53-null cells [J].
Fujiwara, T ;
Bandi, M ;
Nitta, M ;
Ivanova, EV ;
Bronson, RT ;
Pellman, D .
NATURE, 2005, 437 (7061) :1043-1047
[9]
Heim S., 2015, CANC CYTOGENETICS
[10]
Spontaneous fusion with, and transformation of mouse stroma by, malignant human breast cancer epithelium [J].
Jacobsen, Britta M. ;
Harrell, J. Chuck ;
Jedlicka, Paul ;
Borges, Virginia F. ;
Varella-Garcia, Marileila ;
Horwitz, Kathryn B. .
CANCER RESEARCH, 2006, 66 (16) :8274-8279