Centrosome amplification, chromosomal instability and cancer: mechanistic, clinical and therapeutic issues

被引:50
作者
Cosenza, Marco Raffaele [1 ,2 ]
Kraemer, Alwin [1 ,2 ]
机构
[1] Heidelberg Univ, Clin Cooperat Unit, German Canc Res Ctr DKFZ, Mol Hematol Oncol, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[2] Heidelberg Univ, Dept Internal Med 5, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
关键词
Aneuploidy; Centrosome; Chromosomal instability; ACUTE MYELOID-LEUKEMIA; HUMAN-PAPILLOMAVIRUS TYPE-16; UBIQUITIN-CONJUGATING ENZYME; DETECTABLE CLONAL MOSAICISM; ACTIVATED PROTEIN-KINASE; INTEGRIN-LINKED KINASE; COPY-NUMBER ALTERATION; CELL-CYCLE CHECKPOINT; MAMMALIAN-CELLS; DNA-DAMAGE;
D O I
10.1007/s10577-015-9505-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Centrosomes, the main microtubule-organizing centers in most animal cells, are of crucial importance for the assembly of a bipolar mitotic spindle and subsequent faithful segregation of chromosomes into two daughter cells. Centrosome abnormalities can be found in virtually all cancer types and have been linked to chromosomal instability (CIN) and tumorigenesis. Although our knowledge on centrosome structure, replication, and amplification has greatly increased within recent years, still only very little is known on nature, causes, and consequences of centrosome aberrations in primary tumor tissues. In this review, we summarize our current insights into the mechanistic link between centrosome aberrations, aneuploidy, CIN and tumorigenesis. Mechanisms of induction and cellular consequences of aneuploidy, tetraploidization and CIN, as well as origin and effects of supernumerary centrosomes will be discussed. In addition, animal models for both CIN and centrosome amplification will be outlined. Finally, we describe approaches to exploit centrosome amplification, aneuploidy and CIN for novel and specific anticancer treatment strategies based on the modulation of chromosome missegregation rates.
引用
收藏
页码:105 / 126
页数:22
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