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From the book Polyploidization and Cancer

Polyploidy, Aneuploidy and the Evolution of Cancer

Lauren M. F. Merlo, Li-san Wang, John W. Pepper, Peter S. Rabinovitch and Carlo C. Maley

Most cancers cells are aneuploid, meaning they contain the wrong number of chromosomes. Aneuploidy entails the loss or gain of individual chromosomes or large sections of chromosomes and is defined here as distinct from polyploidy, which involves extra copies of the entire genome, such as triploidy (3N) or tetraploidy (4N). Large‑scale chromosomal amplifications and deletions in cancers have been demonstrated using a variety of methods, including comparative genomic hybridization (CGH), karyotyping and fluorescence in situ hybridization (FISH). The frequency with which aneuploidy is observed in cancer leads to a series of important questions: How do cancers become aneuploid? What genes are being targeted by the amplifications and deletions? How can cells survive with such massive perturbations to their genomes? How has the selective pressure of cancer shaped our genomes to sense and respond to these perturbations? Most of these questions have received little attention to date and the answers remain largely unknown. To facilitate research on these questions, we review what is known about each in an effort to frame the questions and hypotheses more precisely and propose methods that might be used to reach an answer.

Taken from the book

Polyploidization and Cancer

Edited by: Randy Y.C. Poon

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