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Table 2 Examples of different types of causative factors of aneuploidy

From: Understanding aneuploidy in cancer through the lens of system inheritance, fuzzy inheritance and emergence of new genome systems

1. Gene mutations/epigenetic alterations

[111,112,113]

  Mitotic checkpoint defects, e.g. BUB1, MAD1 and CENPE

[114, 115]

  Microtubule attachment defects, e.g. aurora kinase B, Cydlin A,

 

  Mitotic spindle and centrosome defects

[116]

  Other CIN-related mutation, e.g. p53, ATM

[117]

2. Stress- (physiological, pathological and pharmaceutical) related responses

  Defective mitotic figures (condensation defects) (DMF, sticky chromosomes)

[50, 78, 106]

  Chromosome fragmentations (C-Frags)

[115, 116]

  Genome chaos

[5, 6, 37, 59, 67]

  Chromosomal cycle variations (replication, condensation, segregation, de-condensation)

[104]

  Non-specific stress (triggers type II CIN)

[50]

3. Genome system variability

  Fuzzy inheritance

[4, 37, 59]

  Cellular adaptation

[37, 95]

  Survival under high stress

[56, 67]

  1. To illustrate the viewpoint that many genomic and environmental factors can contribute to aneuploidy, a few examples are presented, among a large number of publications. We focus more on the examples that feature a cytogenetic perspective, as these are currently less popular compared to gene mutation studies, despite their importance