Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma.
Floris FoijerLee A AlbackerBjorn BakkerDiana C SpieringsYing YueStephanie Z XieStephanie DavisAnnegret Lutum-JehleDarin TakemotoBrian HareBrinley FureyRoderick T BronsonPeter M LansdorpAllan BradleyPeter K SorgerPublished in: eLife (2017)
Chromosome instability (CIN) is deleterious to normal cells because of the burden of aneuploidy. However, most human solid tumors have an abnormal karyotype implying that gain and loss of chromosomes by cancer cells confers a selective advantage. CIN can be induced in the mouse by inactivating the spindle assembly checkpoint. This is lethal in the germline but we show here that adult T cells and hepatocytes can survive conditional inactivation of the Mad2l1 SAC gene and resulting CIN. This causes rapid onset of acute lymphoblastic leukemia (T-ALL) and progressive development of hepatocellular carcinoma (HCC), both lethal diseases. The resulting DNA copy number variation and patterns of chromosome loss and gain are tumor-type specific, suggesting differential selective pressures on the two tumor cell types.
Keyphrases
- copy number
- mitochondrial dna
- acute lymphoblastic leukemia
- genome wide
- dna damage
- endothelial cells
- drug induced
- cell cycle
- induced apoptosis
- dna methylation
- high glucose
- liver injury
- single cell
- liver failure
- mouse model
- multiple sclerosis
- cell cycle arrest
- diabetic rats
- dna repair
- oxidative stress
- single molecule
- cell therapy
- cell death
- circulating tumor
- cell free
- respiratory failure
- stem cells
- endoplasmic reticulum stress
- induced pluripotent stem cells
- hepatitis b virus
- gene expression
- signaling pathway
- extracorporeal membrane oxygenation
- cell proliferation
- loop mediated isothermal amplification
- young adults
- pluripotent stem cells
- aortic dissection
- acute respiratory distress syndrome
- quantum dots
- genome wide identification
- sensitive detection