Haem: Acute Leukaemia Flashcards
Which cell level does CML tend to occur in?
Pluripotent haematopoietic stem cell
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Which cell level does AML tend to occur in?
Pluripotent haematopoietic stem cell or multipotent myeloid stem cell
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List some types of chromosomal abnormalities that are associated with AML.
- Duplications
- Loss
- Translocation
- Inversion
- Deletion
How can altered DNA sequence lead to leukaemia?
- By the creation of a fusion gene
- By abnormal regulation of genes
Which chromosomal duplications are most commonly associated with AML?
8 and 21 (there is a predisposition seen in Down syndrome)
List some molecular abnormalities that an occur in apparently normal chromosomes.
- Point mutations
- Loss of function of tumour suppressor genes
- Partial duplication
- Cryptic deletion (formation of a fusion gene by deletion of a small section of DNA)
List some risk factors for AML.
- Familial
- Constitutional (e.g. Down syndrome)
- Anti-cancer drugs
- Irradiation
- Smoking
What are type 1 and type 2 abnormalities with regards to leukaemogenesis?
- Type 1: promote proliferation and survival (anti-apoptosis)
- Type 2: block differentation
NOTE: leukaemogenesis in AML requires multiple genetic hits
What is the main role of transcription factors?
- They bind to DNA, alter the structure to favour transcription and, ultimately, regulate gene expression
- Disruption of transcription factors can result in failure of differentiation
Give an example of how disruption of a transcription factor can lead to leukaemogenesis.
- Core binding factor (CBF) is the master controller of haemopoiesis
- Translocation 8;21 fuses RUNX1 leading to the formation of a fusion gene that drives leukaemia
- The fusion transcription factor binds to co-repressors leading to a differentiation block
- Inversion of chromosome 16 also affects CBF in a similar way
Which chromosomal aberration causes APML?
Translocation 15;17
What is a characteristic feature of APML? Why does this occur?
- Haemorrhage - this is because APML is associated with DIC and hyperactive fibrinolysis
Name the fusion gene that is responsible for APML.
PML-RARA
In what way are the promyelocytes in APML considered ‘abnormal’?
They contain multiple Auer rods
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Describe how the variant version of APML is different from the original version.
- The variant form has granules that are below the resolution of a light microscope
- They also tend to have bilobed nuclei