"Myeloid" Mutations in ALL Are Not Uncommon: Implications for Etiology and Therapies.
Ilaria IacobucciPublished in: Blood cancer discovery (2024)
In Blood Cancer Discovery, Saygin and colleagues report that somatic variants that are recurrent in myeloid malignancies can also occur with high frequency (16%) in adult acute lymphoblastic leukemia (ALL) where they correlate with older age, diagnosis following genotoxic therapy for a prior malignancy and worse outcome to chemotherapy. Mutations in these "myeloid" genes can precede ALL diagnosis and arise in hematopoietic stem or progenitor cells that clonally expand and differentiate into both lymphoblasts and nonmalignant myeloid cells, supporting a role for clonal hematopoiesis as premalignant state outside the context of myeloid malignancies and providing implications for both ALL etiology and therapeutic intervention. See related article by Saygin et al., p. 164 (4).
Keyphrases
- high frequency
- dendritic cells
- bone marrow
- acute myeloid leukemia
- acute lymphoblastic leukemia
- transcranial magnetic stimulation
- copy number
- randomized controlled trial
- physical activity
- gene expression
- papillary thyroid
- genome wide
- cell death
- young adults
- high throughput
- transcription factor
- middle aged
- squamous cell
- locally advanced
- cell proliferation
- rectal cancer
- single cell