Abstract
ABStRACt Although the study of leukemogenesis has traditionally focused on protein-coding genes, the role of enhancer dysregulation is becoming increasingly recognized. The advent of high-throughput sequencing, together with a better understanding of enhancer biology, has revealed how various genetic and epigenetic lesions produce oncogenic enhancers that drive transformation. These aberrations include translocations that lead to enhancer hijacking, point mutations that modulate enhancer activity, and copy number alterations that modify enhancer dosage. In this review, we describe these mechanisms in the context of leukemia and discuss potential therapeutic avenues to target these regulatory elements.
| Original language | English |
|---|---|
| Pages (from-to) | 303-317 |
| Number of pages | 15 |
| Journal | Blood cancer discovery |
| Volume | 5 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 3 Sept 2024 |
Bibliographical note
Publisher Copyright:©2024 American Association for Cancer Research.