Serine metabolism is essential for leukemogenesis and stemness in acute myeloid leukemia (AML). Here the authors show that targeting IGF2BP3 disrupts the serine synthesis pathway in AML cells in an RNA N6-Methyladenosine modification dependent manner, sensitizing AML cells to serine and glycine deprivation.
- Feng Huang
- Yushuai Wang
- Hengyou Weng