Published April 23, 2013 | Version v1

Lenalidomide, p53 and del(5q) Myelodysplastic Syndrome: Ribosome Stress Relief

  • 1. Monter Cancer Center, North Shore-LIJ Cancer Institute, Lake Success, NY 11042, US.
  • 2. Monter Cancer Center, North Shore-LIJ Cancer Institute, Lake Success, NY 11042, US; The Feinstein Institute for Medical Research, Manhasset, NY 11030 US; Hofstra North Shore-LIJ School of Medicine, Hempstead, NY, US.

Description

Whereas deletions involving the long arm of chromosome 5 are among the most common
chromosomal abnormalities in myelodysplastic syndrome (MDS), isolated del(5q) MDS,
which includes the 5q- syndrome, is rare and characterized by hypoplastic anemia and a
moderate risk of transformation to acute myeloid leukemia (AML). The 5q- syndrome is
now recognized as a ribosomopathy, and both the classic 5q- syndrome and del(5q) MDS
are uniquely responsive to lenalidomide. However, the mechanism of action of
lenalidomide is controversial and involves modulation of p53 activity, which may be
beneficial in anemia remission but suggested to lead to malignant cell outgrowth. Here,
we critically review the literature on this important controversy, which has obvious
implications for therapy of del (5q) MDS.

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