Romidepsin targets multiple survival signaling pathways in malignant T cells

• Published in: Blood cancer journal (New York) Vol. 5; no. 10; p. e357
• Main Authors: Valdez, B C, Brammer, J E, Li, Y, Murray, D, Liu, Y, Hosing, C, Nieto, Y, Champlin, R E, Andersson, B S
• Format: Journal Article
• Language: English
• Published: United States Springer Nature B.V 16.10.2015; Nature Publishing Group
• Subjects: Antineoplastic Agents - pharmacology; Blotting, Western; Cell Line, Tumor; Cell Proliferation - drug effects; Cell Survival - drug effects; Depsipeptides - pharmacology; Humans; Lymphoma, T-Cell; Original; Real-Time Polymerase Chain Reaction; Signal Transduction - drug effects
• ISSN: 2044-5385; 2044-5385
• DOI: 10.1038/bcj.2015.83

Romidepsin is a cyclic molecule that inhibits histone deacetylases. It is Food and Drug Administration-approved for treatment of cutaneous and peripheral T-cell lymphoma, but its precise mechanism of action against malignant T cells is unknown. To better understand the biological effects of romidepsin in these cells, we exposed PEER and SUPT1 T-cell lines, and a primary sample from T-cell lymphoma patient (Patient J) to romidepsin. We then examined the consequences in some key oncogenic signaling pathways. Romidepsin displayed IC50 values of 10.8, 7.9 and 7.0 nm in PEER, SUPT1 and Patient J cells, respectively. Strong inhibition of histone deacetylases and demethylases, increased production of reactive oxygen species and decreased mitochondrial membrane potential were observed, which may contribute to the observed DNA-damage response and apoptosis. The stress-activated protein kinase/c-Jun N-terminal kinase signaling pathway and unfolded protein response in the endoplasmic reticulum were activated, whereas the phosphatidylinositol 3-kinase/AKT/mammalian target of rapamycin (PI3K/AKT/mTOR) and β-catenin pro-survival pathways were inhibited. The decreased level of β-catenin correlated with the upregulation of its inhibitor SFRP1 through romidepsin-mediated hypomethylation of its gene promoter. Our results provide new insights into how romidepsin invokes malignant T-cell killing, show evidence of its associated DNA hypomethylating activity and offer a rationale for the development of romidepsin-containing combination therapies.