Abstract

“Double-hit” lymphoma (DHL) is a high-grade B-cell lymphoma that harbors concurrent MYC and BCL2 or BCL6 rearrangements. Because cases of MYC/BCL6 DHL are uncommon, most reported conclusions have been based on cases of MYC/BCL2 DHL. Lack of experimental MYC/BCL6 DHL models continues to hinder the pathophysiologic and therapeutic investigations of this disorder. We herein describe a novel MYC/BCL6 DHL cell line, designated DH-My6, carrying both the MYC–IGH and BCL6–IGH fusion genes. Interruptions of MYC and BCL6 expressions using short interfering RNAs and chemical inhibitors led to significant attenuation of DH-My6 cell growth. Greater antitumor effects were found when the cells were treated with a combination of MYC and BCL6 inhibitors. Moreover, the PLK1 inhibitor volasertib and the HDAC inhibitor vorinostat synergized strongly when combined with the bromodomain inhibitor JQ1. DH-My6 is a new well-validated MYC/BCL6 DHL cell line that will provide a useful model for studies of the pathogenesis and therapeutics for the less common DHL tumor type. The rationale for approaches targeting both MYC and BCL6, and in combination with PLK1 or HDAC inhibitors for superior suppression of the aggressive MYC/BCL6 DHL warrants further in vivo testing in a preclinical model.

Highlights

  • “Double-hit” lymphoma (DHL) represents a subset of B-cell malignancies characterized by the presence of MYC (8q24) rearrangement and concurrent

  • We evaluated the potential of MYC- and BCL6-targeted strategies in combination with agents targeting molecules associated with cell proliferation, such as polo-like kinase 1 (PLK1) and histone deacetylase (HDAC) inhibitors, as possible therapeutic approaches to aggressive MYC/BCL6 double-hit lymphoma (DHL)

  • MYC/BCL6 DHL cases make up only 8% of all DHL/triple-hit” lymphoma (THL) cases [1, 4]

Read more

Summary

Introduction

“Double-hit” lymphoma (DHL) represents a subset of B-cell malignancies characterized by the presence of MYC (8q24) rearrangement and concurrent. There have been various lymphoma cell lines that appear to have both MYC and BCL2 rearrangements [12,13,14] Most of these cell lines were reported primarily before sufficient recognition of the clinical importance of DHL and have contributed to the study of lymphomas bearing alterations of both MYC and BCL2. They have not been well authenticated genetically against primary lymphoma cells. We evaluated the potential of MYC- and BCL6-targeted strategies in combination with agents targeting molecules associated with cell proliferation, such as polo-like kinase 1 (PLK1) and histone deacetylase (HDAC) inhibitors, as possible therapeutic approaches to aggressive MYC/BCL6 DHL

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call