Data from Avadomide Induces Degradation of ZMYM2 Fusion Oncoproteins in Hematologic Malignancies

Abstract

<div>Abstract<p>Thalidomide analogues exert their therapeutic effects by binding to the CRL4<sup>CRBN</sup> E3 ubiquitin ligase, promoting ubiquitination and subsequent proteasomal degradation of specific protein substrates. Drug-induced degradation of IKZF1 and IKZF3 in B-cell malignancies demonstrates the clinical utility of targeting disease-relevant transcription factors for degradation. Here, we found that avadomide (CC-122) induces CRBN-dependent ubiquitination and proteasomal degradation of ZMYM2 (ZNF198), a transcription factor involved in balanced chromosomal rearrangements with <i>FGFR1</i> and <i>FLT3</i> in aggressive forms of hematologic malignancies. The minimal drug-responsive element of ZMYM2 is a zinc-chelating MYM domain and is contained in the N-terminal portion of ZMYM2 that is universally included in the derived fusion proteins. We demonstrate that avadomide has the ability to induce proteasomal degradation of ZMYM2–FGFR1 and ZMYM2–FLT3 chimeric oncoproteins, both <i>in vitro</i> and <i>in vivo</i>. Our findings suggest that patients with hematologic malignancies harboring these <i>ZMYM2</i> fusion proteins may benefit from avadomide treatment.</p>Significance:<p>We extend the potential clinical scope of thalidomide analogues by the identification of a novel avadomide-dependent CRL4<sup>CRBN</sup> substrate, ZMYM2. Avadomide induces ubiquitination and degradation of ZMYM2–FGFR1 and ZMYM2–FLT3, two chimeric oncoproteins involved in hematologic malignancies, providing a proof of concept for drug-induced degradation of transcription factor fusion proteins by thalidomide analogues.</p></div>