AUTHOR=Lee Unsun , Szabova Ludmila , Collins Victor J. , Gordon Melanie , Johnson Kristine , Householder Deborah , Jorgensen Stephanie , Lu Lucy , Bassel Laura , Elloumi Fathi , Peer Cody J. , Nelson Ariana E. , Varriano Sophia , Varma Sudhir , Roberts Ryan D. , Ohler Zoe Weaver , Figg William D. , Sharan Shyam K. , Pommier Yves , Heske Christine M. TITLE=Treatment with novel topoisomerase inhibitors in Ewing sarcoma models reveals heterogeneity of tumor response JOURNAL=Frontiers in Cell and Developmental Biology VOLUME=12 YEAR=2024 URL=https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2024.1462840 DOI=10.3389/fcell.2024.1462840 ISSN=2296-634X ABSTRACT=Introduction

The topoisomerase 1 (TOP1) inhibitor irinotecan is a standard-of-care agent for relapsed Ewing sarcoma (EWS), but its efficacy is limited by chemical instability, rapid clearance and reversibility, and dose-limiting toxicities, such as diarrhea. Indenoisoquinolines (IIQs) represent a new class of clinical TOP1 inhibitors designed to address these limitations.

Methods

In this study, we evaluated the preclinical efficacy of three IIQs (LMP400, LMP744, and LMP776) in relevant models of EWS. We characterized the pharmacokinetics of IIQs in orthotopic xenograft models of EWS, optimized the dosing regimen through tolerability studies, and tested the efficacy of IIQs in a panel of six molecularly heterogeneous EWS patient-derived xenograft (PDX) models. For each PDX, we conducted whole genome and RNA sequencing, and methylation analysis.

Results

We show that IIQs potently inhibit the proliferation of EWS cells in vitro, inducing complete cell growth inhibition at nanomolar concentrations via induction of DNA damage and apoptotic cell death. LMP400 treatment induced ≥30% tumor regression in two of six PDX models, with more durable regression compared to irinotecan treatment in one of these models. RNA sequencing of PDX models identified a candidate predictive biomarker gene signature for LMP400 response. These data, along with pharmacogenomic data on IIQs in sarcoma cell lines, are available at a new interactive public website: https://discover.nci.nih.gov/rsconnect/EwingSarcomaMinerCDB/.

Discussion

Our findings suggest that IIQs may be promising new agents for a subset of EWS patients.