# Half the Chromosome It Used to Be: Identifying Cancer Treatments Targeting Aneuploid Losses

## TL;DR

This study identifies cancer treatments that target aneuploid losses, using large datasets to find drug associations with improved survival and cell viability.

## Contribution

The study integrates TCGA and PRISM data to systematically identify treatment strategies for aneuploid cancers.

## Key findings

- 37,720 associations link aneuploidies and treatments with prognosis or cell viability.
- 22 treatments improved 5-year survival for specific aneuploid cancers.
- Glucocorticoid receptor agonists showed selective viability reduction in aneuploid cells.

## Abstract

Background/Objectives: Aneuploidy is near-ubiquitous in cancer and can decrease chemotherapy efficacy while also sensitizing cells to other drugs. Methods: To systematically identify treatment strategies that target aneuploid cancers, data were integrated from The Cancer Genome Atlas (TCGA; 10,967 samples, 16,948 aneuploidy events) and the Broad Institute’s Profiling Relative Inhibition Simultaneously in Mixtures (PRISM) screen of 578 cancer cell lines and 4518 compounds. Results: Our analyses uncovered 37,720 significant positive and negative associations linking specific aneuploidies and treatments with patient prognosis or cell viability. Within TCGA data, 22 treatments correlated with improved 5-year survival for specific aneuploid cancers, whereas 46 were linked to worse outcomes. A complementary analysis of PRISM identified 17,946 compound–aneuploidy associations and 16,189 mechanism of action (MOA)–aneuploidy associations. Pathway-altering compounds that selectively reduce viability in cells with aneuploidy profiles were discovered, including an unexpectedly prominent number of glucocorticoid receptor agonists. Conclusions: This integrated dataset provides a resource for designing therapeutic decision hypotheses, identifying drug-repurposing opportunities, and informing future studies aimed at targeting aneuploidy-induced vulnerabilities in cancer.