Disharoon Andrew O, Delaney Joe R
Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA.
Genes (Basel). 2025 Jun 14;16(6):708. doi: 10.3390/genes16060708.
BACKGROUND/OBJECTIVES: Aneuploidy is near-ubiquitous in cancer and can decrease chemotherapy efficacy while also sensitizing cells to other drugs.
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.
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.
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.
背景/目的:非整倍体在癌症中几乎普遍存在,它会降低化疗疗效,同时也会使细胞对其他药物敏感。
为了系统地确定针对非整倍体癌症的治疗策略,整合了来自癌症基因组图谱(TCGA;10967个样本,16948个非整倍体事件)以及布罗德研究所对578个癌细胞系和4518种化合物进行的同时混合相对抑制分析(PRISM)筛选的数据。
我们的分析发现了37720个显著的正相关和负相关,这些相关性将特定的非整倍体和治疗方法与患者预后或细胞活力联系起来。在TCGA数据中,22种治疗方法与特定非整倍体癌症患者的5年生存率提高相关,而46种治疗方法与较差的预后相关。对PRISM的补充分析确定了17946个化合物 - 非整倍体关联和16189个作用机制(MOA) - 非整倍体关联。发现了能选择性降低具有非整倍体特征细胞活力的改变通路的化合物,包括数量意外众多的糖皮质激素受体激动剂。
这个整合数据集为设计治疗决策假设、确定药物重新利用机会以及为未来旨在针对癌症中非整倍体诱导的脆弱性的研究提供信息提供了资源。