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Efficacy of Polo-life kinase 1 inhibitors in preclinical models of small cell lung cancer

GSE269636 Homo sapiens Expression profiling by high throughput sequencing 6 samples Submitted 2025/02/14 Platform GPL24676
Summary
Small cell lung cancer (SCLC) remains a significant health problem with more than 180,000 newly afflicted patients worldwide per year. Recurrence following initial frontline therapy is associated with resistance to salvage treatment and remains the area of greatest unmet need for SCLC patients. This study systematically examined the efficacy of three different polo like kinase 1 (PLK1) inhibitors in preclinical models of SCLC. The study uncovered robust in vitro activity of PLK1 inhibitors against SCLC cell lines and confirmed the efficacy in patient-derived xenograft models of platinum sensitive and resistant SCLC. A known challenge of targeted therapies in the clinic is the inevitable development of resistance and loss of efficacy. Therefore, understanding the potential mechanisms driving acquired resistance could offer additional strategies to enhance efficacy, delay the development of resistance or reverse the resistance. We generated lab-derived resistant SCLC cells by continuous exposure of parental cells to increasing concentration of onvansertib and performed RNA-seq to identify potential resistance mechanisms.
Published in
Polo-like Kinase 1 Inhibitors Demonstrate In Vitro and In Vivo Efficacy in Preclinical Models of Small Cell Lung Cancer
Zhang G, Pannucci A, Ivanov AA et al. · Cancers 2025 · PMID 39941812 · doi:10.3390/cancers17030446
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Direct links to NCBI, no account and no request form: the whole study as GSE269636_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 6 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1122852 and SRA study SRP513300. Searching any of these in the dataset finder brings you back here.

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