We present the CellHit web server ( https:// cellhit.bioinfolab.sns.it/ ), a web-based platform designed to predict and analyze cancer patients’ responsiveness to drugs using transcriptomic data. Leveraging extensive pharmacogenomics datasets from the Genomics of Drug Sensitivity in Cancer v1 and v2 (GDSC) and Profiling Relative Inhibition Simultaneously in Mixtures (PRISM) and transcriptomic data from the Cancer Cell Line Encyclopedia (CCLE) and TCGA, CellHit integrates a computational pipeline for preprocessing, gene imputation, and robust alignment between patient and cell line transcriptomic data with pre-trained SOTA models for drug sensitivity prediction. The pipeline employs batch correction, enhanced Celligner methodology, and Parametric UMAP for stable and actionable alignment. The intuitive interface requires no programming expertise, offering interactive visualizations, including low-dimensional embeddings and drug sensitivity heatmaps for the input transcriptomic samples. Results feature contextual metadata, SHAP -based feature importance, and transcriptomic neighbors from reference datasets, simplifying interpretation and hypothesis generation. CellHit provides precomputed predictions across TCGA samples and offers the ability to run custom analyses online on input samples, democratizing precision oncology by enabling rapid, interpretable predictions accessible to a broad research community.

CellHit : a web server to predict and analyze cancer patients’ drug responsiveness

Carli, Francesco
;
De Oliveira Rosa, Natalia
;
Di Chiaro, Pierluigi;Bisceglia, Luisa;Raimondi, Francesco
2025

Abstract

We present the CellHit web server ( https:// cellhit.bioinfolab.sns.it/ ), a web-based platform designed to predict and analyze cancer patients’ responsiveness to drugs using transcriptomic data. Leveraging extensive pharmacogenomics datasets from the Genomics of Drug Sensitivity in Cancer v1 and v2 (GDSC) and Profiling Relative Inhibition Simultaneously in Mixtures (PRISM) and transcriptomic data from the Cancer Cell Line Encyclopedia (CCLE) and TCGA, CellHit integrates a computational pipeline for preprocessing, gene imputation, and robust alignment between patient and cell line transcriptomic data with pre-trained SOTA models for drug sensitivity prediction. The pipeline employs batch correction, enhanced Celligner methodology, and Parametric UMAP for stable and actionable alignment. The intuitive interface requires no programming expertise, offering interactive visualizations, including low-dimensional embeddings and drug sensitivity heatmaps for the input transcriptomic samples. Results feature contextual metadata, SHAP -based feature importance, and transcriptomic neighbors from reference datasets, simplifying interpretation and hypothesis generation. CellHit provides precomputed predictions across TCGA samples and offers the ability to run custom analyses online on input samples, democratizing precision oncology by enabling rapid, interpretable predictions accessible to a broad research community.
2025
Settore BIO/11 - Biologia Molecolare
Settore BIOS-08/A - Biologia molecolare
Drug sensitivity prediction; Transcriptomic data; Precision oncology; Pharmacogenomics; GDSC; PRISM; CCLE; TCGA; Celligner
   Decoding and recoding onco-GPCR signaling through integrative bioinformatics and protein engineering
   ASSOCIAZIONE ITALIANA PER LA RICERCA SUL CANCRO (AIRC)
   MFAG 2020 ID 24317

   Tuscany Health Ecosystem
   THE
   MUR
   PNNR
   ECS_00000017
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11384/153223
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