Abstract 3414: PDO as Translational Model for Biomarker Discovery in NSCLC

Abstract This study leverages treatment-naïve patient-derived organoids (PDOs) as a powerful translational model to drive biomarker discovery in non-small cell lung cancer (NSCLC). Current biomarker discovery efforts rely predominantly on publicly available datasets that predict cell surface localization at the RNA level. By focusing on the proteomic characterization of the cell surface, specifically targeting N-glycosylated proteins, we aim to capture the dynamic landscape of membrane proteins that play key roles in tumor biology.We performed a surfaceome screening on a cohort of 15 NSCLC organoids and 5 matched normal lung organoids after in vitro treatment with saline, cisplatin and B7H3 ADC. Live-cell biotin labeling followed by enrichment enabled isolation of glycosylated cell surface proteins. Downstream LC-MS/MS-based proteomics allowed quantitative profiling of both enriched and total protein fractions. Concurrently, transcriptomic profiling via RNA-seq and WGS will enable cross-comparative analysis. This proteogenomic approach will be critical given that transcript-level data do not always reflect actual protein expression, particularly for membrane proteins that may be subject to complex post-translational modifications and regulation. Comprehensive multiomic in silico analyses are currently ongoing to integrate our experimental data with external databases, including CPTAC, TCGA, TEMPUS, and GTEx. These computational analyses are designed to refine our list of candidate biomarkers based on high protein expression and differential expression pre- and post-treatment.Our approach underscores the potential of utilizing advanced proteomic and transcriptomic methodologies in tandem with cutting-edge in silico analyses to better understand tumor biology. Further analysis and validation studies will be needed to ensure that the biomarkers we identify have the highest translational potential and can be used as effective diagnostic tools. Citation Format: Maria C. Speranza, Anna Pasto, Halh Al-Serori, Elisavet Chatzopoulou, Veronika Yankova, Henrik Hammarén, Patricia Sauer, Kathrin Uhrig, Helena Rannikmae, Lena Eismann, Edward Curry, Tony NG, Kenneth W. Hance. PDO as Translational Model for Biomarker Discovery in NSCLC [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3414.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-3414
Primary Topic
Advanced Proteomics Techniques and Applications
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article
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article

Abstract 3414: PDO as Translational Model for Biomarker Discovery in NSCLC

Kenneth W. Hance, Maria C. Speranza, Tony Ng, Helena Rannikmäe et al.
Cancer Research
Advanced Proteomics Techniques and Applications
article

Abstract 3414: PDO as Translational Model for Biomarker Discovery in NSCLC

Kenneth W. Hance, Maria C. Speranza, Tony Ng, Helena Rannikmäe, Lena Eismann, Anna Pastò, Edward Curry, Elisavet I. Chatzopoulou, Patricia Sauer, Henrik M. Hammarén, Halh Al-Serori, Veronika Yankova, Kathrin Uhrig
article en

Abstract

Abstract This study leverages treatment-naïve patient-derived organoids (PDOs) as a powerful translational model to drive biomarker discovery in non-small cell lung cancer (NSCLC). Current biomarker discovery efforts rely predominantly on publicly available datasets that predict cell surface localization at the RNA level. By focusing on the proteomic characterization of the cell surface, specifically targeting N-glycosylated proteins, we aim to capture the dynamic landscape of membrane proteins that play key roles in tumor biology.We performed a surfaceome screening on a cohort of 15 NSCLC organoids and 5 matched normal lung organoids after in vitro treatment with saline, cisplatin and B7H3 ADC. Live-cell biotin labeling followed by enrichment enabled isolation of glycosylated cell surface proteins. Downstream LC-MS/MS-based proteomics allowed quantitative profiling of both enriched and total protein fractions. Concurrently, transcriptomic profiling via RNA-seq and WGS will enable cross-comparative analysis. This proteogenomic approach will be critical given that transcript-level data do not always reflect actual protein expression, particularly for membrane proteins that may be subject to complex post-translational modifications and regulation. Comprehensive multiomic in silico analyses are currently ongoing to integrate our experimental data with external databases, including CPTAC, TCGA, TEMPUS, and GTEx. These computational analyses are designed to refine our list of candidate biomarkers based on high protein expression and differential expression pre- and post-treatment.Our approach underscores the potential of utilizing advanced proteomic and transcriptomic methodologies in tandem with cutting-edge in silico analyses to better understand tumor biology. Further analysis and validation studies will be needed to ensure that the biomarkers we identify have the highest translational potential and can be used as effective diagnostic tools. Citation Format: Maria C. Speranza, Anna Pasto, Halh Al-Serori, Elisavet Chatzopoulou, Veronika Yankova, Henrik Hammarén, Patricia Sauer, Kathrin Uhrig, Helena Rannikmae, Lena Eismann, Edward Curry, Tony NG, Kenneth W. Hance. PDO as Translational Model for Biomarker Discovery in NSCLC [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3414.

Cancer ResearchVol. 86(7_Supplement)
GlaxoSmithKline (United Kingdom) (GB), Age UK (GB), GlaxoSmithKline (Germany) (DE)
Good health and well-being
Openalex Percentile: Top 31%
Advanced Proteomics Techniques and Applications
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