Abstract 7696: Quantitative plasma proteomics on stellar MS enables discovery of clinically relevant cancer biomarkers

Abstract Quantitative plasma proteomics is essential for discovering circulating biomarkers that enable early cancer detection and patient stratification. However, existing assays often lack the scalability, reproducibility, and sensitivity required for large clinical studies. To overcome these limitations, we developed a high-throughput targeted proteomics workflow on the Thermo Scientific™ Stellar™ mass spectrometer, enabling rapid and precise quantification of plasma proteins. The platform’s fast acquisition speed and robust retention time stability allow comprehensive analysis of hundreds of peptides within a 30-minute gradient, while MS3 fragmentation enhances selectivity for low-abundance targets. Using the Biognosys PQ500 reference peptide kit, we quantified 804 peptides representing 322 plasma proteins, including 57 FDA-approved biomarkers, in plasma from patients with colorectal and lung cancer and healthy donors. More than 94% of peptides showed coefficients of variation below 25%, with linear responses across six orders of magnitude and limits of quantitation down to the attomole range. In colorectal cancer plasma, 29 proteins were significantly altered (adjusted p < 0.05, > 2-fold change) compared with controls. Notably, serum amyloid A2 (SAA2), alpha-2-glycoprotein-like (A2GL), and complement component C9 (CO9) were elevated—proteins implicated in inflammatory and immune pathways driving tumor progression. This study demonstrates that quantitative plasma proteomics on Stellar MS provides the sensitivity, reproducibility, and throughput needed to identify clinically relevant biomarker signatures in cancer. The workflow offers a robust and scalable foundation for translational proteomics and precision oncology applications, bridging the gap between discovery and clinical validation. Citation Format: Stephanie Samra, Qingling Li, Cristina Jacob, Philip Remes, Jared Deyarmin. Quantitative plasma proteomics on stellar MS enables discovery of clinically relevant cancer biomarkers [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 7696.

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Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-7696
Primary Topic
Advanced Proteomics Techniques and Applications
Type
article
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article

Abstract 7696: Quantitative plasma proteomics on stellar MS enables discovery of clinically relevant cancer biomarkers

Philip M. Remes, Jared Deyarmin, Saad Rabie Samra, Qingling Li et al.
Cancer Research
Advanced Proteomics Techniques and Applications
article

Abstract 7696: Quantitative plasma proteomics on stellar MS enables discovery of clinically relevant cancer biomarkers

Philip M. Remes, Jared Deyarmin, Saad Rabie Samra, Qingling Li, Cristina Jacob
article en

Abstract

Abstract Quantitative plasma proteomics is essential for discovering circulating biomarkers that enable early cancer detection and patient stratification. However, existing assays often lack the scalability, reproducibility, and sensitivity required for large clinical studies. To overcome these limitations, we developed a high-throughput targeted proteomics workflow on the Thermo Scientific™ Stellar™ mass spectrometer, enabling rapid and precise quantification of plasma proteins. The platform’s fast acquisition speed and robust retention time stability allow comprehensive analysis of hundreds of peptides within a 30-minute gradient, while MS3 fragmentation enhances selectivity for low-abundance targets. Using the Biognosys PQ500 reference peptide kit, we quantified 804 peptides representing 322 plasma proteins, including 57 FDA-approved biomarkers, in plasma from patients with colorectal and lung cancer and healthy donors. More than 94% of peptides showed coefficients of variation below 25%, with linear responses across six orders of magnitude and limits of quantitation down to the attomole range. In colorectal cancer plasma, 29 proteins were significantly altered (adjusted p < 0.05, > 2-fold change) compared with controls. Notably, serum amyloid A2 (SAA2), alpha-2-glycoprotein-like (A2GL), and complement component C9 (CO9) were elevated—proteins implicated in inflammatory and immune pathways driving tumor progression. This study demonstrates that quantitative plasma proteomics on Stellar MS provides the sensitivity, reproducibility, and throughput needed to identify clinically relevant biomarker signatures in cancer. The workflow offers a robust and scalable foundation for translational proteomics and precision oncology applications, bridging the gap between discovery and clinical validation. Citation Format: Stephanie Samra, Qingling Li, Cristina Jacob, Philip Remes, Jared Deyarmin. Quantitative plasma proteomics on stellar MS enables discovery of clinically relevant cancer biomarkers [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 7696.

Cancer ResearchVol. 86(7_Supplement)
Thermo Fisher Scientific (United States) (US)
Openalex Percentile: Top 6%
Advanced Proteomics Techniques and Applications
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