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April 5, 2026Cancer Research0 citations

Abstract 726: Engineered multiplexed optical sensors to detect inflammatory cytokines in the tumor microenvironment.

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RWRyan M. WilliamsARAmelia K. RyanSRSyeda Rahman

Key Points

  • The aim is to develop a non-invasive method for monitoring inflammatory cytokine signaling in cancer.
  • Engineered multiplexed optical sensors for TNF-alpha, IL-6, and IL-12 using single-walled carbon nanotubes.
  • Non-covalent attachment of antibodies or ssDNA aptamers to sensors for specific detection.
  • Employed fluorescence changes to signal biomarker binding.
  • Quantitative performance with limits of detection in the clinical range.
  • Simultaneous detection of IL-6 and IL-12 in solution.
  • Ability to detect IL-6 excreted by stimulated macrophages.

Abstract

Abstract Inflammation is a hallmark of cancer development as well as a consequence of cancer progression. Chronic inflammatory pathways promote solid tumor growth, metastasis, and immune evasion. Indeed, chronic signaling of several inflammatory cytokines that lead to tumor formation include TNF-alpha, while persistent IL-6 signaling drives cell survival and proliferation as well as angiogenesis. IL-12, however, is a powerful anti-tumor cytokine, which promotes macrophage and T-cell cytotoxicity in addition to inhibiting angiogenesis. Despite their importance, it is difficult to model and monitor real-time inflammatory cytokine signaling in the tumor microenvironment during cancer initiation and progression. The ability to do so non-invasively in animal tumor models would allow for a better understanding of the key drivers of this important cancer hallmark, while the ability to do so in a patient could be a diagnostic and prognostic tool. To this end, we have engineered a multiplexed optical sensor platform for inflammatory cytokines TNF-alpha, IL-6, and IL-12. Individual sensors are synthesized from species-sorted single-walled carbon nanotubes (SWCNT), which exhibit tissue-transparent near-infrared fluorescence. For each cytokine, we non-covalently attached an antibody or ssDNA aptamer to SWCNT, allowing for molecularly-specific detection and a change in emission spectra upon biomarker binding. We found that sensor performance was quantitative with a limit of detection in the clinical range following inhibition of non-specific surface adsorption with passivation agent polymers and proteins. Further, we demonstrated the ability to detect IL-6 and IL-12, key pro-tumor and anti-tumor cytokines respectively, simultaneously in solution, as well as IL-6 excreted by macrophages in response to pro-inflammatory stimuli. Together, we anticipate further deployment of these inflammatory cytokine monitoring sensors in vivo and translation to patient diagnostic and prognostic profiling. Citation Format: Ryan M. Williams, Amelia Ryan, Syeda Rahman, Atara Israel. Engineered multiplexed optical sensors to detect inflammatory cytokines in the tumor microenvironment 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 726.

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Cite This Study

Williams et al. (2026) studied this question.

synapsesocial.com/papers/69d1fdd4a79560c99a0a4178https://doi.org/10.1158/1538-7445.am2026-726
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