Abstract 3965: Spatialomics detection of neuroendocrine involvement in cancer tissue

Abstract The study of neuroendocrine involvement observed in inflammation, neuronal damage, cancer, and neurodegenerative disease is an emerging field offering new opportunities of intervention and treatment of currently intractable disease. Cancer cells are known to invade the space surrounding neurons (perineuronal invasion) and derive pro-survival and anti-apoptotic benefits from the nerve fibers and their neurotransmitters, secreted amines and peptides. Formation of new neural tissue is a characteristic of cancer with poor prognosis. We present a spatial-omics approach of multiplexing immunohistochemistry (IHC) with mRNA in situ hybridization (ISH) detection to examine the microenvironment of neuroendocrine involvement and the biomarkers relevant to these tissues and infiltrating immune cells. We image both protein and mRNA abundance and distribution in FFPE tissue with neuroendocrine involvement. ISH detection uses single stranded branched DNA amplification scheme (ss-bDNA) for single molecule detection, while IHC detection uses direct antibody labeling for moderate and high abundant targets and enzymatic signal amplification for low abundant targets. We present protocol modifications with significant improvements minimizing incompatibility between IHC and ISH otherwise resulting in diminished or loss of signal. These modifications retain IHC and ISH signal, minimize auto-fluorescence, and shorten protocol time required for multiplexed workflows. We show multiplex IHC labeling of neural biomarkers such as S100B, CD56, glial fibrillary acidic protein (GFAP), chromogranin A (CgA) and synaptophysin in relevant tissue which are often over-expressed in non-endocrine structures and tissues of some tumors, and in neurodegenerative disease models. The presence of neural mRNA expression, combined with immune markers such as FoxP3 and PD-1, PD-L1 and proliferation markers of PCNA and Ki-67 in cancer tissue, reveal the neuroendocrine involvement in the tumor immune microenvironment. For Research Use Only. Not for use in diagnostic procedures. Citation Format: Scott T. Clarke, Chris Vonnegut, Leticia Montoya, Mae Voeun, Wenjun Zhou, Anna Cartier, Aleksey Rukavishnikov. Spatialomics detection of neuroendocrine involvement in cancer tissue [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 3965.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-3965
Primary Topic
Cancer Research and Treatments
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article
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article

Abstract 3965: Spatialomics detection of neuroendocrine involvement in cancer tissue

Chris L. Vonnegut, Leticia Montoya, Anna Cartier, Mae Voeun et al.
Cancer Research
Cancer Research and Treatments
article

Abstract 3965: Spatialomics detection of neuroendocrine involvement in cancer tissue

Chris L. Vonnegut, Leticia Montoya, Anna Cartier, Mae Voeun, Scott T. Clarke, Wenjun Zhou, Aleksey Rukavishnikov
article en

Abstract

Abstract The study of neuroendocrine involvement observed in inflammation, neuronal damage, cancer, and neurodegenerative disease is an emerging field offering new opportunities of intervention and treatment of currently intractable disease. Cancer cells are known to invade the space surrounding neurons (perineuronal invasion) and derive pro-survival and anti-apoptotic benefits from the nerve fibers and their neurotransmitters, secreted amines and peptides. Formation of new neural tissue is a characteristic of cancer with poor prognosis. We present a spatial-omics approach of multiplexing immunohistochemistry (IHC) with mRNA in situ hybridization (ISH) detection to examine the microenvironment of neuroendocrine involvement and the biomarkers relevant to these tissues and infiltrating immune cells. We image both protein and mRNA abundance and distribution in FFPE tissue with neuroendocrine involvement. ISH detection uses single stranded branched DNA amplification scheme (ss-bDNA) for single molecule detection, while IHC detection uses direct antibody labeling for moderate and high abundant targets and enzymatic signal amplification for low abundant targets. We present protocol modifications with significant improvements minimizing incompatibility between IHC and ISH otherwise resulting in diminished or loss of signal. These modifications retain IHC and ISH signal, minimize auto-fluorescence, and shorten protocol time required for multiplexed workflows. We show multiplex IHC labeling of neural biomarkers such as S100B, CD56, glial fibrillary acidic protein (GFAP), chromogranin A (CgA) and synaptophysin in relevant tissue which are often over-expressed in non-endocrine structures and tissues of some tumors, and in neurodegenerative disease models. The presence of neural mRNA expression, combined with immune markers such as FoxP3 and PD-1, PD-L1 and proliferation markers of PCNA and Ki-67 in cancer tissue, reveal the neuroendocrine involvement in the tumor immune microenvironment. For Research Use Only. Not for use in diagnostic procedures. Citation Format: Scott T. Clarke, Chris Vonnegut, Leticia Montoya, Mae Voeun, Wenjun Zhou, Anna Cartier, Aleksey Rukavishnikov. Spatialomics detection of neuroendocrine involvement in cancer tissue [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 3965.

Cancer ResearchVol. 86(7_Supplement)
Thermo Fisher Scientific (United States) (US)
Good health and well-being
Openalex Percentile: Top 8%
Cancer Research and Treatments
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