Abstract 2190: Trib3 identified as a key therapeutic target for pancreatic cancer stem cells.

Abstract Background: Pancreatic ductal adenocarcinoma (PDAC) is among the most lethal cancers, exhibiting early dissemination and chemoresistance. These features are attributed to a specialized subpopulation of cancer stem cells (CSCs). Our lab has defined the cell of origin for PDAC within the pancreatic duct gland (PDG) stem cell compartment, a region crucial for epithelial renewal. Creation and maintenance of the CSC pool is hypothesized to underlie aggressive tumor biology, but transcriptional networks in this compartment remain poorly characterized. Objective: To define molecular pathways unique to pancreatic cancer stem cells (CSCs) that can be exploited as targeted therapies to eradicate CSCs while sparing normal pancreatic stem cells. Methods: Genetically engineered mouse models and single-cell RNA sequencing were used to trace and compare CSC-enriched (TTKS) and normal (TT) PDG organoids. Key findings were validated in other mouse and human PDAC models. Results: Single-cell analysis revealed broad upregulation of stem cell and CSC markers (Mthfd2, Slc7a5, Gadd45a), supporting conserved stem-like signatures in CSCs. Twelve genes were uniquely upregulated in PDAC CSCs, revealing new CSC-selective pathways. Trib3 was most strongly and widely upregulated among these, with multiple downstream regulators (β-catenin, FOXO1, ATF4) also enriched, indicating robust Trib3-driven network activation. Conclusion: Identification of a discrete PDG stem cell origin for PDAC enables detailed interrogation of CSC biology. Our model demonstrates that PDAC CSCs activate unique survival and adaptation pathways, with Trib3 emerging as a central regulator. Collectively, this provides new mechanistic insight and positions Trib3 as a compelling CSC-targeted therapeutic candidate.​​ Work is going on to understand the biological role of Trib3 in progression of CSCs in PDAC. Citation Format: Nirjhar M. Aloy, Kyle McAndrews, Adam Zulli, Kathryn Baldwin, Kristine Von Maltzan, Sarah Thayer. Trib3 identified as a key therapeutic target for pancreatic cancer stem cells [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 2190.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2190
Primary Topic
Cancer Cells and Metastasis
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article
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article

Abstract 2190: Trib3 identified as a key therapeutic target for pancreatic cancer stem cells.

Kyle L. McAndrews, Kristine von Maltzan, Nirjhar M. Aloy, Sarah P. Thayer et al.
Cancer Research
Cancer Cells and Metastasis
article

Abstract 2190: Trib3 identified as a key therapeutic target for pancreatic cancer stem cells.

Kyle L. McAndrews, Kristine von Maltzan, Nirjhar M. Aloy, Sarah P. Thayer, Adam Zulli, K. Baldwin
article en

Abstract

Abstract Background: Pancreatic ductal adenocarcinoma (PDAC) is among the most lethal cancers, exhibiting early dissemination and chemoresistance. These features are attributed to a specialized subpopulation of cancer stem cells (CSCs). Our lab has defined the cell of origin for PDAC within the pancreatic duct gland (PDG) stem cell compartment, a region crucial for epithelial renewal. Creation and maintenance of the CSC pool is hypothesized to underlie aggressive tumor biology, but transcriptional networks in this compartment remain poorly characterized. Objective: To define molecular pathways unique to pancreatic cancer stem cells (CSCs) that can be exploited as targeted therapies to eradicate CSCs while sparing normal pancreatic stem cells. Methods: Genetically engineered mouse models and single-cell RNA sequencing were used to trace and compare CSC-enriched (TTKS) and normal (TT) PDG organoids. Key findings were validated in other mouse and human PDAC models. Results: Single-cell analysis revealed broad upregulation of stem cell and CSC markers (Mthfd2, Slc7a5, Gadd45a), supporting conserved stem-like signatures in CSCs. Twelve genes were uniquely upregulated in PDAC CSCs, revealing new CSC-selective pathways. Trib3 was most strongly and widely upregulated among these, with multiple downstream regulators (β-catenin, FOXO1, ATF4) also enriched, indicating robust Trib3-driven network activation. Conclusion: Identification of a discrete PDG stem cell origin for PDAC enables detailed interrogation of CSC biology. Our model demonstrates that PDAC CSCs activate unique survival and adaptation pathways, with Trib3 emerging as a central regulator. Collectively, this provides new mechanistic insight and positions Trib3 as a compelling CSC-targeted therapeutic candidate.​​ Work is going on to understand the biological role of Trib3 in progression of CSCs in PDAC. Citation Format: Nirjhar M. Aloy, Kyle McAndrews, Adam Zulli, Kathryn Baldwin, Kristine Von Maltzan, Sarah Thayer. Trib3 identified as a key therapeutic target for pancreatic cancer stem cells [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 2190.

Cancer ResearchVol. 86(7_Supplement)
Nebraska Medical Center (US), University of Nebraska Medical Center (US), Louisiana State University Health Sciences Center Shreveport (US)
Openalex Percentile: Top 9%
Cancer Cells and Metastasis
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