Abstract 7358: MYB expression increases progressively in pancreatic cancer, correlating with advancing tumor grade, metastasis, and poor patient survival

Abstract The transcription factor MYB plays a pivotal role in regulating cell proliferation, differentiation, and survival. Although it is amplified in a subset of pancreatic cancers, emerging evidence indicates that MYB overexpression may also arise through diverse regulatory mechanisms. We have previously demonstrated multiple oncogenic roles of MYB in pancreatic cancer pathogenesis; however, the temporal dynamics of its dysregulation during tumor progression remain poorly understood. Here, we investigated MYB expression across a spectrum of tissue samples representing normal, precancerous, and malignant stages of the pancreas, as well as matched liver metastases, by performing immunohistochemical analysis. The differential expression of MYB and its correlation with advancing tumor grade and patient survival were assessed using appropriate statistical analyses. We observed negligible expression of MYB in the normal pancreas, and its aberrant expression became noticeable in precancerous lesions, increasing progressively as the disease advanced. A high expression of MYB was also reported in metastatic lesions. Elevated MYB levels were positively correlated with higher tumor grade and significantly associated with reduced survival of pancreatic cancer patients. Interestingly, functional enrichment analyses of genes regulated by MYB overexpression suggested its involvement in key oncogenic programs, including proliferation, survival, epithelial-mesenchymal transition, and metastatic signaling pathways. These findings demonstrate that MYB dysregulation occurs early in pancreatic tumorigenesis and intensifies with disease progression, underscoring its potential as a biomarker for tumor aggressiveness and a potential target for therapeutic intervention. Citation Format: Shashi Anand, Kunwar Somesh Vikramdeo, Mohammad Aslam Khan, Lingling Xian, Paul M. Grandgenett, James Elliot Carter, Moh’d Khushman, Seema Singh, Ajay Pratap Singh. MYB expression increases progressively in pancreatic cancer, correlating with advancing tumor grade, metastasis, and poor patient survival [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 7358.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-7358
Primary Topic
FOXO transcription factor regulation
Type
article
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article

Abstract 7358: MYB expression increases progressively in pancreatic cancer, correlating with advancing tumor grade, metastasis, and poor patient survival

James Elliot Carter, Seema Singh, Kunwar Somesh Vikramdeo, Mohammad Aslam Khan et al.
Cancer Research
FOXO transcription factor regulation
article

Abstract 7358: MYB expression increases progressively in pancreatic cancer, correlating with advancing tumor grade, metastasis, and poor patient survival

James Elliot Carter, Seema Singh, Kunwar Somesh Vikramdeo, Mohammad Aslam Khan, Paul M. Grandgenett, Ajay Singh, Shashi Anand, Lingling Xian, Moh’d Khushman
article en

Abstract

Abstract The transcription factor MYB plays a pivotal role in regulating cell proliferation, differentiation, and survival. Although it is amplified in a subset of pancreatic cancers, emerging evidence indicates that MYB overexpression may also arise through diverse regulatory mechanisms. We have previously demonstrated multiple oncogenic roles of MYB in pancreatic cancer pathogenesis; however, the temporal dynamics of its dysregulation during tumor progression remain poorly understood. Here, we investigated MYB expression across a spectrum of tissue samples representing normal, precancerous, and malignant stages of the pancreas, as well as matched liver metastases, by performing immunohistochemical analysis. The differential expression of MYB and its correlation with advancing tumor grade and patient survival were assessed using appropriate statistical analyses. We observed negligible expression of MYB in the normal pancreas, and its aberrant expression became noticeable in precancerous lesions, increasing progressively as the disease advanced. A high expression of MYB was also reported in metastatic lesions. Elevated MYB levels were positively correlated with higher tumor grade and significantly associated with reduced survival of pancreatic cancer patients. Interestingly, functional enrichment analyses of genes regulated by MYB overexpression suggested its involvement in key oncogenic programs, including proliferation, survival, epithelial-mesenchymal transition, and metastatic signaling pathways. These findings demonstrate that MYB dysregulation occurs early in pancreatic tumorigenesis and intensifies with disease progression, underscoring its potential as a biomarker for tumor aggressiveness and a potential target for therapeutic intervention. Citation Format: Shashi Anand, Kunwar Somesh Vikramdeo, Mohammad Aslam Khan, Lingling Xian, Paul M. Grandgenett, James Elliot Carter, Moh’d Khushman, Seema Singh, Ajay Pratap Singh. MYB expression increases progressively in pancreatic cancer, correlating with advancing tumor grade, metastasis, and poor patient survival [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 7358.

Cancer ResearchVol. 86(7_Supplement)
Nebraska Medical Center (US), St. Jude Children's Research Hospital (US), Washington University in St. Louis (US), University of Mississippi Medical Center (US), University of Nebraska Medical Center (US), University of South Alabama (US)
No poverty
Openalex Percentile: Top 30%
FOXO transcription factor regulation
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