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Updated: Mar 28, 2026

Oncogene Expression Analysis with Alterations in pH in a Pancreatic Ductal Cell Line
Published on: April 11, 2025
Microarray-based gene expression profiling reveals genes and pathways involved in the oncogenic function of REG3A on
Qianqian Xu1, Rong Fu1, Guoxiao Yin1
1Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Abstract:
We previously reported that regenerating islet-derived protein 3 alpha (REG3A) exacerbates pancreatic malignancies. The mechanism of this effect has not been clearly elucidated. Here we first identified key differentially expressed genes (DEGs) and signal pathways in the pancreatic cancer cell line SW1990, compared to two control cell lines, by microarray analysis. We then identified key genes and pathways regulated by REG3A or the cytokine IL6 in SW1990 cells. Afterwards, these DEGs induced by REG3A or IL6 were subjected to KEGG pathway enrichment analysis and GO function analysis by the DAVID online tool. Ultimately, we constructed protein-protein interaction networks among the DEGs by Cytoscape. Among the three pancreatic cell lines, SW1990 exhibited highly deterioration with the activation of genes and pathways related to proliferation, survival, angiogenesis, and invasion. As a result, 50 DEGs enriched in 11 pathways were identified in REG3A-treated SW1990 cells, and 28 DEGs enriched in 9 pathways were detected in IL6-treated cells. Overall, results of microarray analysis followed by qRT-PCR and Western blotting suggest that REG3A regulates pancreatic cell growth by increasing the expression of at least 8 genes: JAK1, STAT3, IL10, FOXM1, KRAS, MYC, CyclinD1, and c-fos; and activation of at least 4 signal pathways: TGFβ, PDGF, angiogenesis and RAS. Similar results were obtained with IL6 treatment. Regulation network analysis confirmed the cell growth related DEGs, and further uncovered three transcription factor families with immune functions regulated by REG3A.
Insights
Regenerating islet-derived protein 3 alpha (REG3A) promotes pancreatic cancer growth by activating key genes and pathways like JAK1, STAT3, and TGFβ. This protein also influences immune functions, highlighting its role in pancreatic malignancies.
Area of Science:
- Oncology
- Molecular Biology
- Genomics
Background:
- Pancreatic cancer is a deadly malignancy with complex molecular underpinnings.
- Regenerating islet-derived protein 3 alpha (REG3A) has been implicated in exacerbating pancreatic cancer.
- The precise mechanisms by which REG3A influences pancreatic cancer progression remain unclear.
Purpose of the Study:
- To elucidate the molecular mechanisms by which REG3A promotes pancreatic cancer progression.
- To identify key genes and signaling pathways regulated by REG3A in pancreatic cancer cells.
- To explore the regulatory network of REG3A in pancreatic cancer.
Main Methods:
- Microarray analysis was used to identify differentially expressed genes (DEGs) in SW1990 pancreatic cancer cells.
- Quantitative real-time PCR (qRT-PCR) and Western blotting were employed for validation.
- KEGG pathway enrichment, GO function analysis, and protein-protein interaction network construction (using Cytoscape) were performed.
Main Results:
- REG3A treatment in SW1990 cells led to the identification of 50 DEGs enriched in 11 pathways, including those related to proliferation, survival, angiogenesis, and invasion.
- REG3A upregulates key genes such as JAK1, STAT3, IL10, FOXM1, KRAS, MYC, CyclinD1, and c-fos.
- Activation of signaling pathways including TGFβ, PDGF, angiogenesis, and RAS was observed, similar to IL6 treatment.
Conclusions:
- REG3A significantly contributes to pancreatic cancer cell growth and progression.
- REG3A regulates pancreatic cancer via a network of genes including JAK1, STAT3, and KRAS, and pathways like TGFβ and angiogenesis.
- REG3A also influences transcription factors with immune functions, suggesting a broader role in the tumor microenvironment.
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