Expression of p53 and C-Myc in pancreatic ductal adenocarcinoma and their association with clinicopathological, molecular, prognostic and survival variables in patients of Fundación Santa Fe de Bogotá University Hospital, between 2009-2022.

dc.contributor.authorJohanna Álvarez
dc.contributor.authorGabriela Rozo-Paz
dc.contributor.authorDaniela Castellanos-Leguizamón
dc.contributor.authorJavier Baena-Del Valle
dc.contributor.authorAlonso Vera-Torres
dc.contributor.authorViviana Barrera-Penagos
dc.contributor.authorDaniel González‐Moreno
dc.contributor.authorDiana Marcela Grajales-Urrego
dc.contributor.authorRocío López
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T20:51:04Z
dc.date.available2026-03-22T20:51:04Z
dc.date.issued2025
dc.description.abstractBackground. Pancreatic ductal adenocarcinoma (PDAC) has a high mortality rate despite treatment. This study compares the expression of C-Myc and p53 with clinicopathological, molecular, and prognostic factors in PDAC patients at the Fundación Santa Fe University Hospital in Bogotá. Methodology. This descriptive-analytical study included 95 PDAC patients, 55 of whom underwent surgical resection and 40 were only biopsied. Clinicopathological data was obtained from histological analyses and medical records. Expression of C-Myc and p53 was determined by immunohistochemistry. Statistical analysis was done using R-studio version 2023.12.1. Results. The study group consisted of 52 women (54.7%) and 43 men (45.3%), aged 41-89 years (M = 66.8). No significant associations were found between molecular marker expression and clinicopathological variables. However, patients with PDAC in the pancreas body or liver metastases had a higher likelihood of surviving less than 3 years. Among surgical patients (N = 54), 38 expressed C-Myc and 39 expressed p53. Aberrant p53 expression was linked to decreased disease-free survival in patients with a <3-year survival post diagnosis (t[23] = -2.42; p < .05). Similarly, higher C-Myc expression was seen in patients with postsurgical recurrence with a <3-year survival post diagnosis (t[21] = -2.28; p < .05). Conclusion. Targeted therapies for these genes may improve PDAC prognosis. Further research should investigate other biomarkers and their expression in neoplastic and preserved pancreatic tissue.
dc.identifier.doi10.22541/au.174664998.87015473/v1
dc.identifier.urihttps://doi.org/10.22541/au.174664998.87015473/v1
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/84442
dc.language.isoen
dc.sourceFundación Santa Fe de Bogotá
dc.subjectPancreatic ductal adenocarcinoma
dc.subjectInternal medicine
dc.subjectOncology
dc.subjectMedicine
dc.subjectAssociation (psychology)
dc.subjectExpression (computer science)
dc.subjectCancer research
dc.titleExpression of p53 and C-Myc in pancreatic ductal adenocarcinoma and their association with clinicopathological, molecular, prognostic and survival variables in patients of Fundación Santa Fe de Bogotá University Hospital, between 2009-2022.
dc.typepreprint

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