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Elevated tissue expression of RANKL and RANK is associated with poorer survival rates in pancreatic cancer patients.

Authors :
Ortega MA
Jiménez-Álvarez L
Fraile-Martinez O
Garcia-Montero C
De León-Oliva D
Toledo-Lobo MDV
Palacios E
Granado P
Esteban A
Guijarro LG
Pekarek L
Asúnsolo Á
López-González L
Bujan J
García-Honduvilla N
Álvarez-Mon M
Saez MA
Díaz-Pedrero R
Source :
Histology and histopathology [Histol Histopathol] 2024 Sep; Vol. 39 (9), pp. 1133-1140. Date of Electronic Publication: 2023 Dec 29.
Publication Year :
2024

Abstract

Pancreatic cancer is a highly lethal malignancy with a growing incidence reported worldwide. Pancreatic ductal adenocarcinoma (PDAC) is the most common type of pancreatic cancer, which is often diagnosed at advanced stages, making its prognosis and medical management difficult. The identification of histopathological biomarkers has allowed a more precise stratification of pancreatic cancer patients, providing additional information about their prognosis and offering possible therapeutic targets to be explored. The prognostic value of the receptor activator of nuclear factor-kappa B (RANK) and its ligand (RANKL) has been evaluated in breast and prostate tumors, however, their usefulness has not been assessed in pancreatic cancer. In the present work, we analyzed the relationship between the protein expression of RANK and RANKL with the survival of 41 patients with pancreatic cancer followed for 60 months, by performing immunohistochemistry and Kaplan-Meier curves. Our results demonstrate a direct association of high expression levels of RANK and RANKL with poorer survival of pancreatic cancer patients in comparison to those with low/medium and null expression levels of both markers. Further studies should be conducted to explore the carcinogenic role of both components in this type of tumor, as well as additional promising translational uses.<br /> (©The Author(s) 2023. Open Access. This article is licensed under a Creative Commons CC-BY International License.)

Details

Language :
English
ISSN :
1699-5848
Volume :
39
Issue :
9
Database :
MEDLINE
Journal :
Histology and histopathology
Publication Type :
Academic Journal
Accession number :
38230588
Full Text :
https://doi.org/10.14670/HH-18-700