Publication: Loss of Nm23 is associated with a more favorable
tumor microenvironment in patients with breast cancer
Authors
Durán, Esther ; Cárdenas, José Miguel ; Reina, Miguel Ángel ; Arriazu, Riánsares
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Publisher
F. Hernández y Juan F. Madrid. Universidad de Murcia: Departamento de Biología Celular e Histología
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DOI
https:/doi.org/10.14670/HH-30.345
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info:eu-repo/semantics/article
Description
Abstract
AIM: Nm23 is a metastasis suppressor gene
whose downregulation triggers metastatic progression.
The aim of this study was to investigate the expression
of Nm23 in breast carcinomas and its relationship with
tumor microenvironment markers. Methods: A
retrospective study was done (128 breast cancer patients
from 2007 to 2010). Nm23, LPA1, SMA, CD34, CD8,
and CD68 protein expressions were evaluated using
immunohistochemistry. Image analysis was used to
determine the immunostaining percentage area of Nm23,
LPA1, and SMA; the number of the total vessel fraction
CD34 positive; and the number of CD8+ and CD68+
cells. The mean ± SE was calculated. The differences
among groups were evaluated using Student t-test for
parametric data and Mann Whitney U test for
nonparametric data. Results: Cases were divided into
two groups: Nm23+ and Nm23-. LPA1 immunostaining
was significantly increased in Nm23- group.
Immunostaining percentage area of SMA was not
significantly higher when Nm23 was negative. CD34
immunopositive blood vessels, number of T CD8+ cells,
and the number of macrophage CD68+ cells were
increased when Nm23 was absent. Conclusion: Our
results suggest that the absence of Nm23 causes an
increase in LPA1, CD8+ and CD68+ inflammatory cells,
and angiogenesis marker. Therefore, Nm23 loss could be
associated with a more favorable environment for the
development and dissemination of breast cancer.
However, more studies are needed to determine this
association.
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Citation
Histology and Histopathology, Vol. 30, n.º 3 (2015)
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