Publication: The prognostic impact of
tumor-associated macrophages and intra-tumoral
apoptosis in non-small cell lung cancer
Authors
Becker, Matheus ; Müller, Carolina Beatriz ; De Bastiani, Marco Antônio ; Klamt, Fábio
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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
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info:eu-repo/semantics/article
Description
Abstract
Summary. Lung cancer is the leading cause of cancerrelated
deaths worldwide. Non-small cell lung cancer
(NSCLC) accounts for 80% of all lung malignancies.
Tumor-associated macrophages (TAM) are abundant
components of NSCLC. Although under certain
conditions TAM can kill tumor cells, they can also act as
tumor promoters secreting a variety of factors that
directly stimulate tumor invasion and metastasis. TAM
presents two distinct phenotypes: the classically
activated (or M1) phenotype, which is highly proinflammatory
(phagocytic and cytotoxic), and the
alternatively activated (or M2) phenotype, which has
anti-inflammatory and pro-tumoral properties. The
polarization status of TAM depends on stimulating
factors from the tumor microenvironment, and some in
vitro evidence implies that the phagocytosis of apoptotic
bodies derived from tumoral cells is a key factor in
M1/M2 modulation, raising the question of whether the
evaluation of the apoptotic index (AI) and macrophage
polarization have a prognostic role in NSCLC patient
survival. The present article systematically reviewed the
published series of clinical data that correlated the AI
and/or macrophage densities and polarization status
(M1/M2) with the outcome of non-small cell lung cancer
patients. Even though an overwhelming body of clinical
data support that TAM’s density, micro-anatomical
localization, phenotype and intra-tumoral AI are
independent predictors of survival time, no study to date
has been conducted to evaluate the impact of these
parameters altogether in NSCLC patient outcome. Joint
analysis of these biologic factors in future studies might
reveal their prognostic value in the management of
NSCLC cases.
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Citation
Histol Histopathol, vol. 29, nº 1, (2014)
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