Published December 3, 2010 | Version v1
Journal article

Study of TLR3, TLR4 and TLR9 in breast carcinomas and their association with metastasis

  • 1. Unidad de Investigación, Fundación Hospital de Jove, Gijón (Spain)
  • 2. Servicio de Anatomía Patológica, Fundación Hospital de Jove, Gijón (Spain)
  • 3. Servicio de Cirugía General, Fundación Hospital de Jove, Gijón (Spain)

Description

Toll-like receptors (TLRs) have garnered an extraordinary amount of interest in cancer research due to their role in tumor progression. By activating the production of several biological factors, TLRs induce type I interferons and other cytokines, which drive an inflammatory response and activate the adaptive immune system. The aim of this study was to investigate the expression and clinical relevance of TLR3, 4 and 9 in breast cancer. The expression levels of TLR3, TLR4 and TLR9 were analyzed on tumors from 74 patients with breast cancer. The analysis was performed by immunohistochemistry. Samples of carcinomas with recurrence exhibited a significant increase in the mRNA levels of TLR3, TLR4 and TLR9. Tumors showed high expression of TLRs expression levels by cancer cells, especially TLR4 and 9. Nevertheless, a significant percentage of tumors also showed TLR4 expression by mononuclear inflammatory cells (21.6%) and TLR9 expression by fibroblast-like cells (57.5%). Tumors with high TLR3 expression by tumor cell or with high TLR4 expression by mononuclear inflammatory cells were significantly associated with higher probability of metastasis. However, tumours with high TLR9 expression by fibroblast-like cells were associated with low probability of metastasis. The expression levels of TLR3, TLR4 and TLR9 have clinical interest as indicators of tumor aggressiveness in breast cancer. TLRs may represent therapeutic targets in breast cancer

Availability note (English)

Available from http://dx.doi.org/10.1186/1471-2407-10-665; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009680

Additional details

Publishing Information

Journal Title
BMC cancer (Online)
Journal Volume
10
Journal Page Range
p. 665
ISSN
1471-2407

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
46098778
Subject category
S60: APPLIED LIFE SCIENCES; S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
CARCINOMAS; FIBROBLASTS; INTERFERON; MAMMARY GLANDS; PATIENTS; RECEPTORS; TUMOR CELLS
Descriptors DEC
ANIMAL CELLS; BODY; CONNECTIVE TISSUE CELLS; DISEASES; GLANDS; GROWTH FACTORS; LYMPHOKINES; MEMBRANE PROTEINS; MITOGENS; NEOPLASMS; ORGANIC COMPOUNDS; ORGANS; PROTEINS; SOMATIC CELLS

Optional Information

Copyright
Copyright (c)2010 Gonz#Latin Small Letter A With Acute#lez-Reyes et al
Notes
PMCID: PMC3009680; PUBLISHER-ID: 1471-2407-10-665; PMID: 21129170; OAI: oai:pubmedcentral.nih.gov:3009680; licensee BioMed Central Ltd.