Toll-like receptor 3: implications for proinflammatory microenvironment in human breast cancer


Autoria(s): Amarante, Marla Karine; Oliveira, Karen Brajao de; Guembarovski, Roberta Losi; Herrera, Ana Cristina da Silva do Amaral; Guembarovski, Alda Losi; Jorge Sobrinho, Walter; Voltarelli, Julio Cesar; Watanabe, Maria Angelica Ehara
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

06/11/2013

06/11/2013

2012

Resumo

Under many circumstances, the host constituents that are found in the tumor microenvironment support a malignancy network and provide the cancer cells with advantages in proliferation, invasiveness and metastasis establishment at remote organs. It is known that Toll like receptors (TLRs) are expressed not only on immune cells but also on cancer cells and it has suggested a deleterious role for TLR3 in inflammatory disease. Hypothesizing that altered IFN gamma signaling may be a key mechanism of immune dysfunction common to cancer as well CXCR4 is overexpressed among breast cancer patients, the mRNA expression of TLR3, CXCR4 and IFN gamma in breast cancer tumor tissues was investigated. No statistically significant differences in the expression of CXCR4 mRNA, IFN gamma and TLR3 between healthy and tumor tissues was observed, however, it was verified a positive correlation between mRNA relative expression of TLR3 and CXCR4 (p < 0.001), and mRNA relative expression of TLR3 was significantly increased in breast cancer tumor tissue when compared to healthy mammary gland tissue among patients expressing high IFN gamma (p = 0.001). Since the tumor microenvironment plays important roles in cancer initiation, growth, progression, invasion and metastasis, it is possible to propose that an overexpression of IFN gamma mRNA due to the pro-inflammatory microenvironment can lead to an up-regulation of CXCR4 mRNA and consequently to an increased TLR3 mRNA expression even among nodal negative patients. In the future, a comprehensive study of TLR3, CXCR4 and IFN gamma axis in primary breast tumors and corresponding healthy tissues will be crucial to further understanding of the cancer network.

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Fundacao Araucaria (PPSUS)

Londrina State University Graduate Administration (PROPPGUEL)

Identificador

MOLECULAR BIOLOGY REPORTS, DORDRECHT, v. 39, n. 12, pp. 11087-11092, DEC, 2012

0301-4851

http://www.producao.usp.br/handle/BDPI/42430

10.1007/s11033-012-2013-1

http://dx.doi.org/10.1007/s11033-012-2013-1

Idioma(s)

eng

Publicador

SPRINGER

DORDRECHT

Relação

MOLECULAR BIOLOGY REPORTS

Direitos

closedAccess

Copyright SPRINGER

Palavras-Chave #TLR3 #IFN GAMMA #CXCR4 #BREAST CANCER #DOUBLE-STRANDED-RNA #INNATE IMMUNITY #BLOOD-CELLS #TLR3 #ACTIVATION #EXPRESSION #CXCR4 #BIOCHEMISTRY & MOLECULAR BIOLOGY
Tipo

article

original article

publishedVersion