Angiotensin II Facilitates Breast Cancer Cell Migration and Metastasis


Autoria(s): Rodrigues-Ferreira, Sylvie; Abdelkarim, Mohamed; Dillenburg-Pilla, Patricia; Luissint, Anny-Claude; di-Tommaso, Anne; Deshayes, Frederique; Pontes, Carmen Lucia S.; Molina, Angie; Cagnard, Nicolas; Letourneur, Franck; Morel, Marina; Reis, Rosana I.; Casarini, Dulce E.; Terris, Benoit; Couraud, Pierre-Olivier; Costa Neto, Claudio Miguel da; Di Benedetto, Melanie; Nahmias, Clara
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

29/10/2013

29/10/2013

02/08/2013

Resumo

Breast cancer metastasis is a leading cause of death by malignancy in women worldwide. Efforts are being made to further characterize the rate-limiting steps of cancer metastasis, i.e. extravasation of circulating tumor cells and colonization of secondary organs. In this study, we investigated whether angiotensin II, a major vasoactive peptide both produced locally and released in the bloodstream, may trigger activating signals that contribute to cancer cell extravasation and metastasis. We used an experimental in vivo model of cancer metastasis in which bioluminescent breast tumor cells (D3H2LN) were injected intra-cardiacally into nude mice in order to recapitulate the late and essential steps of metastatic dissemination. Real-time intravital imaging studies revealed that angiotensin II accelerates the formation of metastatic foci at secondary sites. Pre-treatment of cancer cells with the peptide increases the number of mice with metastases, as well as the number and size of metastases per mouse. In vitro, angiotensin II contributes to each sequential step of cancer metastasis by promoting cancer cell adhesion to endothelial cells, trans-endothelial migration and tumor cell migration across extracellular matrix. At the molecular level, a total of 102 genes differentially expressed following angiotensin II pretreatment were identified by comparative DNA microarray. Angiotensin II regulates two groups of connected genes related to its precursor angiotensinogen. Among those, up-regulated MMP2/MMP9 and ICAM1 stand at the crossroad of a network of genes involved in cell adhesion, migration and invasion. Our data suggest that targeting angiotensin II production or action may represent a valuable therapeutic option to prevent metastatic progression of invasive breast tumors.

University Paris Descartes

University Paris Descartes

Inserm

INSERM

Centre National de la Recherche Scientifique

Centre National de la Recherche Scientifique

Ligue Contre le Cancer-Comite Ile de France

Ligue Contre le CancerComite Ile de France

Association pour la Recherche contre le Cancer (ARC)

Association pour la Recherche contre le Cancer (ARC)

Fondation RAJA

Fondation RAJA

association Prolific

association Prolific

Identificador

PLOS ONE, SAN FRANCISCO, v. 7, n. 4, supl. 1, Part 2, pp. 80-82, APR 20, 2012

1932-6203

http://www.producao.usp.br/handle/BDPI/36400

10.1371/journal.pone.0035667

http://dx.doi.org/10.1371/journal.pone.0035667

Idioma(s)

eng

Publicador

PUBLIC LIBRARY SCIENCE

SAN FRANCISCO

Relação

PLOS ONE

Direitos

openAccess

Copyright PUBLIC LIBRARY SCIENCE

Palavras-Chave #HUMAN GASTRIC-CANCER #TYPE-1 RECEPTOR #TUMOR ANGIOGENESIS #GROWTH #MICROENVIRONMENT #SYSTEM #RISK #DISSEMINATION #METAANALYSIS #PROGRESSION #MULTIDISCIPLINARY SCIENCES
Tipo

article

original article

publishedVersion