Oncotarget

Research Papers:

CIP4 promotes metastasis in triple-negative breast cancer and is associated with poor patient prognosis

Otto L.D. Cerqueira _, Peter Truesdell, Tomas Baldassarre, Santiago A. Vilella-Arias, Kathleen Watt, Jalna Meens, Harish Chander, Cynthia A.B. Osório, Fernando A. Soares, Eduardo M. Reis and Andrew W.B. Craig

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Oncotarget. 2015; 6:9397-9408. https://doi.org/10.18632/oncotarget.3351

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Abstract

Otto L.D. Cerqueira1, Peter Truesdell2, Tomas Baldassarre2, Santiago A. Vilella-Arias1, Kathleen Watt2, Jalna Meens2, Harish Chander2, Cynthia A.B. Osório3, Fernando A. Soares3,4, Eduardo M. Reis1,4, Andrew W.B. Craig2

1Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo, SP, Brazil

2Department of Biomedical and Molecular Sciences, Queen's University, and Division of Cancer Biology & Genetics, Queen's Cancer Research Institute, Kingston, ON, Canada

3Department of Anatomic Pathology, A.C. Camargo Hospital, São Paulo, SP, Brazil

4Instituto Nacional de Ciência e Tecnologia em Oncogenômica, São Paulo, SP, Brazil

Correspondence to:

Andrew W. Craig, e-mail: andrew.craig@queensu.ca

Eduardo M. Reis, e-mail: emreis@iq.usp.br

Keywords: metastasis, triple-negative breast cancer, CIP4

Received: October 22, 2014     Accepted: February 10, 2015     Published: March 19, 2015

ABSTRACT

Signaling via epidermal growth factor receptor (EGFR) and Src kinase pathways promote triple-negative breast cancer (TNBC) cell invasion and tumor metastasis. Here, we address the role of Cdc42-interacting protein-4 (CIP4) in TNBC metastasis in vivo, and profile CIP4 expression in human breast cancer patients. In human TNBC cells, CIP4 knock-down (KD) led to less sustained activation of Erk kinase and impaired cell motility compared to control cells. This correlated with significant defects in 3D invasion of surrounding extracellular matrix by CIP4 KD TNBC cells when grown as spheroid colonies. In mammary orthotopic xenograft assays using both human TNBC cells (MDA-MB-231, HCC 1806) and rat MTLn3 cells, CIP4 silencing had no overt effect on tumor growth, but significantly reduced the incidence of lung metastases in each tumor model. In human invasive breast cancers, high CIP4 levels was significantly associated with high tumor stage, TNBC and HER2 subtypes, and risk of progression to metastatic disease. Together, these results implicate CIP4 in promoting metastasis in TNBCs.


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