Oncotarget

Research Papers:

miR-155, identified as anti-metastatic by global miRNA profiling of a metastasis model, inhibits cancer cell extravasation and colonization in vivo and causes significant signaling alterations

Karina G. Thomsen _, Mikkel G. Terp, Rikke R. Lund, Rolf Søkilde, Daniel Elias, Martin Bak, Thomas Litman, Hans C. Beck, Maria B. Lyng and Henrik J. Ditzel

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Oncotarget. 2015; 6:29224-29239. https://doi.org/10.18632/oncotarget.4942

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Abstract

Karina G. Thomsen1,*, Mikkel G. Terp1,*, Rikke R. Lund1, Rolf Søkilde2, Daniel Elias1, Martin Bak3, Thomas Litman2, Hans C. Beck4, Maria B. Lyng1, Henrik J. Ditzel1,5

1Institute of Molecular Medicine, Department of Cancer and Inflammation Research, University of Southern Denmark, Odense, Denmark

2Department of Biomarker Discovery, Exiqon A/S, Vedbaek, Denmark

3Department of Pathology, Odense University Hospital, Odense, Denmark

4Centre for Clinical Proteomics, Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense, Denmark

5Department of Oncology, Odense University Hospital, Odense, Denmark

*These authors have contributed equally to this work

Correspondence to:

Henrik J. Ditzel, e-mail: hditzel@health.sdu.dk

Keywords: miR-155, cancer, colonization, LNA miRNA microarray, in vivo metastasis cell line model

Received: March 02, 2015     Accepted: July 29, 2015     Published: August 10, 2015

ABSTRACT

To gain insight into miRNA regulation in metastasis formation, we used a metastasis cell line model that allows investigation of extravasation and colonization of circulating cancer cells to lungs in mice. Using global miRNA profiling, 28 miRNAs were found to exhibit significantly altered expression between isogenic metastasizing and non-metastasizing cancer cells, with miR-155 being the most differentially expressed. Highly metastatic mesenchymal-like CL16 cancer cells showed very low miR-155 expression, and miR-155 overexpression in these cells lead to significantly decreased tumor burden in lungs when injected intravenously in immunodeficient mice. Our experiments addressing the underlying mechanism of the altered tumor burden revealed that miR-155-overexpressing CL16 cells were less invasive than CL16 control cells in vitro, while miR-155 overexpression had no effect on cancer cell proliferation or apoptosis in established lung tumors. To identify proteins regulated by miR-155 and thus delineate its function in our cell model, we compared the proteome of xenograft tumors derived from miR-155-overexpressing CL16 cells and CL16 control cells using mass spectrometry-based proteomics. >4,000 proteins were identified, of which 92 were consistently differentially expressed. Network analysis revealed that the altered proteins were associated with cellular functions such as movement, growth and survival as well as cell-to-cell signaling and interaction. Downregulation of the three metastasis-associated proteins ALDH1A1, PIR and PDCD4 in miR-155-overexpressing tumors was validated by immunohistochemistry. Our results demonstrate that miR-155 inhibits the ability of cancer cells to extravasate and/or colonize at distant organs and brings additional insight into the complexity of miR-155 regulation in metastatic seeding.


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