CC BY 4.0 · TH Open 2017; 01(02): e155-e163
DOI: 10.1055/s-0037-1613674
Original Article
Georg Thieme Verlag KG Stuttgart · New York

Release of Prometastatic Platelet-Derived Microparticles Induced by Breast Cancer Cells: A Novel Positive Feedback Mechanism for Metastasis

Marta Zarà*
1   Department of Biology and Biotechnology, University of Pavia, Pavia, Italy
,
Gianni Francesco Guidetti*
1   Department of Biology and Biotechnology, University of Pavia, Pavia, Italy
,
Daniela Boselli
2   FRACTAL – San Raffaele Scientific Institute, Milan, Italy
,
Chiara Villa
2   FRACTAL – San Raffaele Scientific Institute, Milan, Italy
,
Ilaria Canobbio
1   Department of Biology and Biotechnology, University of Pavia, Pavia, Italy
,
Claudio Seppi
1   Department of Biology and Biotechnology, University of Pavia, Pavia, Italy
,
Caterina Visconte
1   Department of Biology and Biotechnology, University of Pavia, Pavia, Italy
,
Jessica Canino
1   Department of Biology and Biotechnology, University of Pavia, Pavia, Italy
,
Mauro Torti
1   Department of Biology and Biotechnology, University of Pavia, Pavia, Italy
› Author Affiliations
Further Information

Publication History

21 September 2017

08 November 2017

Publication Date:
15 December 2017 (online)

Abstract

Circulating platelets and platelet-derived microparticles are regulators of cancer metastasis. In this study, we show that breast cancer cells induce platelet aggregation and lead to the release of platelet-derived microparticles. Although able to cause comparable aggregation, the highly aggressive MDA-MB-231 cells were more potent than the poorly aggressive MCF7 cells in inducing platelet-derived microparticles release, which was comparable to that promoted by thrombin. MDA-MB-231 cells were able to bind and internalize both MCF7- and MDA-MB-231-induced platelet-derived microparticles with comparable efficiency. By contrast, MCF7 cells did not interact with either type of platelet-derived microparticles. Upon internalization, only platelet-derived microparticles released by platelet stimulation with MDA-MB-231 cells, but not those released upon stimulation with MCF7 cells, caused activation of MDA-MB-231 cells and promoted the phosphorylation of selected signaling proteins, including p38MAPK and myosin light chain. Accordingly, MDA-MB-231-induced, but not MCF7-induced, platelet-derived microparticles dose-dependently stimulated migration and invasion of targeted MDA-MB-231 cells. These results identify a novel paracrine positive feedback mechanism initiated by aggressive breast cancer cell types to potentiate their invasive phenotype through the release of platelet-derived microparticles.

* These authors contributed equally to this work.


 
  • References

  • 1 Mezouar S, Frère C, Darbousset R. , et al. Role of platelets in cancer and cancer-associated thrombosis: experimental and clinical evidences. Thromb Res 2016; 139: 65-76
  • 2 Erpenbeck L, Schön MP. Deadly allies: the fatal interplay between platelets and metastasizing cancer cells. Blood 2010; 115 (17) 3427-3436
  • 3 Gay LJ, Felding-Habermann B. Contribution of platelets to tumour metastasis. Nat Rev Cancer 2011; 11 (02) 123-134
  • 4 Yan M, Jurasz P. The role of platelets in the tumor microenvironment: From solid tumors to leukemia. Biochim Biophys Acta 2016; 1863 (03) 392-400
  • 5 Kopp HG, Placke T, Salih HR. Platelet-derived transforming growth factor-beta down-regulates NKG2D thereby inhibiting natural killer cell antitumor reactivity. Cancer Res 2009; 69 (19) 7775-7783
  • 6 Weber MR, Zuka M, Lorger M. , et al. Activated tumor cell integrin αvβ3 cooperates with platelets to promote extravasation and metastasis from the blood stream. Thromb Res 2016; 140 (Suppl. 01) S27-S36
  • 7 Vasina EM, Cauwenberghs S, Staudt M. , et al. Aging- and activation-induced platelet microparticles suppress apoptosis in monocytic cells and differentially signal to proinflammatory mediator release. Am J Blood Res 2013; 3 (02) 107-123
  • 8 Laffont B, Corduan A, Plé H. , et al. Activated platelets can deliver mRNA regulatory Ago2•microRNA complexes to endothelial cells via microparticles. Blood 2013; 122 (02) 253-261
  • 9 Mezouar S, Mege D, Darbousset R. , et al. Involvement of platelet-derived microparticles in tumor progression and thrombosis. Semin Oncol 2014; 41 (03) 346-358
  • 10 Laresche C, Pelletier F, Garnache-Ottou F. , et al. Increased levels of circulating microparticles are associated with increased procoagulant activity in patients with cutaneous malignant melanoma. J Invest Dermatol 2014; 134 (01) 176-182
  • 11 Tseng CC, Wang CC, Chang HC. , et al. Levels of circulating microparticles in lung cancer patients and possible prognostic value. Dis Markers 2013; 35 (05) 301-310
  • 12 Hron G, Kollars M, Weber H. , et al. Tissue factor-positive microparticles: cellular origin and association with coagulation activation in patients with colorectal cancer. Thromb Haemost 2007; 97 (01) 119-123
  • 13 Chaari M, Ayadi I, Rousseau A. , et al. Impact of breast cancer stage, time from diagnosis and chemotherapy on plasma and cellular biomarkers of hypercoagulability. BMC Cancer 2014; 14: 991
  • 14 Guidetti GF, Manganaro D, Consonni A, Canobbio I, Balduini C, Torti M. Phosphorylation of the guanine-nucleotide-exchange factor CalDAG-GEFI by protein kinase A regulates Ca(2+)-dependent activation of platelet Rap1b GTPase. Biochem J 2013; 453 (01) 115-123
  • 15 Canobbio I, Cipolla L, Guidetti GF. , et al. The focal adhesion kinase Pyk2 links Ca2+ signalling to Src family kinase activation and protein tyrosine phosphorylation in thrombin-stimulated platelets. Biochem J 2015; 469 (02) 199-210
  • 16 Heinmöller E, Weinel RJ, Heidtmann HH. , et al. Studies on tumor-cell-induced platelet aggregation in human lung cancer cell lines. J Cancer Res Clin Oncol 1996; 122 (12) 735-744
  • 17 Medina C, Jurasz P, Santos-Martinez MJ. , et al. Platelet aggregation-induced by caco-2 cells: regulation by matrix metalloproteinase-2 and adenosine diphosphate. J Pharmacol Exp Ther 2006; 317 (02) 739-745
  • 18 Janowska-Wieczorek A, Wysoczynski M, Kijowski J. , et al. Microvesicles derived from activated platelets induce metastasis and angiogenesis in lung cancer. Int J Cancer 2005; 113 (05) 752-760
  • 19 Janowska-Wieczorek A, Marquez-Curtis LA, Wysoczynski M, Ratajczak MZ. Enhancing effect of platelet-derived microvesicles on the invasive potential of breast cancer cells. Transfusion 2006; 46 (07) 1199-1209
  • 20 Chen M, Geng JG. P-selectin mediates adhesion of leukocytes, platelets, and cancer cells in inflammation, thrombosis, and cancer growth and metastasis. Arch Immunol Ther Exp (Warsz) 2006; 54 (02) 75-84
  • 21 Lonsdorf AS, Krämer BF, Fahrleitner M. , et al. Engagement of αIIbβ3 (GPIIb/IIIa) with ανβ3 integrin mediates interaction of melanoma cells with platelets: a connection to hematogenous metastasis. J Biol Chem 2012; 287 (03) 2168-2178
  • 22 Huang C, Jacobson K, Schaller MD. MAP kinases and cell migration. J Cell Sci 2004; 117 (Pt 20): 4619-4628
  • 23 Kim HK, Song KS, Park YS. , et al. Elevated levels of circulating platelet microparticles, VEGF, IL-6 and RANTES in patients with gastric cancer: possible role of a metastasis predictor. Eur J Cancer 2003; 39 (02) 184-191
  • 24 Li N. Platelets in cancer metastasis: to help the “villain” to do evil. Int J Cancer 2016; 138 (09) 2078-2087
  • 25 Dashevsky O, Varon D, Brill A. Platelet-derived microparticles promote invasiveness of prostate cancer cells via upregulation of MMP-2 production. Int J Cancer 2009; 124 (08) 1773-1777