The molecular interaction of ADAMTS-1 and fibulin-1 and its potential contribution to breast cancer biology

Yamina Mohamedi , Tania Fontanil , Teresa Cobo , José A. Vega , Juan L. Cobo , Olivia García-Suárez , Juan Cobo , Santiago Cal , Álvaro J. Obaya

Journal of Cancer Metastasis and Treatment ›› 2019, Vol. 5 : 37

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Journal of Cancer Metastasis and Treatment ›› 2019, Vol. 5:37 DOI: 10.20517/2394-4722.2018.81
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The molecular interaction of ADAMTS-1 and fibulin-1 and its potential contribution to breast cancer biology

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Abstract

Aim: Fibulins and ADAMTSs are two families of extracellular matrix proteins implicated in key functional and pathological processes. The fact that the fibulin-1 and ADAMTS-1 proteins interact raises new questions about the roles of these extracellular matrix proteins in modulating tumor progression. Herein, we described the functional implications of the interaction between fibulin-1 and ADAMTS-1 on the behavior of breast cancer cell lines.

Methods: Fibulin-1 and ADAMTS-1 were exogenously expressed in MCF-7 and MDA-MB-231 cell lines to assay the effect of their interaction in cellular properties.

Results: ADAMTS-1 expression exacerbates tumor effects in terms of proliferation, invasion and mammosphere formation. In contrast, the simultaneous expression of ADAMTS-1 and fibulin-1 impairs these effects. The analysis of the expression of both proteins in human breast cancer tissue arrays provides new insights into the complex roles of fibulin-1 and ADAMTS-1 in this type of tumor.

Conclusion: Our results suggests that the interaction between ADAMTS-1 and fibulin-1 induces a pronounced anti-tumoral effect.

Keywords

ADAMTS-1 / fibulin-1 / cell migration / cell proliferation / breast cancer / MCF-7 / MDA-MB-231

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Yamina Mohamedi, Tania Fontanil, Teresa Cobo, José A. Vega, Juan L. Cobo, Olivia García-Suárez, Juan Cobo, Santiago Cal, Álvaro J. Obaya. The molecular interaction of ADAMTS-1 and fibulin-1 and its potential contribution to breast cancer biology. Journal of Cancer Metastasis and Treatment, 2019, 5: 37 DOI:10.20517/2394-4722.2018.81

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