Large cell carcinoma (LCC) is a rare and aggressive lung cancer subtype with poor prognosis and no targeted therapies. Tumor-associated fibroblasts (TAFs) derived from LCC tumors exhibit premature senescence, and coculture of pulmonary fibroblasts with LCC cell lines selectively induces fibroblast senescence, which in turn drives LCC cell growth and invasion. Here we identify MMP1 as overexpressed specifically in LCC cell lines, and we show that expression of MMP1 by LCC cells is necessary for induction of fibroblast senescence and consequent tumor promotion in both cell culture and mouse models. We also show that MMP1, in combination with TGF-β1, is sufficient to induce fibroblast senescence and consequent LCC promotion. Furthermore, we implicate PAR-1 and oxidative stress in MMP1/TGF-β1-induced TAF senescence. Our results establish an entirely new role for MMP1 in cancer, and support a novel therapeutic strategy in LCC based on targeting senescent TAFs.

MMP1 drives tumor progression in large cell carcinoma of the lung through fibroblast senescence / M. Gabasa, E.S. Radisky, R. Ikemori, G. Bertolini, M. Arshakyan, A. Hockla, P. Duch, O. Rondinone, A. Llorente, M. Maqueda, A. Davalos, E. Gavilan, A. Perera, J. Ramirez, P. Gascon, N. Reguart, L. Roz, D.C. Radisky, J. Alcaraz. - In: CANCER LETTERS. - ISSN 0304-3835. - 507:(2021 Jun), pp. 1-12. [10.1016/j.canlet.2021.01.028]

MMP1 drives tumor progression in large cell carcinoma of the lung through fibroblast senescence

O. Rondinone;
2021

Abstract

Large cell carcinoma (LCC) is a rare and aggressive lung cancer subtype with poor prognosis and no targeted therapies. Tumor-associated fibroblasts (TAFs) derived from LCC tumors exhibit premature senescence, and coculture of pulmonary fibroblasts with LCC cell lines selectively induces fibroblast senescence, which in turn drives LCC cell growth and invasion. Here we identify MMP1 as overexpressed specifically in LCC cell lines, and we show that expression of MMP1 by LCC cells is necessary for induction of fibroblast senescence and consequent tumor promotion in both cell culture and mouse models. We also show that MMP1, in combination with TGF-β1, is sufficient to induce fibroblast senescence and consequent LCC promotion. Furthermore, we implicate PAR-1 and oxidative stress in MMP1/TGF-β1-induced TAF senescence. Our results establish an entirely new role for MMP1 in cancer, and support a novel therapeutic strategy in LCC based on targeting senescent TAFs.
Cancer-associated fibroblasts; lung cancer; MMP1; senescence; TGF-β; Animals; Cancer-Associated Fibroblasts; Carcinoma, Large Cell; Cell Line, Tumor; Coculture Techniques; Disease Progression; Female; Gene Expression Regulation, Neoplastic; Humans; Lung Neoplasms; Matrix Metalloproteinase 1; Mice, Nude; Oxidative Stress; Paracrine Communication; Receptor, PAR-1; Signal Transduction; Transforming Growth Factor beta1; Tumor Burden; Cell Proliferation; Cellular Senescence
Settore MED/06 - Oncologia Medica
giu-2021
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/912923
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