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Force-feeding malignant mesothelioma stem-cell like with exosome-delivered miR-126 induces tumour cell killing
Institution:1. Department of Clinical and Molecular Sciences, Polytechnic University of Marche, Ancona, Italy;2. RNA biology Group, International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy;3. Cardiovascular Biology Laboratory, International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy;4. Institute for Maternal and Child Health - IRCCS \"Burlo Garofolo\", Trieste, Italy;5. Department of Excellence SBSP-Biomedical Sciences and Public Health, Polytechnic University of Marche, Ancona, Italy;6. Department of Medical Sciences, Clinical Unit of Occupational Medicine, University of Trieste, Trieste, Italy
Abstract:Malignant pleural mesothelioma (MPM) is an aggressive tumour resistant to treatments. It has been postulated that cancer stem cells (CSCs) persist in tumours causing relapse after multimodality treatment. In the present study, a novel miRNA-based therapy approach is proposed. MPM-derived spheroids have been treated with exosome-delivered miR-126 (exo-miR) and evaluated for their anticancer effect. The exo-miR treatment increased MPM stem-cell like stemness and inhibited cell proliferation. However, at a prolonged time, the up taken miR-126 was released by the cells themselves through exosomes; the inhibition of exosome release by an exosome release inhibitor GW4869 induced miR-126 intracellular accumulation leading to massive cell death and in vivo tumour growth arrest. Autophagy is involved in these processes; miR-126 accumulation induced a protective autophagy and the inhibition of this process by GW4869 generates a metabolic crisis that promotes necroptosis, which was associated with PARP-1 over-expression and cyt-c and AIF release. Here, for the first time, we proposed a therapy against CSCs, a heterogeneous cell population involved in cancer development and relapse.
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