Thyroid carcinoma is generally associated with good prognosis, but no effective treatments are currently available for aggressive forms not cured by standard therapy. To find novel therapeutic targets for this tumor type, we had previously performed a siRNA-based functional screening to identify genes essential for sustaining the oncogenic phenotype of thyroid tumor cells, but not required to the same extent for the viability of normal cells (non-oncogene addiction paradigm). Among those, we found the coatomer protein complex ζ1 (COPZ1) gene, which is involved in intracellular traffic, autophagy and lipid homeostasis. In this paper, we investigated the mechanisms through which COPZ1 depletion leads to thyroid tumor cell death. We showed that siRNA-mediated COPZ1 depletion causes abortive autophagy, endoplasmic reticulum stress, unfolded protein response and apoptosis. Interestingly, we observed that mouse tumor xenografts, locally treated with siRNA targeting COPZ1, showed a significant reduction of tumor growth. On the whole, we demonstrated for the first time the crucial role of COPZ1 in the viability of thyroid tumor cells, suggesting that it may be considered an attractive target for novel therapeutic approaches for thyroid cancer.
Targeting COPZ1 non-oncogene addiction counteracts the viability of thyroid tumor cells / M..C. Anania, E. Cetti, D. Lecis, K. Todoerti, A. Gulino, G. Mauro, T. Di Marco, L. Cleris, S. Pagliardini, G. Manenti, B. Belmonte, C. Tripodo, A. Neri, A. Greco. - In: CANCER LETTERS. - ISSN 0304-3835. - 410(2017 Dec 01), pp. 201-211.
|Titolo:||Targeting COPZ1 non-oncogene addiction counteracts the viability of thyroid tumor cells|
NERI, ANTONINO (Penultimo)
|Parole Chiave:||COPZ1; Cell death; Non-oncogene addiction; Thyroid carcinoma|
|Settore Scientifico Disciplinare:||Settore MED/06 - Oncologia Medica|
|Data di pubblicazione:||1-dic-2017|
|Data ahead of print / Data di stampa:||23-set-2017|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.1016/j.canlet.2017.09.024|
|Appare nelle tipologie:||01 - Articolo su periodico|