The cytoskeleton actin binding protein filamin A impairs both IGF2 mitogenic effects and the efficacy of IGF1R inhibitors in adrenocortical cancer cells

التفاصيل البيبلوغرافية
العنوان: The cytoskeleton actin binding protein filamin A impairs both IGF2 mitogenic effects and the efficacy of IGF1R inhibitors in adrenocortical cancer cells
المؤلفون: Michaela Luconi, Massimo Mannelli, Andreea Liliana Serban, Rosa Catalano, Donatella Treppiedi, Francesca Elli, Erika Peverelli, Giovanna Mantovani, Anna Spada, Valentina Morelli, Elena Giardino, Maura Arosio, Federica Mangili
المصدر: Cancer letters. 497
سنة النشر: 2020
مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Linsitinib, medicine.medical_treatment, Filamins, Apoptosis, Filamin, Receptor, IGF Type 1, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Insulin-Like Growth Factor II, medicine, Adrenocortical Carcinoma, Biomarkers, Tumor, Tumor Cells, Cultured, Gene silencing, FLNA, Humans, Pyrroles, Autocrine signalling, Insulin-like growth factor 1 receptor, Cell Proliferation, Cell growth, Growth factor, Imidazoles, Adrenal Cortex Neoplasms, Receptor, Insulin, body regions, Gene Expression Regulation, Neoplastic, Actin Cytoskeleton, 030104 developmental biology, adrenocortical carcinoma, growth factors, cytoskeleton, linsitinib, NVP-ADW742, Pyrimidines, Oncology, chemistry, 030220 oncology & carcinogenesis, Pyrazines, Cancer research, Mitogens, Adrenocortical carcinoma, Cytoskeleton, Growth factors, Signal Transduction
الوصف: Adrenocortical carcinomas (ACCs) overexpress insulin-like growth factor 2 (IGF2), that drives a proliferative autocrine loop by binding to IGF1R and IR, but IGF1R/IR-targeted therapies failed in ACC patients. The cytoskeleton actin-binding protein filamin A (FLNA) impairs IR signalling in melanoma cells. Aims of this study were to test FLNA involvement in regulating IGF1R and IR responsiveness to both IGF2 and inhibitors in ACC. In ACC cells H295R and SW13 and primary cultures (1ACC, 4 adenomas) we found that IGF1R and IR interacted with FLNA, and FLNA silencing increased IGF1R and reduced IR expression, with a downstream effect of increased cell proliferation and ERK phosphorylation. In addition, FLNA knockdown potentiated antiproliferative effects of IGF1R/IR inhibitor Linsitinib and IGF1R inhibitor NVP-ADW742 in H295R. Finally, Western blot showed lower FLNA expression in ACCs (n = 10) than in ACAs (n = 10) and an inverse correlation of FLNA/IGF1R ratio with ERK phosphorylation in ACCs only. In conclusion, we demonstrated that low FLNA levels enhance both IGF2 proliferative effects and IGF1R/IR inhibitors efficacy in ACC cells, suggesting FLNA as a new factor influencing tumor clinical behavior and the response to the therapy with IGF1R/IR-targeted drugs.
تدمد: 1872-7980
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b6e4184d062de5492bf009f17dbf51d
https://pubmed.ncbi.nlm.nih.gov/33075426
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....7b6e4184d062de5492bf009f17dbf51d
قاعدة البيانات: OpenAIRE