Extracellular vesicles released by mesenchymal-like prostate carcinoma cells modulate EMT state of recipient epithelial-like carcinoma cells through regulation of AR signaling

التفاصيل البيبلوغرافية
العنوان: Extracellular vesicles released by mesenchymal-like prostate carcinoma cells modulate EMT state of recipient epithelial-like carcinoma cells through regulation of AR signaling
المؤلفون: Alexandre de la Taille, Pascale Maillé, Guido Jenster, Virginie Firlej, Damien Destouches, Stéphane Terry, Ihsan Y. El-Sayed, Francis Vacherot, Enis Kostallari, Ahmad Daher, Raghida Abou Merhi, Nathaline Haidar-Ahmad, Eric Huet
المساهمون: Urology
المصدر: Cancer Letters, 410, 100-111. Elsevier Ireland Ltd
سنة النشر: 2017
مصطلحات موضوعية: 0301 basic medicine, Male, Cancer Research, Epithelial-Mesenchymal Transition, Neoplasms, Hormone-Dependent, Time Factors, Antineoplastic Agents, Hormonal, Biology, Transforming Growth Factor beta1, 03 medical and health sciences, Prostate cancer, chemistry.chemical_compound, 0302 clinical medicine, Cell Movement, Cell-Derived Microparticles, Cell Line, Tumor, medicine, Carcinoma, Tumor Microenvironment, Enzalutamide, Humans, Neoplasm Invasiveness, Dose-Response Relationship, Drug, Mesenchymal stem cell, Cancer, Prostatic Neoplasms, Androgen Antagonists, medicine.disease, Androgen receptor, 030104 developmental biology, Phenotype, Oncology, chemistry, Drug Resistance, Neoplasm, Receptors, Androgen, 030220 oncology & carcinogenesis, Immunology, Cancer cell, Cancer research, Signal transduction, Signal Transduction
الوصف: Extracellular vesicles released from cancer cells may play an important role in cancer progression by shuttling oncogenic information into recipient cells. However, our knowledge is still fragmentary and there remain numerous questions regarding the mechanisms at play and the functional consequences of these interactions. We have recently established a mesenchymal-like prostate cancer cell line (22Rv1/CR-1; Mes-PCa). In this study, we assessed the effects of the extracellular vesicles released by these cells on recipient androgen-dependent epithelial VCaP prostate cancer cells. Mes-PCa derived vesicles were found to promote mesenchymal features in the recipient epithelial-like prostate cancer cells. This transformation was accompanied by a modulation of androgen receptor signaling and activation of TGFβ signaling pathway. Moreover, recipient cells acquiring mesenchymal traits displayed enhanced migratory and invasive features as well as increased resistance to the androgen receptor antagonist, enzalutamide. Our results suggest a previously unappreciated role for Mes-PCa secreted vesicles in cancer promotion by transferring cell-mediated signals and promoting phenotypic changes in recipient prostate cancer cells.
تدمد: 0304-3835
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b943d4d11c0eebc47c15f2f1c5c5a89Test
https://hdl.handle.net/1765/108564Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....3b943d4d11c0eebc47c15f2f1c5c5a89
قاعدة البيانات: OpenAIRE