MSI1 Promotes the Expression of the GBM Stem Cell Marker CD44 by Impairing miRNA-Dependent Degradation

التفاصيل البيبلوغرافية
العنوان: MSI1 Promotes the Expression of the GBM Stem Cell Marker CD44 by Impairing miRNA-Dependent Degradation
المؤلفون: Jacob Haase, Rebecca Pötschke, Luiz O. F. Penalva, Sebastian Simmermacher, Claudia Misiak, Markus Glaß, Stefan Hüttelmaier, Caspar D. Kühnöl
المصدر: Cancers
Volume 12
Issue 12
Cancers, Vol 12, Iss 3654, p 3654 (2020)
بيانات النشر: MDPI, 2020.
سنة النشر: 2020
مصطلحات موضوعية: 0301 basic medicine, Cancer Research, MSI1, cancer stem cell, recurrence, Cell, Stem cell marker, urologic and male genital diseases, lcsh:RC254-282, GBM, Article, 03 medical and health sciences, 0302 clinical medicine, Downregulation and upregulation, Cancer stem cell, microRNA, medicine, Progenitor cell, CD44, luteolin, miRNA, biology, urogenital system, Neurogenesis, glioblastoma, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, nervous system diseases, 030104 developmental biology, medicine.anatomical_structure, Musashi1, Oncology, 030220 oncology & carcinogenesis, Cancer research, biology.protein
الوصف: The stem cell marker Musashi1 (MSI1) is highly expressed during neurogenesis and in glioblastoma (GBM). MSI1 promotes self-renewal and impairs differentiation in cancer and non-malignant progenitor cells. However, a comprehensive understanding of its role in promoting GBM-driving networks remains to be deciphered. We demonstrate that MSI1 is highly expressed in GBM recurrences, an oncologist&rsquo
s major defiance. For the first time, we provide evidence that MSI1 promotes the expression of stem cell markers like CD44, co-expressed with MSI1 within recurrence-promoting cells at the migrating front of primary GBM samples. With GBM cell models of pediatric and adult origin, including isolated primary tumorspheres, we show that MSI1 promotes stem cell-like characteristics. Importantly, it impairs CD44 downregulation in a 3&prime
UTR- and miRNA-dependent manner by controlling mRNA turnover. This regulation is disturbed by the previously reported MSI1 inhibitor luteolin, providing further evidence for a therapeutic target potential of MSI1 in GBM treatment.
وصف الملف: application/pdf
اللغة: English
تدمد: 2072-6694
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3c7e571a2ca1edde1451616dec3767bTest
http://europepmc.org/articles/PMC7762192Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....e3c7e571a2ca1edde1451616dec3767b
قاعدة البيانات: OpenAIRE