دورية أكاديمية

Loss of RANBP3L leads to transformation of renal epithelial cells towards a renal clear cell carcinoma like phenotype

التفاصيل البيبلوغرافية
العنوان: Loss of RANBP3L leads to transformation of renal epithelial cells towards a renal clear cell carcinoma like phenotype
المؤلفون: Chernyakov, Dmitry, Groß, Alexander, Fischer, Annika, Bornkessel, Nicola, Schultheiss, Christoph, Gerloff, Dennis, Edemir, Bayram
المصدر: http://lobid.org/resources/99370679188706441Test#!, 40(1):226.
سنة النشر: 2021
المجموعة: Publisso (ZB MED-Publikationsportal Lebenswissenschaften)
مصطلحات موضوعية: Cell Line, Tumor [MeSH], Disease Progression [MeSH], Kidney Neoplasms/metabolism [MeSH], Kidney Neoplasms/pathology [MeSH], Epithelial Cells/metabolism [MeSH], Transfection [MeSH], Renal cell carcinoma, Kidney Neoplasms/genetics [MeSH], Phenotype [MeSH], Epithelial Cells/pathology [MeSH], Carcinoma, Renal Cell/genetics [MeSH], Tumor progression, Humans [MeSH], Nucleocytoplasmic Transport Proteins/genetics [MeSH], Animals [MeSH], Tumor suppressor, Mice, Knockout [MeSH], Renal Cell/metabolism [MeSH], Mice [MeSH], CRISPR/Cas9, Research, HEK293 Cells [MeSH], Prognosis [MeSH], Hyperosmolality, Nucleocytoplasmic Transport Proteins/metabolism [MeSH], Renal Cell/pathology [MeSH]
الوصف: Background!#!Renal cell carcinomas (RCC) are characterized by the deregulation of several hundred hyperosmolality-responsive genes. High expression of a subset of these genes including the Ran binding protein 3 like (RANBP3L) is linked to a favorable prognostic outcome in RCC. However, the cellular function of RANBP3L remains largely unknown.!##!Methods!#!We used CRISPR/Cas9-mediated gene editing to generate functional deletions of the Ranbp3l and nuclear factor of activated T cells 5 (Nfat5) gene loci in a murine renal cell line. The NFAT5-KO cells were used to assess the regulation of Ranbp3l by NFAT5 using immunofluorescence, RNA-Seq and promoter assays. RANBP3L-deficient cells were analyzed for changes in cell morphology, proliferation, migration and colony-forming capacity using immunofluorescence and live cell imaging. RANPB3L-dependent changes in gene expression were identified by RNA-Seq.!##!Results!#!We show that NFAT5 directly regulates Ranpb3l under hyperosmotic conditions by binding its promoter. Functional analysis of RANBP3L-deficient cells revealed a loss of epithelial structure, an increased cell migration behavior and colony forming capacity, accompanied by massive alterations in gene expression, all of which are hallmarks for tumor cells. Strikingly, a RANBP3L dependent signature of 60 genes separated samples with clear cell carcinoma (KIRC) from papillary (KIRP), chromophobe renal carcinoma (KICH) and healthy tissue.!##!Conclusions!#!Loss of RANBP3L induces a tumor like phenotype resembles RCC, especially KIRC, on the morphological and gene expression level and might promote tumor development and progression. Therapeutic reconstitution or elevation of osmoregulated RANBP3L expression might represent a novel treatment strategy for RCC or KIRC.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: https://repository.publisso.de/resource/frl:6463827Test; https://doi.org/10.1186/s13046-021-01982-yTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265145Test/
DOI: 10.1186/s13046-021-01982-y
الإتاحة: https://doi.org/10.1186/s13046-021-01982-yTest
https://repository.publisso.de/resource/frl:6463827Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265145Test/
حقوق: https://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.84751936
قاعدة البيانات: BASE