دورية أكاديمية

miR-199a and miR-199b facilitate diffuse gastric cancer progression by targeting Frizzled-6

التفاصيل البيبلوغرافية
العنوان: miR-199a and miR-199b facilitate diffuse gastric cancer progression by targeting Frizzled-6
المؤلفون: Soon Auck Hong, Sieun Lee, Jihye Park, Mineui Hong, Jung-Sook Yoon, Heejin Lee, Ji Hyun Lee, Seoree Kim, Hye Sung Won, Keunsoo Kang, Yoon Ho Ko, Young-Ho Ahn
المصدر: Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
بيانات النشر: Nature Portfolio, 2023.
سنة النشر: 2023
المجموعة: LCC:Medicine
LCC:Science
مصطلحات موضوعية: Medicine, Science
الوصف: Abstract Pathological markers that can monitor the progression of gastric cancer (GC) may facilitate the diagnosis and treatment of patients with diffuse GC (DGC). To identify microRNAs (miRNAs) that can differentiate between early and advanced DGC in the gastric mucosa, miRNA expression profiling was performed using the NanoString nCounter method in human DGC tumors. Ectopic expression of miR-199a and miR-199b (miR-199a/b) in SNU601 human GC cells accelerated the growth rate, viability, and motility of cancer cells and increased the tumor volume and weight in a mouse xenograft model. To study their clinicopathological roles in patients with GC, miR-199a/b levels were measured in human GC tumor samples using in situ hybridization. High miR-199a/b expression level was associated with enhanced lymphovascular invasion, advanced T stage, and lymph-node metastasis. Using the 3′-untranslated region (UTR) luciferase assay, Frizzled-6 (FZD6) was confirmed to be a direct target of miR-199a/b in GC cells. siRNA-mediated depletion of FZD6 enhanced the motility of SNU601 cells, and addback of FZD6 restored cancer cell motility stimulated by miR-199a/b. In conclusion, miR-199a/b promotes DGC progression by targeting FZD6, implying that miR-199a/b can be used as prognostic and diagnostic biomarkers for the disease.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2045-2322
Relation: https://doaj.org/toc/2045-2322
DOI: 10.1038/s41598-023-44716-0
URL الوصول: https://doaj.org/article/7c352707d4e4492baf2a44a9660885eb
رقم الأكسشن: edsdoj.7c352707d4e4492baf2a44a9660885eb
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20452322
DOI:10.1038/s41598-023-44716-0