MicroRNA-34a Alleviates Gemcitabine Resistance in Pancreatic Cancer by Repression of Cancer Stem Cell Renewal

التفاصيل البيبلوغرافية
العنوان: MicroRNA-34a Alleviates Gemcitabine Resistance in Pancreatic Cancer by Repression of Cancer Stem Cell Renewal
المؤلفون: Ge Gao, Jianzhou Liu, Ning Li, Yue Pan, Xufeng Tao, Qing Chen, Kun Li, Junchao Guo, Gary Guishan Xiao, Yongxin Zhao, Vay Liang W. Go
المصدر: Pancreas. 50:1260-1266
بيانات النشر: Ovid Technologies (Wolters Kluwer Health), 2021.
سنة النشر: 2021
مصطلحات موضوعية: Antimetabolites, Antineoplastic, Epithelial-Mesenchymal Transition, Cell Survival, Endocrinology, Diabetes and Metabolism, Cell, Mice, Nude, Deoxycytidine, Endocrinology, Cell Movement, Cancer stem cell, Cell Line, Tumor, Pancreatic cancer, Internal Medicine, medicine, Animals, Humans, Viability assay, Cell Self Renewal, Receptor, Notch1, Notch 1, Hepatology, Chemistry, medicine.disease, Xenograft Model Antitumor Assays, Gemcitabine, Gene Expression Regulation, Neoplastic, Pancreatic Neoplasms, MicroRNAs, medicine.anatomical_structure, Drug Resistance, Neoplasm, MicroRNA 34a, Cancer research, Stem cell, Carcinoma, Pancreatic Ductal, Signal Transduction, medicine.drug
الوصف: OBJECTIVES This study aimed to enhance the sensitivity of pancreatic ductal adenocarcinoma cells by microRNA-34a (miR-34a)-mediated targeting of Notch 1. METHODS Cell viability was determined by using an MTT (3-(4,5)-dimethylthiahiazo(-2)-3,5-diphenytetrazoliumromide) assay. The expression levels of miR-34a and relevant mRNAs were determined using quantitative polymerase chain reaction. Protein levels were measured by Western blotting. Cellular stemness was assessed by cell invasiveness and sphere formation assays. A transplanted tumor model was established for in vivo experiments. RESULTS MicroRNA-34a enhanced gemcitabine sensitivity both in vivo and in vitro. MicroRNA-34a suppressed the stemness and proliferation of pancreatic cancer stem cells. MicroRNA-34a directly associated with Notch 1, which lies upstream of epithelial-mesenchymal transition signaling pathways. CONCLUSIONS MicroRNA-34a sensitized pancreatic cancer cells to gemcitabine treatment by inhibiting Notch 1 signaling in pancreatic cancer stem cells, indicating that miR-34a has the potential to be developed as a novel therapeutic agent for the treatment of gemcitabine-resistant pancreatic ductal adenocarcinoma cells.
تدمد: 1536-4828
0885-3177
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc44b31821a21c258b90fdd84d36e314Test
https://doi.org/10.1097/mpa.0000000000001920Test
رقم الانضمام: edsair.doi.dedup.....fc44b31821a21c258b90fdd84d36e314
قاعدة البيانات: OpenAIRE