Serum Expression of Seven MicroRNAs in Chronic Lymphocytic Leukemia Patients

作     者：Farzadfard, Ehsan Kalantari, Tahereh Tamaddon, Gholamhossein 

作者机构：Shiraz Univ Med Sci Sch Paramed Sci Shiraz Iran Shiraz Univ Med Sci Sch Paramed Sci Dept Med Biotechnol Shiraz Iran Shiraz Univ Med Sci Sch Paramed Sci Dept Clin Lab Sci Shiraz Iran Shiraz Univ Med Sci Sci & Technol Res Ctr Sch Paramed Sci Diagnost Lab Shiraz Iran 

出 版 物：《JOURNAL OF BLOOD MEDICINE》 (血药杂志)

年 卷 期：2020年第11卷

页      面：97-102页

学科分类：1007[医学-药学(可授医学、理学学位)] 1002[医学-临床医学] 10[医学] 

基　　金：Shiraz University of Medical Sciences [95-01-10-11314] 

主　　题：chronic lymphocytic leukemia circulatory microRNAs noncoding RNA real-time PCR 

摘      要：Purpose: MicroRNAs are small single-strand noncoding RNAs that can be deregulated in a variety of cancers. Over the past few years, multiple markers have been discovered in chronic lymphocytic leukemia (CLL). Among these, miRNAs seem to have important roles in the pathogenesis of CLL. The development and validation of miRNA-expression patterns as bio-markers should have a significant impact in cancer diagnosis, therapeutic success, and increasing the life expectancy of patients. In this study, to specify the utility of circulatory miRNA expression as noninvasive and useful biomarkers for CLL, we analyzed the dysregulation of seven miRNAs: miR30d, miR25-3p, miR19a-3p, miR133b, miR451a, miR145, and miR144 in CLL-patient sera. Methods: Thirty untreated patients with flow-cytometry confirmation of CLL were chosen. Serum samples were collected from 30 newly diagnosed CLL patients. Fifteen healthy samples were taken for comparison as controls. RNAwas extracted using Trizol. RNA from CLL patient specimens was compared to controls with real-time PCR. Results: Seven miRNAs were differently expressed between CLL and normal specimens using the comparative 2(-Delta Delta Ct) method. miRNAs 133b, 25-3p, 451a, 145, 19a-3p, and 144 were overexpressed in sera obtained from CLL patients, and miRNA-30d was under-expressed in patient samples. Among these seven miRNAs, miR19a-3p and miR25-3p showed the most deregulation in CLL patients. Conclusion: Real-time PCR is an applied means to perform high-throughput investigation of serum-RNA samples. We assessed the expression of seven miRNAs in CLL patients by this method. The results demonstrated that the use of miRNA-expression profiling may have an impressive role in the diagnosis of CLL. In addition, miRNA 19a-3p and 25-3p are known oncogenes with therapeutic and potential biomarkers.