NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE133058 Query DataSets for GSE133058
Status Public on Apr 10, 2020
Title hsa_circ_0007841: A novel potential biomarker and drug resistance for multiple myeloma
Organism Homo sapiens
Experiment type Non-coding RNA profiling by array
Summary Purpose:It has been shown that circular RNA (circRNA) is a key regulatory factor in development and progression of human tumors. However, the working mechanism and clinical significance of most circRNAs remain unknown in human cancer, including multiple myeloma (MM), a hematologic malignancy. Patients and methods:In the present study, high-throughput circRNA microarray was combined with bioinformatics to identify differentially expressed circRNAs in MM. The hsa_circ_0007841 expressions were shown in MM tissues of 86 patients and drug-resistant cell lines and pathological features were detected. Further, the relationship between hsa_circ_0007841 expressions in the MM tissues and pathological features of MM patients were discussed. The role of hsa_circ_0007841 as a potential biomarker and therapeutic target was analyzed. Results:Our results indicated that in MM tissues collected from patients, MM cell lines and drug-resistant cell lines, the hsa_circ_0007841 expression was significantly upregulated. A close connection with prognosis was observed. That is, hsa_circ_0007841 upregulation was correlated with chromosomal aberrations, such as gain 1q21, t(4:14) and mutations in ATR and IRF4 genes. This finding was further verified in large samples. Finally, bioinformatics analysis indicated interaction that 8 differentially expressed miRNAs and 10 candidate mRNAs interacted with hsa_circ_0007841. These results sheds new light on the basic functional research in the future. Conclusion:It was reported for the first time that hsa_circ_0007841 was significantly upregulated in MM. Our study indicated that hsa_circ_0007841 may be a novel biomarker for MM and involved in the progression of MM.
 
Overall design the bone marrow samples from 3 MM patients were sorted by magnetic activated cell sorting (MACS) using anti-CD138 MicroBeads, and the plasma cells were enriched.
 
Contributor(s) Gao M, Xiao H, Hang D, Jiang S, Fu Y, Gong L
Citation(s) 31803627
Submission date Jun 20, 2019
Last update date Apr 10, 2020
Contact name FU YUN FENG
E-mail(s) 14579@qq.com
Phone 13786450644
Organization name The Third Xiangya Hospital of Central South University
Department Blood
Lab Blood
Street address No. 138 Tonglu Road, Yuelu District, Hexi Distric
City CHANG SHA
State/province HUNAN
ZIP/Postal code 410000
Country China
 
Platforms (1)
GPL21825 074301 Arraystar Human CircRNA microarray V2
Samples (6)
GSM3899189 Patient 1 A1_gzhx
GSM3899190 Patient 2 A2_chchl
GSM3899191 Patient 3 A3_hlm
Relations
BioProject PRJNA549859

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE133058_RAW.tar 4.2 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap