Abstract | AIM: METHODS: We used fluorescence-activated cell sorting and Hoechst 33342 labeling to obtain SP cells from the human gastric carcinoma cell line MKN-45. The miRNA expression profiles of the SP and major population (MP) cells were examined using a miRNA gene chip, and key miRNAs were obtained according to aberrant expression and the miRNAs' possible targets as predicted by bioinformatics. RESULTS: Using a significance criterion of a 1.5-fold or greater difference in expression level, we observed an increase in the expression of 34 miRNAs and a decrease in the expression of 34 miRNAs when comparing SP to MP cells. Using quantitative real-time reverse transcription-polymerase chain reaction to test for differentially expressed miRNAs combined with bioinformatics results, we found that the downregulated miRNAs, such as hsa-miR-3175 and hsa-miR-203, and the upregulated miRNAs, including hsa-miR-130a, hsa-miR-324-5p, hsa-miR-34a, and hsa-miR-25-star, may be important in maintaining and regulating the characteristics of SP cells. CONCLUSION:
|
Authors | Hai-Hong Zhang, Guo-Li Gu, Xiang-Yang Zhang, Feng-Zhi Li, Li Ding, Qin Fan, Ran Wu, Wei Shi, Xin-Yan Wang, Lin Chen, Xue-Ming Wei, Xiao-Ying Yuan |
Journal | World journal of gastroenterology
(World J Gastroenterol)
Vol. 21
Issue 12
Pg. 3519-26
(Mar 28 2015)
ISSN: 2219-2840 [Electronic] United States |
PMID | 25834316
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
|
Topics |
- Adenocarcinoma
(genetics, metabolism, pathology)
- Cell Line, Tumor
- Computational Biology
- Gene Expression Profiling
(methods)
- Gene Expression Regulation, Neoplastic
- Humans
- MicroRNAs
(genetics, metabolism)
- Oligonucleotide Array Sequence Analysis
- Real-Time Polymerase Chain Reaction
- Reverse Transcriptase Polymerase Chain Reaction
- Side-Population Cells
(metabolism, pathology)
- Stomach Neoplasms
(genetics, metabolism, pathology)
|