4.7 Article

Bioinformatics identification of potentially involved microRNAs in Tibetan with gastric cancer based on microRNA profiling

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CANCER CELL INTERNATIONAL
卷 15, 期 -, 页码 -

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BMC
DOI: 10.1186/s12935-015-0266-1

关键词

Gastric cancer; miRNA microarray; Differentially expressed miRNAs; Enrichment analysis; Network of miRNAs-targets

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资金

  1. Scientific research project funds of Qinghai department [2014-ZJ-737]
  2. Qinghai-Utah Joint Research Key Lab for High Altitude Medicine [2014-ZJ-Y39]

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Objective: The incidence of gastric cancer is high in Chinese Tibetan. This study aimed to identify the differentially expressed microRNAs (miRNAs) and further explore their potential roles in Tibetan with gastric cancer so as to predict potential therapeutic targets. Methods: A total of 10 Tibetan patients (male: female = 6: 4) with gastric cancer were enrolled for isolation of matched gastric cancer and adjacent non-cancerous tissue samples. Affymetrix GeneChip microRNA 3.0 Array was employed for detection of miRNA expression in samples. Differential expression analysis between two sample groups was analyzed using Limma package. Then, MultiMiR package was used to predict targets for miRNAs. Following, the target genes were put into DAVID (Database for Annotation, Visualization and Integrated Discovery) to identify the significant pathways of miRNAs. Results: Using Limma package in R, a total of 27 differentially expressed miRNAs were screened out in gastric cancer, including 25 down-regulated (e.g. hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p) and 2 up-regulated miRNAs. According to multiMiR package, a number of 1445 target genes (e.g. Wnt1, KLF4 and S1PR1) of 13 differentially expressed miRNAs were screened out. Among those miRNAs, hsa-miR-148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p were identified with the most target genes. Furthermore, three miRNAs were significantly enriched in numerous common cancer-related pathways, including Wnt signaling pathway, MAPK signaling pathway and Jak-STAT signaling pathway. Conclusions: The present study identified a downregulation and enrichment in cancer-related pathways of hsa-miR148a-3p, hsa-miR-148b-3p and hsa-miR-363-3p in Tibetan with gastric cancer, which can be suggested as therapeutic targets.

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