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Updated: Oct 20, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
CircITGA7 Suppresses Gastric Cancer Progression Through miR-1471/MTDH Axis
Haifeng Jin1, Zheng Wu2, Bibo Tan3
1Department of Gastroenterology, The 980th Hospital of the PLA Joint Logistics Support Force (Primary Bethune International Peace Hospital of PLA), Shijiazhuang, China.
Abstract:
In recent years, there have been reports about the involvement of circular RNAs (circRNAs) in the pathogenesis of gastric cancer (GC), but the molecular mechanism in cell proliferation, invasion, and migration is still unclear. Based on The Cancer Genome Atlas (TCGA) database, we analyzed differentially expressed circRNAs between GC and non-tumor tissues. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis were used to clarify the functional role in GC. Here, we showed that circITGA7 was lowly expressed in GC tissues based on the TCGA database. In vitro, silencing the expression of circITGA7 increased cell proliferation and metastasis, whereas overexpression did the opposite. Mechanistically, miR-1471 has circITGA7 as a sponge, and miR-1471 has metadherin (MTDH) as a target gene. Consequently, functional analysis showed that the tumor suppressor effect of circITGA7 was the result of regulating the miR-1471/MTDH axis. Overall, the circITGA7/miR-1471/MTDH signaling pathway may play a crucial role in GC, providing a new potential mechanism involved in GC progression.
Insights
Circular RNAs (circRNAs) like circITGA7 are involved in gastric cancer (GC) progression. This study reveals circITGA7 acts as a tumor suppressor by regulating the circITGA7/miR-1471/MTDH axis in GC.
Area of Science:
- Oncology
- Molecular Biology
- Genomics
Background:
- Circular RNAs (circRNAs) are increasingly implicated in gastric cancer (GC) pathogenesis.
- The precise molecular mechanisms underlying circRNA involvement in GC cell proliferation, invasion, and migration remain largely undefined.
Purpose of the Study:
- To investigate the role of differentially expressed circRNAs in gastric cancer.
- To elucidate the molecular mechanism of circITGA7 in GC progression.
Main Methods:
- Analysis of The Cancer Genome Atlas (TCGA) database for differentially expressed circRNAs in GC.
- Gene Ontology and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis.
- In vitro experiments involving circITGA7 silencing and overexpression, and investigation of the miR-1471/metadherin (MTDH) axis.
Main Results:
- circITGA7 was found to be downregulated in GC tissues.
- Silencing circITGA7 enhanced GC cell proliferation and metastasis; overexpression inhibited these processes.
- circITGA7 functions as a sponge for miR-1471, which targets metadherin (MTDH).
- The tumor suppressive effect of circITGA7 is mediated through the regulation of the miR-1471/MTDH axis.
Conclusions:
- The circITGA7/miR-1471/MTDH signaling pathway plays a significant role in gastric cancer progression.
- circITGA7 represents a potential therapeutic target and biomarker for GC.
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