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Updated: Dec 27, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Long noncoding RNA TRPM2-AS acts as a microRNA sponge of miR-612 to promote gastric cancer progression and
Jian Xiao1, Linling Lin1, Dakui Luo2
1Department of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, China.
Abstract:
Long noncoding RNAs (lncRNAs) are emerging as important regulators of tumorigenesis and are frequently dysregulated in cancers. Here, we identify a critical lncRNA TRPM2-AS which is aberrantly expressed in gastric cancer (GC) tissues by screening The Cancer Genome Atlas Program(TCGA) database of GC cohort, and its upregulation is clinically associated with advanced pathologic stages and poor prognosis in GC patients. Silencing TRPM2-AS inhibits the proliferation, metastasis and radioresistance of GC cell whereas ectopic expression of TRPM2-AS significantly improves the progression of GC cell in multiple experiments. Mechanistically, TRPM2-AS serves as a microRNA sponge or a competitive endogenous RNA (ceRNA) for tumor suppressive microRNA miR-612 and consequently modulates the derepression of IGF2BP1 and FOXM1. Moreover, induced upregulation of IGF2BP1 subsequently increases the expression of c-Myc and promotes GC cell progression. Meanwhile, TRPM2-AS promotes the radioreistance of GC cell through enhancing the expression of FOXM1 as well. Thus, our findings support a new regulatory axis between TRPM2-AS, miR-612, IGF2BP1, or FOXM1 which serve as crucial effectors in GC tumorigenesis and malignant development, suggesting a promising therapeutic and diagnostic direction for GC.
Insights
Long noncoding RNA TRPM2-AS promotes gastric cancer (GC) progression and radioresistance. Targeting TRPM2-AS may offer new therapeutic strategies for GC patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long noncoding RNAs (lncRNAs) are key regulators in tumorigenesis.
- Dysregulation of lncRNAs is common in various cancers, including gastric cancer (GC).
Purpose of the Study:
- Identify critical lncRNAs in GC.
- Investigate the role and mechanism of TRPM2-AS in GC progression and radioresistance.
Main Methods:
- Screened The Cancer Genome Atlas Program (TCGA) database for lncRNA expression in GC.
- Performed in vitro experiments to assess the functional impact of TRPM2-AS.
- Utilized microRNA sponge assays to elucidate the molecular mechanism.
Main Results:
- TRPM2-AS is upregulated in GC tissues and associated with advanced stages and poor prognosis.
- TRPM2-AS silencing inhibits GC cell proliferation, metastasis, and radioresistance.
- TRPM2-AS acts as a ceRNA for miR-612, upregulating IGF2BP1 and FOXM1, promoting GC progression and radioresistance.
Conclusions:
- TRPM2-AS, miR-612, IGF2BP1, and FOXM1 form a regulatory axis crucial for GC tumorigenesis.
- TRPM2-AS represents a potential diagnostic biomarker and therapeutic target for GC.
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