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Published on: December 1, 2023
Long Noncoding RNA LINC01234 Functions as a Competing Endogenous RNA to Regulate CBFB Expression by Sponging
Xin Chen1, Zhenyao Chen1, Shanxun Yu1
1Department of Oncology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Abstract:
Purpose: Long noncoding RNAs (lncRNAs) have emerged as important regulators in a variety of human diseases, including cancers. However, the overall biological roles and clinical significance of most lncRNAs in gastric carcinogenesis are not fully understood. We investigated the clinical significance, biological function, and mechanism of LINC01234 in gastric cancer.Experimental Design: First, we analyzed LINC01234 alterations in gastric cancerous and noncancerous tissues through an analysis of sequencing data obtained from The Cancer Genome Atlas. Next, we evaluated the effect of LINC01234 on the gastric cancer cell proliferation and apoptosis, and its regulation of miR-204-5p by acting as a competing endogenous RNA (ceRNA). The animal model was used to support the in vitro experimental findings.Results: We found that LINC01234 expression was significantly upregulated in gastric cancer tissues and was associated with larger tumor size, advanced TNM stage, lymph node metastasis, and shorter survival time. Furthermore, knockdown of LINC01234-induced apoptosis and growth arrest in vitro and inhibited tumorigenesis in mouse xenografts. Mechanistic investigations indicated that LINC01234 functioned as a ceRNA for miR-204-5p, thereby leading to the derepression of its endogenous target core-binding factor β (CBFB).Conclusions: LINC01234 is significantly overexpressed in gastric cancer, and LINC01234-miR-204-5p-CBFB axis plays a critical role in gastric cancer tumorigenesis. Our findings may provide a potential new target for gastric cancer diagnosis and therapy. Clin Cancer Res; 24(8); 2002-14. ©2018 AACR.
Insights
Long noncoding RNA LINC01234 is highly expressed in gastric cancer, promoting tumor growth and metastasis. Targeting the LINC01234-miR-204-5p-CBFB pathway offers a potential strategy for gastric cancer diagnosis and treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long noncoding RNAs (lncRNAs) are key regulators in human diseases, including cancer.
- The roles of most lncRNAs in gastric cancer development remain unclear.
- Investigating specific lncRNAs like LINC01234 is crucial for understanding gastric carcinogenesis.
Purpose of the Study:
- To determine the clinical significance and biological function of LINC01234 in gastric cancer.
- To elucidate the underlying molecular mechanism of LINC01234 in gastric cancer.
- To explore LINC01234 as a potential diagnostic and therapeutic target.
Main Methods:
- Analysis of The Cancer Genome Atlas (TCGA) data for LINC01234 expression in gastric tissues.
- In vitro studies assessing the impact of LINC01234 on gastric cancer cell proliferation and apoptosis.
- Investigation of LINC01234's role as a competing endogenous RNA (ceRNA) for miR-204-5p.
- In vivo validation using a mouse xenograft model.
Main Results:
- LINC01234 was significantly upregulated in gastric cancer tissues.
- High LINC01234 expression correlated with advanced tumor stage, metastasis, and poor prognosis.
- LINC01234 knockdown inhibited tumor growth and induced apoptosis in vitro and in vivo.
- LINC01234 acts as a ceRNA, sponging miR-204-5p and derepressing its target, CBFB.
Conclusions:
- LINC01234 is a critical oncogene in gastric cancer.
- The LINC01234-miR-204-5p-CBFB axis is a key driver of gastric cancer progression.
- LINC01234 represents a promising novel biomarker and therapeutic target for gastric cancer.
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