LINC01526 Promotes Proliferation and Metastasis of Gastric Cancer by Interacting with TARBP2 to Induce GNG7 mRNA Decay

Gastric cancer is the most common malignancy of the human digestive system. Long noncoding RNAs (lncRNAs) influence the occurrence and development of gastric cancer in multiple ways. However, the function and mechanism of LINC01526 in gastric cancer remain unknown. Herein, we investigated the functi...

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Bibliographic Details
Published in:Cancers 2022-10, Vol.14 (19), p.4940
Main Authors: Zhou, Jin-Yong, Liu, Jin-Yan, Tao, Yu, Chen, Chen, Liu, Shen-Lin
Format: Article
Language:English
Subjects:
Antibodies
Apoptosis
Biomarkers
Biotechnology
Cancer therapies
Cell cycle
Cell growth
Cell migration
Cell proliferation
Complications and side effects
Development and progression
Gastric cancer
Health aspects
HIV
Human immunodeficiency virus
Immunoprecipitation
Lasers
Malignancy
Medical prognosis
Messenger RNA
Metastases
Metastasis
mRNA stability
mRNA turnover
Plasmids
Proteins
Risk factors
RNA-binding protein
Stomach cancer
Therapeutic targets
Tumorigenesis
Xenografts
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Summary:Gastric cancer is the most common malignancy of the human digestive system. Long noncoding RNAs (lncRNAs) influence the occurrence and development of gastric cancer in multiple ways. However, the function and mechanism of LINC01526 in gastric cancer remain unknown. Herein, we investigated the function of LINC01526 with respect to the malignant progression of gastric cancer. We found that LINC01526 was upregulated in gastric cancer cells and tissues. The function experiments in vitro and the Xenograft mouse model in vivo proved that LINC01526 could promote gastric cancer cell proliferation and migration. Furthermore, LINC01526 interacted with TAR (HIV-1) RNA-binding protein 2 (TARBP2) and decreased the mRNA stability of G protein gamma 7 (GNG7) through TARBP2. Finally, the rescue assay showed that downregulating GNG7 partially rescued the cell proliferation inhibited by LINC01526 or TARBP2 silencing. In summary, LINC01526 promoted gastric cancer progression by interacting with TARBP2, which subsequently degraded GNG7 mRNA. This study not only explores the role of LINC01526 in gastric cancer, but also provides a laboratory basis for its use as a new biomarker for diagnosis and therapeutic targets.
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers14194940