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The mir-371a-373 cluster: A crucial miRNA cluster promotes the malignancy of gastric cancer

 Zonglei Mao, Yi Pan, Jiaping Wu, Aizhai Xiang, Kangbei Zhu, Jiayi Li, Jufeng Guo, Ning Tang, Jing Zhang, Jian Liu,  Tao Rui

Abstract:

Gastric cancer is one of the most common and deadliest malignancies worldwide. Better knowledge of the risk factors for gastric cancer is essential for risk classification and therapeutic strategy evolution in gastric cancer patients. Many kinds of miRNA clusters participate in tumorigenesis and tumor progression. Herein, we sought to screen and certify the crucial miRNA cluster for prognosis prediction and potential therapeutic targets in gastric cancer. The results showed that the mir-371a-373 cluster was the most highly expressed miRNA cluster in gastric cancer. The high expression of the mir-371a-373 cluster (mir-371a, mir-372, and mir-373) was positively associated with the poor overall survival of gastric cancer patients. The expression of mir-373 was correlated with early gastric cancer recurrence. mir-373 was an independent risk factor for gastric cancer recurrence and mortality. Then, gain- and loss-of-function experiments demonstrated that mir-373 could promote the malignancy of gastric cancer cells in vitro and in vivo. Through bioinformatics analysis and experimental validation, mir-373 was correlated with tumor regulation, and ZFP91 was the direct target of mir-373. Our findings suggest that the miR-371-373 cluster, especially mir-373, could be a robust marker for the prognosis prediction of gastric cancer and a potential therapeutic target for gastric cancer.

Received date: 05/26/2025

Accepted date: 09/15/2025

Ahead of print publish date: 09/29/2025

Keywords: gastric cancer, miRNA cluster, ZFP91, prognosis

Supplementary files:
N220 Supplementary Tables and Figures-TE1.docx
N220 Supplementary material A-Expression levels of pre-miRNAs in gastric cancers and non-tumors.xlsx
N220 Supplementary material B-Differential expressed pre-miRNAs in gastric cancer.xlsx

DOI: doi:10.4149/neo_2025_250526N220

Pubmed

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