FTO promotes gastric cancer progression by modulating MAP4K4 expression via demethylation in an m6A-dependent manner

• Published in: Medical oncology (Northwood, London, England) London, England), 2024-04, Vol.41 (5), p.120-120, Article 120
• Main Authors: Yin, Zhe, Guo, Xiong, Liang, Xiaolong, Wang, Ziwei
• Format: Article
• Language: English
• Subjects: Adenine; Alpha-Ketoglutarate-Dependent Dioxygenase FTO - genetics; Alpha-Ketoglutarate-Dependent Dioxygenase FTO - metabolism; Demethylation; Gastric cancer; Gene Expression Regulation, Neoplastic; Hematology; Humans; Internal Medicine; Intracellular Signaling Peptides and Proteins - metabolism; Medicine; Medicine & Public Health; Oncology; Original Paper; Pathology; Prognosis; Protein Serine-Threonine Kinases - metabolism; Stomach Neoplasms - pathology
• ISSN: 1559-131X; 1357-0560; 1559-131X
• DOI: 10.1007/s12032-024-02369-7

Gastric cancer (GC) is a serious malignant tumour with a high mortality rate and a poor prognosis. Recently, emerging evidence has suggested that N6-methyladenosine (m6A) modification plays a crucial regulatory role in cancer progression. However, the exact role of m6A regulatory factors FTO in GC is unclear. First, the expression of m6A methylation-related regulatory factors in clinical samples and the clinical data of the corresponding patients were obtained from The Cancer Genome Atlas (TCGA-STAD) dataset, and correlation analysis between FTO expression and patient clinicopathological parameters was subsequently performed. qRT-PCR, immunohistochemistry (IHC) and western blotting (WB) were used to verify FTO expression in GC. CCK-8, EdU, flow cytometry and transwell assays were used to evaluate the effect of FTO on the behaviour of GC cells. Transcriptome sequencing and RNA immunoprecipitation analysis were used to explore the potential regulatory mechanisms mediated by FTO. FTO was highly expressed in GC tissues and cells, and high expression of FTO predicted a worse prognosis than low expression. Functionally, overexpression of FTO promoted the proliferation, migration and invasion of GC cells but inhibited cell apoptosis. Mechanistically, we found that FTO is upregulated in GC and promotes GC progression by modulating the expression of MAP4K4. Taken together, our findings provide new insights into the effects of FTO-mediated m6A demethylation and could lead to the development of new strategies for GC monitoring and aggressive treatment.