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pmid:39156890

Role of glycosylation-related gene MGAT1 in pancreatic ductal adenocarcinoma.

Lai Jiang · Jie Liu · Shengke Zhang · Chenglu Jiang · Jinbang Huang · Haiqing Chen · Xuancheng Zhou · Yiping Fu · Zhongqiu Yang · Rui Wang · Guanhu Yang · Hao Chi · Bo Li

Frontiers in immunology · 2024 doi:10.3389/fimmu.2024.1438935

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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pmid:39156890
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title
Role of glycosylation-related gene MGAT1 in pancreatic ductal adenocarcinoma.
doi
10.3389/fimmu.2024.1438935
pmid
39156890
authors array · 13 items
[0]
Lai Jiang
[1]
Jie Liu
[2]
Shengke Zhang
[3]
Chenglu Jiang
[4]
Jinbang Huang
[5]
Haiqing Chen
[6]
Xuancheng Zhou
[7]
Yiping Fu
[8]
Zhongqiu Yang
[9]
Rui Wang
[10]
Guanhu Yang
[11]
Hao Chi
[12]
Bo Li
journal
Frontiers in immunology
year
2024
abstract
Background: pancreatic ductal adenocarcinoma (PDAC) is a malignant tumor with a very poor prognosis and a complex tumor microenvironment, which plays a key role in tumor progression and treatment resistance. Glycosylation plays an important role in processes such as cell signaling, immune response and protein stability. Materials and methods: single-cell RNA sequencing data and spatial transcriptome data were obtained from GSE197177 and GSE224411, respectively, and RNA-seq data and survival information were obtained from UCSC Xena and TCGA. Multiple transcriptomic data were comprehensively analyzed to explore the role of glycosylation processes in tumor progression, and functional experiments were performed to assess the effects of MGAT1 overexpression on PDAC cell proliferation and migration. Results: In PDAC tumor samples, the glycosylation level of macrophages was significantly higher than that of normal samples. MGAT1 was identified as a key glycosylation-related gene, and its high expression was associated with better patient prognosis. Overexpression of MGAT1 significantly inhibited the proliferation and migration of PDAC cells and affected intercellular interactions in the tumor microenvironment. Conclusion: MGAT1 plays an important role in PDAC by regulating glycosylation levels in macrophages, influencing tumor progression and improving prognosis.MGAT1 is a potential therapeutic target for PDAC and further studies are needed to develop targeted therapeutic strategies against MGAT1 to improve clinical outcomes.
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Non-parametric Wilcoxon rank sum test was used to assess the relationship between two groups of continuous variables. Spearman correlation analysis was used to test the correlation coefficients.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39156890", "kind": "science-record", "revision": 4, "content_hash": "sha256:d7eeb563af9425d5d02d1e2431d283218753643994512c1ce535be0a9a87cb37", "created_at": "2026-11-01T20:29:17Z", "updated_at": "2026-11-01T22:54:59Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Role of glycosylation-related gene MGAT1 in pancreatic ductal adenocarcinoma.", "doi": "10.3389/fimmu.2024.1438935", "pmid": "39156890", "authors": ["Lai Jiang", "Jie Liu", "Shengke Zhang", "Chenglu Jiang", "Jinbang Huang", "Haiqing Chen", "Xuancheng Zhou", "Yiping Fu", "Zhongqiu Yang", "Rui Wang", "Guanhu Yang", "Hao Chi", "Bo Li"], "journal": "Frontiers in immunology", "year": 2024, "abstract": "Background: pancreatic ductal adenocarcinoma (PDAC) is a malignant tumor with a very poor prognosis and a complex tumor microenvironment, which plays a key role in tumor progression and treatment resistance. Glycosylation plays an important role in processes such as cell signaling, immune response and protein stability.\nMaterials and methods: single-cell RNA sequencing data and spatial transcriptome data were obtained from GSE197177 and GSE224411, respectively, and RNA-seq data and survival information were obtained from UCSC Xena and TCGA. Multiple transcriptomic data were comprehensively analyzed to explore the role of glycosylation processes in tumor progression, and functional experiments were performed to assess the effects of MGAT1 overexpression on PDAC cell proliferation and migration.\nResults: In PDAC tumor samples, the glycosylation level of macrophages was significantly higher than that of normal samples. MGAT1 was identified as a key glycosylation-related gene, and its high expression was associated with better patient prognosis. Overexpression of MGAT1 significantly inhibited the proliferation and migration of PDAC cells and affected intercellular interactions in the tumor microenvironment.\nConclusion: MGAT1 plays an important role in PDAC by regulating glycosylation levels in macrophages, influencing tumor progression and improving prognosis.MGAT1 is a potential therapeutic target for PDAC and further studies are needed to develop targeted therapeutic strategies against MGAT1 to improve clinical outcomes.", "claims": [{"id": "claim-method", "statement": "Non-parametric Wilcoxon rank sum test was used to assess the relationship between two groups of continuous variables. 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