Evidence map›Paper›PMID 41050213›Full record

ArticleGlobal medical genetics2025

Identification of novel high-risk genes in gastric cancer through single-cell RNA sequencing, eQTL Mendelian randomization, and in vitro validation.

Li Qi, Haoyu Chen, Xinyu Hao, Tianyu Gao, Pingping Zhou, Wenbo Li, Chen Wang, Kunfeng Li, Shaowei Liu, Yuhua Wang and 4 more

Abstract read
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Article in Global medical genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Li QiSchool of Graduate, Hebei University of Chinese Medicine, Shijiazhuang 050091, China.
Haoyu ChenSchool of Graduate, Hebei University of Chinese Medicine, Shijiazhuang 050091, China.
Xinyu HaoDepartment of Pharmacy, Peking University Third Hospital, Beijing 100191, China.
Tianyu GaoSchool of Graduate, Hebei University of Chinese Medicine, Shijiazhuang 050091, China.
Pingping ZhouDepartment of Gastroenterology, Hebei Province Hospital of Chinese Medicine, Shijiazhuang 050011, China.
Wenbo LiSchool of Graduate, Hebei University of Chinese Medicine, Shijiazhuang 050091, China.
Chen WangDepartment of Gastroenterology, Beijing University of Chinese Medicine Third Affiliated Hospital, Beijing 100029, China.
Kunfeng LiDepartment of Gastroenterology, Beijing University of Chinese Medicine Third Affiliated Hospital, Beijing 100029, China.
Shaowei LiuDepartment of Gastrointestinal Surgery, The First Hospital of Hebei Medical University, Shijiazhuang 050023, China.
Yuhua WangSchool of Graduate, Hebei University of Chinese Medicine, Shijiazhuang 050091, China.
Xuetong RenSchool of Graduate, Hebei University of Chinese Medicine, Shijiazhuang 050091, China.
Haiyan BaiDepartment of Gastroenterology, Hebei Province Hospital of Chinese Medicine, Shijiazhuang 050011, China.
Ningning RenDepartment of Gastroenterology, Beijing University of Chinese Medicine Third Affiliated Hospital, Beijing 100029, China.
Yangang WangSchool of Graduate, Hebei University of Chinese Medicine, Shijiazhuang 050091, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Current targeted therapies for gastric cancer have limited efficacy, and recently discovered markers have not significantly improved survival rates in patients with gastric cancer. Therefore, it is imperative to identify more specific genes associated with the occurrence and progression of gastric cancer to achieve prevention and treatment. The aim of this study is to discover high-risk genes for gastric cancer by integrating single-cell transcriptomics and Mendelian randomization (MR) analysis. Methods: This study integrates gastric cancer genome-wide association study (GWAS) data, single-cell transcriptomics (sc-RNA-seq), and expression quantitative trait loci (eQTL) data for analysis, and employs two-sample MR to elucidate the causal relationships between genes and gastric cancer, thereby identifying high-risk genes for gastric cancer. Subsequently, in vitro cellular experiments are conducted to validate the transcriptional expression levels of these genes. Results: After quality control of the sc-RNA-seq data, we identified 2463 markers for gastric cancer cell subtypes. Subsequently, we utilized eQTL data and GWAS data for gastric cancer to perform MR analysis, yielding 149 genes with a causal relationship with gastric cancer. By applying log2FC filtering, we ultimately identified 5 high-risk gastric cancer genes: SORBS3, RMND5A, FBXO6, LPGAT1, and EPHB4. Finally, in vitro validation confirmed the differential expression of these 5 high-risk genes between normal gastric epithelial cell lines and gastric cancer cell lines. Conclusions: Our study reveals previously unattended high-risk gastric cancer genes, potentially offering new directions and evidence for the molecular diagnosis and treatment of gastric cancer.

Indexed as

Gastric cancerMendelian randomizationSc-RNA-seq

Identifiers

PMID41050213
PMCPMC12494826

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