Evidence map›Paper›PMID 41332104›Full record

ArticleCancer research communications2025

Association of Neuronal Autoantibodies with Overall Survival in Patients with Gastric Cancer.

Guanghui Liu, Xin Tan, Kaibiao Xu, Jingsi Liu, Qianhui Zheng, Xiaoyun Huang, Suyue Pan, Guoxin Li, Yafang Hu, Hao Liu

Abstract read
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Article in Cancer research communications, 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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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Guanghui Liu *Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0009-0003-0928-1312
Xin Tan *Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0009-0001-6657-5208
Kaibiao Xu *Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0009-0009-5828-8004
Jingsi LiuDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0009-0009-9885-2204
Qianhui ZhengDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0009-0003-9252-330X
Xiaoyun HuangJC School of Public Health and Primary Care, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID 0000-0002-3389-9759
Suyue PanDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0003-2744-1984
Guoxin LiDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0003-2773-7048
Yafang HuDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0001-6162-400X
Hao LiuDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0003-1227-2954

Funding

Nanfang Hospital 2021CR003National Natural Science Foundation of China (NSFC) #82272991Special Project for Research and Development in Key areas of Guangdong Province () 2023B1111050009
6 · The paper itself

Abstract

Neuronal autoantibodies have been identified in immune-mediated encephalitis, most of which are related to paraneoplastic neurologic syndromes (PNS). We detected neuronal autoantibodies in patients with gastric cancer without PNS and illustrated their correlation with clinical prognosis. All serum samples were tested by the mouse brain tissue-based assay (TBA) using immunofluorescence for screening neuronal autoantibodies. Known PNS-related neuronal autoantibodies were detected by cell-based assay. A single-center cohort has been started in Nanfang Hospital. The T-cell status of the tumor microenvironment was assessed. Single-cell sequencing was performed with limited tumor samples. Patients were grouped into TBA-positive (n = 144) and TBA-negative (n = 179) groups by the TBA status. Further screening of TBA+ specimens using the cell-based assay method revealed known PNS-related autoantibodies in 13.2% (19/144) of cases. Additionally, TBA-positive patients with gastric cancer exhibited lower CD8+ T-cell infiltration in the tumor tissue. The survival analysis show that neuronal autoantibodies in patients (TBA-positive) were associated with shorter overall survival (OS; P = 0.014). In the multivariate survival analysis, TBA positivity was still associated with shortened OS after adjusting the major covariates (HR = 2.28; 95% confidence interval, 1.31-3.97; P = 0.004). Meanwhile, single-cell sequencing indicates that cell junction assembly and synapse organization may play important roles in biological process. In this cohort study, neuronal autoantibodies were highly prevalent among patients with gastric cancer and were associated with shortened OS and features of immunosuppression within the tumor microenvironment, suggesting a candidate for exploring therapeutic relevance, with further mechanistic studies needed for validation. SIGNIFICANCE: Neuronal autoantibodies are prevalent in patients with gastric cancer, and patients without neurologic symptoms are linked to shorter survival and immunosuppression. These results provide a new direction for prognostic biomarkers and targeted therapy exploration.

Indexed as

AutoantibodiesNeuronsParaneoplastic Syndromes, Nervous SystemStomach NeoplasmsAdultAgedAnimalsCD8-Positive T-LymphocytesFemaleHumansMaleMiceMiddle AgedPrognosisSingle-Cell AnalysisTumor MicroenvironmentAutoantibodies

Identifiers

PMID41332104
PMCPMC12673196

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