Evidence map›Paper›PMID 40764893›Full record

ArticleDiscover oncology2025

Causal relationships between immune cell traits and HER2 subtypes in breast cancer: a Mendelian randomization study.

Fenfen Gu, Chuling Hu, Chao Li

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Fenfen Gu *Department of Clinical Pharmacy, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, No. 1665 Kongjiang Road, Yangpu District, Shanghai, 200092, PR China.
Chuling Hu *Department of Clinical Pharmacy, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, No. 1665 Kongjiang Road, Yangpu District, Shanghai, 200092, PR China.
Chao LiDepartment of Clinical Pharmacy, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, No. 1665 Kongjiang Road, Yangpu District, Shanghai, 200092, PR China. lichao@xinhuamed.com.cn.

Funding

Fundamental Research Funds for the Central Universities 24X010301395
6 · The paper itself

Abstract

backgroundBreast cancer can be classified based on HER2 status into HER2-positive (HER2+) and HER2-negative (HER2-) subtypes, which differ significantly in pathogenesis, prognosis, and treatment response. Immune cells are critical components of the tumor microenvironment, influencing breast cancer progression. However, their specific roles in HER2 + and HER2- breast cancer subtypes are not yet fully understood.

methodsThis study applied Mendelian randomization (MR) analysis to investigate causal relationships between 731 immune cell phenotypes and breast cancer with different HER2 statuses. Genetic data were obtained from the Finngen and OPENGWAS databases. Inverse variance weighted (IVW) analysis and sensitivity tests were used to ensure the robustness of results.

resultsOur analysis revealed significant associations between specific immune cell traits and breast cancer subtypes. For instance, B cell traits such as "Sw mem %B cell" and "IgD- CD38- %B cell" were positively correlated with the development of HER2 + breast cancer. Conversely, traits associated with T cell maturation and myeloid cells demonstrated a negative correlation with HER2 + breast cancer. Regulatory T cell traits were more strongly linked to HER2- breast cancer.

conclusionsDistinct immune cell profiles are associated with HER2 + and HER2- breast cancers. These findings provide insights into the immunological differences between subtypes and suggest potential targets for personalized immunotherapy strategies. Further research is required to clarify underlying mechanisms.

Indexed as

Breast cancerHER2Immune cellsMendelian randomization

Identifiers

PMID40764893
PMCPMC12325163

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