Evidence map›Paper›PMID 42789703›Full record

ArticleScience advances2026

Multiplatform single-cell and spatial transcriptomics reveal sex-specific malignant states and architecture in male breast cancer.

Haoyuan Shi, Xiuli Zhang, Shouliang Cai, Baoku Xu, Haibo Wang, Jian Cui, Zitong Yang, Siyi Chen, Zhangjian Zhou, Shuqun Zhang and 5 more

Abstract read
In one paragraph

Article in Science advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Haoyuan ShiSchool of Future Medicine, Beijing University of Chinese Medicine, Beijing 100102, China.ORCID 0000-0002-6028-0185
Xiuli ZhangDepartment of Rheumatology and Clinical Immunology, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0002-5694-0101
Shouliang CaiThe Ansteel Group Hospital, Anshan 114001, Liaoning, China.ORCID 0009-0008-1566-6215
Baoku XuThe Ansteel Group Hospital, Anshan 114001, Liaoning, China.ORCID 0009-0000-3167-8613
Haibo WangThe Affiliated Hospital of Qingdao University, Qingdao 266003, China.ORCID 0000-0002-5585-704X
Jian CuiThe Affiliated Hospital of Qingdao University, Qingdao 266003, China.
Zitong YangThe First Medical Center, Chinese PLA General Hospital, Beijing 100853, China.
Siyi ChenThe First Medical Center, Chinese PLA General Hospital, Beijing 100853, China.ORCID 0009-0008-7715-926X
Zhangjian ZhouThe Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.ORCID 0000-0002-2341-6338
Shuqun ZhangThe Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.ORCID 0000-0002-6998-7849
Yifan CaiThe Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.ORCID 0000-0002-0407-1581
Yu ZhangThe Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.ORCID 0000-0002-6886-7300
Liling ZhuBreast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China.
Jiandong WangThe First Medical Center, Chinese PLA General Hospital, Beijing 100853, China.ORCID 0009-0007-5365-2087
Nianzeng XingDepartment of Urology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.ORCID 0000-0002-2696-5279

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Male breast cancer (MBC) is rare and remains largely managed using knowledge derived from female breast cancer. Here, we generated a multiplatform single-cell and spatial transcriptomic atlas integrating scRNA-seq, SeekSpace, Visium HD, Xenium In Situ, and multiplex immunohistochemistry data from male and female breast cancer cohorts, covering more than 660,000 cells. We identified male-specific tumor cells (MSTCs) that were enriched in MBC, rare in female breast cancer, and associated with poorer disease-free survival. MSTCs exhibited neural transcriptional programs, increased transcriptome-inferred copy number variation burden, and spatial coupling with fatty acid metabolism signals. MSTC-enriched regions showed reduced antigen-presentation signatures and spatial association with

Indexed as

Breast Neoplasms, MaleSingle-Cell AnalysisTranscriptomeFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMacrophagesMaleSingle-Cell Gene Expression AnalysisSpatial Transcriptomics

Identifiers

PMID42789703
PMCPMC13614381

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.