Evidence map›Paper›PMID 41024045›Full record

ArticleBreast cancer research : BCR2025

Hsa-miR-155-5p expression in primary breast tissue may have the potential for prediction of breast cancer brain recurrence: results from the multi-institutional exploratory cohort study.

Yoichi Koyama, Masako Muguruma, Yoshiya Horimoto, Kazutaka Narui, Akimitsu Yamada, Kimito Yamada, Shinya Yamamoto, Shunichiro Orihara, Hiroshi Kaise, Akiko Kogure and 3 more

Abstract readMulticenter Study
In one paragraph

Article in Breast cancer research : BCR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Yoichi KoyamaDepartment of Breast Surgical Oncology, Tokyo Medical University Hospital, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan. peach@tokyo-med.ac.jp.ORCID http://orcid.org/0000-0001-7435-1346
Masako MugurumaDepartment of Breast Surgical Oncology, Tokyo Medical University Hospital, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.ORCID https://orcid.org/0009-0006-2269-0411
Yoshiya HorimotoDepartment of Breast Surgical Oncology, Tokyo Medical University Hospital, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.ORCID https://orcid.org/0000-0001-8935-0768
Kazutaka NaruiDepartment of Breast and Thyroid Surgery, Yokohama City University Medical Center, 4-57 Urafune-cho, Naka-ku, Yokohama city, 232-0024, Kanagawa, Japan.ORCID https://orcid.org/0000-0002-0135-5001
Akimitsu YamadaDepartment of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama city, 236-0004, Kanagawa, Japan.ORCID https://orcid.org/0000-0003-3006-0648
Kimito YamadaDepartment of Breast Surgical Oncology, Tokyo Medical University Hachioji Medical Center, 1163 Tatemachi, Hachioji city, Tokyo, 193-0998, Japan.ORCID https://orcid.org/0000-0002-5443-7078
Shinya YamamotoDepartment of Breast Surgery, Yokohama Rosai Hospital, 3211 Kozukue-cho, Kohoku-ku, Yokohama City, 222-0036, Kanagawa, Japan.ORCID https://orcid.org/0000-0002-8083-5387
Shunichiro OriharaDepartment of Health Data Science, Tokyo Medical University, 6-1-1 Shinjuku, Shinjuku- ku, Tokyo, 160-8402, Japan.ORCID https://orcid.org/0000-0003-0168-1250
Hiroshi KaiseDepartment of Breast Surgical Oncology, Tokyo Medical University Hospital, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.ORCID https://orcid.org/0000-0002-6638-783X
Akiko KogureDepartment of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.
Yusuke YoshiokaDepartment of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan.
Takahiro OchiyaDepartment of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan. tochiya@tokyo-med.ac.jp.ORCID https://orcid.org/0000-0002-0776-9918
Takashi IshikawaDepartment of Breast Surgical Oncology, Tokyo Medical University Hospital, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo, 160-0023, Japan. tishik55@gmail.com.ORCID https://orcid.org/0000-0003-3450-4533

Funding

Chugai Pharmaceutical CGPS20230417008Kyowa Kirin KKCS20230412004Nippon Kayaku NKCS20230403003Taiho Pharmaceutical AS2023A000703337
6 · The paper itself

Abstract

backgroundDespite the known incidence of brain metastases in breast cancer, no useful biomarker has been clinically established for breast cancer brain metastasis (BCBM). In the present study, we aimed to examine the expression of microRNAs (miRNAs) related to BCBM in formalin-fixed paraffin-embedded (FFPE) tissues to identify their usefulness as predictive biomarkers of breast cancer brain recurrence (BCBR).

methodsPairs of primary breast and metastatic site tissue samples were collected from 38 patients who experienced the first recurrence of metastasis to a single distant organ (brain/lungs/liver/bones = 11/12/9/6 patients) between January 2007 and December 2021 at five institutions in Japan. We evaluated the expression of 15 miRNAs in FFPE specimens of untreated breast and metastatic sites from the same patient using quantitative polymerase chain reaction.

resultsAnalysis of the selected 15 miRNAs revealed that hsa-miR-155-5p exhibited significant BCBR-specific overexpression in untreated primary breast tissues (p < 0.001). Two other miRNAs, hsa-miR-150-5p and hsa-miR-20b-5p, exhibited moderate (ρ = 0.587) and weak (ρ = 0.350) positive correlations with hsa-miR-155-5p, respectively. The BCBR prediction model demonstrated a high discrimination ability for hsa-miR-155-5p (AUC = 0.960). The localization of hsa-miR-155-5p in primary breast cancer tissue by in situ hybridization confirmed that hsa-miR-155-5p was uniformly stained in the breast cancer cells.

conclusionsHsa-miR-155-5p expression in untreated primary breast tissue may be a valuable biomarker for predicting BCBR. A personalized escalation strategy is expected to be helpful in conquering brain metastases.

Indexed as

Biomarkers, TumorBrain NeoplasmsBreast NeoplasmsMicroRNAsNeoplasm Recurrence, LocalAdultAgedCohort StudiesFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedPrognosisBiomarkers, TumorMicroRNAsMIRN155 microRNA, humanBrain recurrenceBreast cancerFormalin-fixed paraffin-embedded tissueHsa-miR-155-5pMicroRNAPolymerase chain reaction

Identifiers

PMID41024045
PMCPMC12482611

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Registered trials

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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.