Evidence map›Paper›PMID 41582199›Full record

ArticleBreast cancer research : BCR2026

High levels of circulating miR-19a-3p in patients with metastatic HER2 + breast cancer are associated with a favorable prognosis and anti-tumor immune responses.

Evan N Cohen, Hui Gao, Sanda Tin, Qiong Wu, Cristina Ivan, Naoto T Ueno, Wendy A Woodward, James M Reuben, Simone Anfossi

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 2026. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Evan N CohenDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Hui GaoDepartment of Hemopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Sanda TinDepartment of Hemopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Qiong WuDepartment of Hemopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Cristina IvanCaris Life Science, Irving, TX, 75039, USA.
Naoto T UenoDepartment of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Wendy A WoodwardDepartment of Breast Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
James M ReubenDepartment of Hemopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Simone AnfossiDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. sanfossi@mdanderson.org.ORCID http://orcid.org/0000-0001-5745-7587

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIANE BODURKA · 1985 to 2026
$290.8M
Deciphering the Mechanism of Lymphovascular Space Invasion Using a Lymphovascularized Bioengineering Breast Stromal PlatformR01CA284102 · NCI · UNIVERSITY OF TEXAS AT AUSTIN · PI Bisrat G Debeb, Marissa Nichole Rylander · 2024 to 2026
$3.3M
Human Breast Cancer Stem Cell SurrogatesR01CA138239 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CRISTOFANILLI, MASSIMO, REUBEN, JAMES MARTIN · 2008 to 2012
$2.8M
Single Cell Spatial Analysis in TissueR50CA243707 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BURKS, JARED KYLE · 2020 to 2024
$1.3M
DOD W81XWH-09-1-0031 01NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA138239NCI NIH HHS R01 CA284102NCI NIH HHS R50 CA243707NIH/NCI CA138239-02
6 · The paper itself

Abstract

backgroundTrastuzumab, combined with chemotherapy, is the current standard treatment for both metastatic and early-stage HER2-positive (HER2 +) breast cancer. One of the mechanisms of action of trastuzumab is antibody-dependent cellular cytotoxicity (ADCC), which involves engaging FcγRIIIA (CD16) on natural killer (NK) cells. A competent immune system and properly functioning NK cells are crucial for effective ADCC, as they can influence favorable clinical outcomes. Resistance to trastuzumab often develops after about one year. We previously reported that elevated levels of miR-19a-3p in the serum of patients with metastatic HER2 + breast cancer treated with trastuzumab were associated with a favorable prognosis. Here, we aim to identify the mechanism and the immune cells responsible for elevated serum levels of miR-19a-3p.

methodsPeripheral blood mononuclear cells (PBMCs) from healthy individuals were used to isolate naïve CD4 + T cells and NK cells. Naïve CD4 + T cells were polarized into CD4 + Th1 and CD4 + Th2 cells. NK cells were utilized for the ADCC assay. Levels of transcription factors, cytokines, and miR-19a-3p were measured using RT-qPCR. Surface markers and cytokines were analyzed by flow cytometry to characterize immune cell phenotypes.

resultsIn vitro NK cell-mediated ADCC resulted in increased levels of miR-19a-3p released into the supernatants after killing breast cancer cells. In vitro polarized CD4 + Th1 cells expressed and secreted higher levels of miR-19a-3p than CD4 + Th2 cells. Over a long-term in vitro culture (24 days), anti-CD3/CD28 restimulation sustained higher levels of miR-19a-3p in CD4 + Th1 cells compared to CD4 + Th2 cells and their respective supernatants. CD4 + Th1 cells developed a central memory T (T DISCUSSION: Our findings suggest that elevated levels of miR-19a-3p in the serum of patients with HER2 + metastatic breast cancer may result from effective NK cell-mediated ADCC and activation of CD4 + Th1 cells, which could be responsible for the anti-tumor immune response associated with a favorable prognosis. Blood levels of miR-19a-3p might help identify breast cancer patients who have effective trastuzumab-induced anti-tumor immune responses.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesMicroRNAsAdultAntibody-Dependent Cell CytotoxicityBiomarkers, TumorCell Line, TumorFemaleHumansKiller Cells, NaturalMiddle AgedNeoplasm MetastasisPrognosisReceptors, IgGTh1 CellsTrastuzumabBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMicroRNAsMIR19A, humanReceptors, IgGTrastuzumabADCCAnti-tumor immune responseCD4 + Th1 cellsHER2 + metastatic breast cancermiR-19a-3pNK cellsTrastuzumab

Identifiers

PMID41582199
PMCPMC12833941

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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.