Evidence map›Paper›PMID 40442728›Full record

ArticleBreast cancer research : BCR2025

Identification of vitronectin as a potential non-invasive biomarker of metastatic breast cancer using a label-free LC-MS/MS approach.

Roopali Roy, Elisa M Schunkert, Petra Olivova, Martin Gilar, Scott Geromanos, Guo-Zhong Li, John Gebler, Adelle Dagher, Andrew El-Hayek, Rama Aldakhlallah and 5 more

Abstract read
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

15 authors.

Roopali Roy *Vascular Biology Program, Karp Family Research Building, Harvard Medical School, Boston Children's Hospital, 12.214, 300 Longwood Avenue, Boston, MA, 02115, USA. roopali.roy@childrens.harvard.edu.
Elisa M Schunkert *Vascular Biology Program, Karp Family Research Building, Harvard Medical School, Boston Children's Hospital, 12.214, 300 Longwood Avenue, Boston, MA, 02115, USA.
Petra OlivovaWaters Corporation, Milford, MA, USA.
Martin GilarWaters Corporation, Milford, MA, USA.
Scott GeromanosWaters Corporation, Milford, MA, USA.
Guo-Zhong LiWaters Corporation, Milford, MA, USA.
John GeblerWaters Corporation, Milford, MA, USA.
Adelle DagherVascular Biology Program, Karp Family Research Building, Harvard Medical School, Boston Children's Hospital, 12.214, 300 Longwood Avenue, Boston, MA, 02115, USA.
Andrew El-HayekVascular Biology Program, Karp Family Research Building, Harvard Medical School, Boston Children's Hospital, 12.214, 300 Longwood Avenue, Boston, MA, 02115, USA.
Rama AldakhlallahVascular Biology Program, Karp Family Research Building, Harvard Medical School, Boston Children's Hospital, 12.214, 300 Longwood Avenue, Boston, MA, 02115, USA.
Steven J StaffaDepartment of Surgery, Harvard Medical School and Boston Children's Hospital, Boston, MA, USA.
David ZurakowskiDepartment of Surgery, Harvard Medical School and Boston Children's Hospital, Boston, MA, USA.
Margaret LotzHoffman Breast Center, Mount Auburn Hospital, Cambridge, MA, USA.
Susan PoriesHoffman Breast Center, Mount Auburn Hospital, Cambridge, MA, USA.
Marsha A MosesVascular Biology Program, Karp Family Research Building, Harvard Medical School, Boston Children's Hospital, 12.214, 300 Longwood Avenue, Boston, MA, 02115, USA. marsha.moses@childrens.harvard.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer (BC) is a complex heterogenous disease that is a leading cause of death in women. For patients with early stage disease following primary BC therapy, approximately 30% will develop metastatic BC (MBC). The median survival of MBC patients is ~ 2-3 yr. While the early detection and monitoring of BC progression have improved prognosis and reduced BC-related mortality, there is a lack of long-term surveillance strategies for monitoring patients for recurrence of MBC. The aim of our study was to identify non-invasive urinary biomarkers for detection and monitoring of MBC.

methodsWe have conducted a comparative label-free LC-MS/MS analysis of the urinary proteome of patients with MBC and healthy age-matched, sex-matched controls (HC). A hybrid quadrupole time of flight (Q-Tof™) mass spectrometer was used for urine analysis via liquid chromatography (LC) with tandem mass spectrometry (MS/MS). Retrospective analysis of urine samples from MBC and locally invasive breast cancer (IBC) patients as well as HC was conducted. Diagnostic accuracies of candidate markers were validated using independent training and validation sets according to the REMARK criteria.

resultsUsing this approach, we have identified 212 urinary proteins of which 83 and 25 were unique to the MBC and HC groups, respectively. Upregulated proteins in the MBC cohort were associated with angiogenesis, Ca

conclusionsOur findings suggest that uVTN is a promising and non-invasive biomarker for the diagnosis and monitoring of MBC. While future validation in larger cohorts should be done, these results identify a novel urinary protein that represents the first non-invasive diagnostic test for monitoring BC progression and recurrence.

Indexed as

Biomarkers, TumorBreast NeoplasmsVitronectinAdultAgedCase-Control StudiesChromatography, LiquidFemaleHumansLiquid Chromatography-Mass SpectrometryMiddle AgedNeoplasm MetastasisPrognosisProteomicsRetrospective StudiesTandem Mass SpectrometryBiomarkers, TumorVitronectinLiquid chromatography with tandem mass spectrometry (LC–MS/MS)Metastatic breast cancerREMARKSurveillanceUrinary biomarkersVitronectin

Identifiers

PMID40442728
PMCPMC12123798

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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.