Evidence map›Paper›PMID 40817076›Full record

ArticleCell death discovery2025

Lead bioaccumulation in human breast cancer tissue is associated with DNA instability and cell death resistance.

Manuel Scimeca, Erica Giacobbi, Rita Bonfiglio, Renata Sisto, Stefano Casciardi, Francesca Servadei, Daniel R S Middleton, Julia Bischof, Maria Paola Scioli, Giorgio Modesti and 3 more

Abstract read
In one paragraph

Article in Cell death discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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.

Manuel Scimeca *Department of Experimental Medicine, TOR, University of Rome "Tor Vergata", Rome, Italy. manuel.scimeca@uniroma2.it.
Erica Giacobbi *Department of Experimental Medicine, TOR, University of Rome "Tor Vergata", Rome, Italy.
Rita Bonfiglio *Department of Experimental Medicine, TOR, University of Rome "Tor Vergata", Rome, Italy.
Renata SistoDepartment of Occupational and Environmental Medicine, Epidemiology and Hygiene, INAIL Research, Monte Porzio Catone, Rome, Italy.
Stefano CasciardiDepartment of Occupational and Environmental Medicine, Epidemiology and Hygiene, INAIL Research, Monte Porzio Catone, Rome, Italy.
Francesca ServadeiDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", Rome, Italy.ORCID http://orcid.org/0000-0003-2619-9153
Daniel R S MiddletonCancer Epidemiology Research Group, Centre for Public Health, Queen's University Belfast, Belfast, UK.
Julia BischofIndivumed GmbH, Falkenried, Hamburg, Germany.
Maria Paola ScioliDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", Rome, Italy.
Giorgio ModestiIndivumed GmbH, Falkenried, Hamburg, Germany.
Eleonora CandiDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", Rome, Italy.ORCID http://orcid.org/0000-0001-8332-4825
Gerry MelinoDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", Rome, Italy.
Alessandro MaurielloDepartment of Experimental Medicine, TOR, University of Rome "Tor Vergata", Rome, Italy.ORCID http://orcid.org/0000-0002-7351-5676

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lead (Pb) is increasingly recognized for its potential to alter cellular processes and contribute to cancer development. Although Pb is classified as a probable carcinogen by the IARC, the clinical evidence for its role in breast cancer is inconsistent and limited to epidemiological studies yet. The aim of this study was to investigate the Pb bioaccumulation in human breast cancer tissues by correlating its concentration with specific cancer factors related to carcinogenesis. Biopsy samples from 26 breast cancer patients were collected for molecular investigations (DNA and RNA sequencing), histological analysis, and the assessment of Pb concentration by ICP-MS. Data reported here revealed Pb bioaccumulation in all breast cancer samples, with a significant positive correlation between Pb levels and both Tumoral Mutational Burden and Microsatellite Instability, suggesting an association of Pb with genomic instability in human breast cancer samples. Additionally, Pb was associated with increased expression of cell death-related molecules such as BCL2 and p53. This association allows us to hypothesize a potential involvement of Pb in affecting cell death resistance. Interestingly, Pb concentration showed no correlation to other established prognostic and predictive biomarkers of breast cancer, such as PAM50. Thus, Pb concentration may represent a new independent risk factor for breast cancer development. This study provides new insights into the role of Pb bioaccumulation in breast cancer and suggests that environmental exposure to Pb may contribute to more aggressive tumor behavior through mechanisms involving genomic instability and resistance to apoptosis.

Identifiers

PMID40817076
PMCPMC12356885

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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.