Evidence map›Paper›PMID 39501160›Full record

ArticleMolecular medicine (Cambridge, Mass.)2024

Increased levels of versican and insulin-like growth factor 1 in peritumoral mammary adipose tissue are related to aggressiveness in estrogen receptor-positive breast cancer.

Paola Mirra, Alessia Parascandolo, Graziella Marino, Federica D'Alterio, Lorenza Zinna, Antonella Desiderio, Giuseppe Patitucci, Giulia Anna Carmen Vita, Valentina Condelli, Sabino Russi and 5 more

Abstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. The role of OCT4 and CD44 in lower lip carcinogenesis.Oral and maxillofacial surgery · 2025
    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.

Paola Mirra *URT "Genomic of Diabetes", Institute for Experimental Endocrinology and Oncology "G. Salvatore", National Research Council (IEOS-CNR), Via Pansini 5, 80131, Naples, Italy.
Alessia Parascandolo *Department of Translational Medicine, University of Naples "Federico II", Via Pansini 5, 80131, Naples, Italy.
Graziella MarinoDepartment of Breast Surgery, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) CROB Centro di Riferimento Oncologico della Basilicata, Rionero in Vulture, Italy.
Federica D'AlterioDepartment of Translational Medicine, University of Naples "Federico II", Via Pansini 5, 80131, Naples, Italy.
Lorenza ZinnaDepartment of Translational Medicine, University of Naples "Federico II", Via Pansini 5, 80131, Naples, Italy.
Antonella DesiderioDepartment of Translational Medicine, University of Naples "Federico II", Via Pansini 5, 80131, Naples, Italy.
Giuseppe PatitucciDepartment of Anatomical Pathology, Centro di Riferimento oncologico della Basilicata (IRCCS CROB), Rionero in Vulture, Italy.
Giulia Anna Carmen VitaDepartment of Anatomical Pathology, Centro di Riferimento oncologico della Basilicata (IRCCS CROB), Rionero in Vulture, Italy.
Valentina CondelliLaboratory of Preclinical and Translational Research, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) CROB Centro di Riferimento Oncologico della Basilicata, Rionero in Vulture, Italy.
Sabino RussiLaboratory of Preclinical and Translational Research, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) CROB Centro di Riferimento Oncologico della Basilicata, Rionero in Vulture, Italy.
Francesco D'AndreaDepartment of Public Health, University of Naples "Federico II", Via Pansini 5, 80131, Naples, Italy.
Francesco BeguinotURT "Genomic of Diabetes", Institute for Experimental Endocrinology and Oncology "G. Salvatore", National Research Council (IEOS-CNR), Via Pansini 5, 80131, Naples, Italy.
Claudia MieleURT "Genomic of Diabetes", Institute for Experimental Endocrinology and Oncology "G. Salvatore", National Research Council (IEOS-CNR), Via Pansini 5, 80131, Naples, Italy.
Pietro FormisanoURT "Genomic of Diabetes", Institute for Experimental Endocrinology and Oncology "G. Salvatore", National Research Council (IEOS-CNR), Via Pansini 5, 80131, Naples, Italy. fpietro@unina.it.ORCID 0000-0001-7020-6870
Vittoria D'EspositoURT "Genomic of Diabetes", Institute for Experimental Endocrinology and Oncology "G. Salvatore", National Research Council (IEOS-CNR), Via Pansini 5, 80131, Naples, Italy.

Funding

Finanziato dall'Unione europea - Next Generation EU" -NATIONAL RECOVERY AND RESILIENCE PLAN (NRRP) - MISSION 4, COMPONENT 2 INVESTMENT 1.1 - "Fund for the National Research Program and for Projects of National Interest (NRP) Prot. P2022KWK8F - CUP B53D23027590001Finanziato dall'Unione europea - Next Generation EU" -NATIONAL RECOVERY AND RESILIENCE PLAN (NRRP) - MISSION 4, COMPONENT 2 INVESTMENT 1.1 - "Fund for the National Research Program and for Projects of National Interest (NRP) Prot. P2022LPJM4-CUP E53D23019900001Fondazione AIRC per la ricerca sul cancro ETS IG2023-29378Regione Campania POR FESR 2014-2020 Objective 1.2-Coepica project
6 · The paper itself

Abstract

The adipose tissue (AT) surrounding breast cancer (BC) plays a pivotal role in cancer progression and represents an optimal source for new biomarker discovery. The aim of this work was to investigate whether specific AT factors may have prognostic value in estrogen receptor-positive (ER+) BC. Proteoglycan Versican (VCAN), Insulin-like Growth Factor 1 (IGF1), Reticulon 4B (RTN4), chemokines CCL5 (also known as RANTES) and interleukin 8 (IL-8) are expressed in AT and may play important roles in BC progression. Peritumoral AT and tumoral biopsies were obtained from patients with ER+ BC (N = 23). AT specimens were collected also from healthy women (N = 17; CTRL-AT). The analysis of gene expression by qPCR revealed significantly higher mRNA levels of VCAN, IGF1, RTN4, and CCL5 in BC-AT compared to the CTRL-AT, and no difference in IL-8 mRNA levels. VCAN positively correlated with patient Body Mass Index (BMI) in BC-AT, while not in CTRL-AT. Moreover, VCAN and IGF1 positively correlated with RTN4 and negatively with CCL5. Interestingly, VCAN correlated with tumoral Ki67, while IGF1 with tumoral OCT4 that, in turn, correlated with tumoral Ki67 and patient BMI. Thus, peritumoral AT content of VCAN, and IGF1 are related to BC proliferation and aggressiveness.

Indexed as

Adipose TissueBreast NeoplasmsInsulin-Like Growth Factor IReceptors, EstrogenVersicansAdultAgedBiomarkers, TumorChemokine CCL5FemaleGene Expression Regulation, NeoplasticHumansInsulin-Like PeptidesMiddle AgedPrognosisBiomarkers, TumorChemokine CCL5IGF1 protein, humanInsulin-Like Growth Factor IInsulin-Like PeptidesReceptors, EstrogenVCAN protein, humanVersicansBiomarkersBMIBreast cancerIGF-1Mammary adipose tissueVersican

Identifiers

PMID39501160
PMCPMC11539550

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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.