Evidence map›Paper›PMID 36346290›Full record

ArticleInternational journal of cancer2023

SPARC in cancer-associated fibroblasts is an independent poor prognostic factor in non-metastatic triple-negative breast cancer and exhibits pro-tumor activity.

Lindsay B Alcaraz, Aude Mallavialle, Caroline Mollevi, Florence Boissière-Michot, Hanane Mansouri, Joelle Simony-Lafontaine, Valérie Laurent-Matha, Thierry Chardès, William Jacot, Andrei Turtoi and 3 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.1field-weighted citation impact, top 5% of its field
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

20 citing papers in PubMed, 26 citations in OpenAlex.

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  10. Matricellular proteins: Potential biomarkers in head and neck cancer.Journal of cell communication and signaling · 2024
    Review
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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 at 2 institutions in 1 country.

Lindsay B AlcarazIRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.ORCID 0000-0003-1912-7186
Aude MallavialleIRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.ORCID 0000-0002-9380-6788
Caroline MolleviBiometry Unit, ICM, University of Montpellier, Montpellier, France.ORCID 0000-0003-4827-3684
Florence Boissière-MichotTranslational Research Unit, ICM, Montpellier, France.
Hanane MansouriIRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.
Joelle Simony-LafontaineTranslational Research Unit, ICM, Montpellier, France.
Valérie Laurent-MathaIRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.ORCID 0000-0002-3277-7397
Thierry ChardèsIRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.ORCID 0000-0002-1836-7439
William JacotIRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.ORCID 0000-0001-7834-061X
Andrei TurtoiIRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.ORCID 0000-0003-3813-6635
Pascal RogerIRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.ORCID 0000-0002-4040-5892
Séverine GuiuIRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.ORCID 0000-0002-4901-6295
Emmanuelle Liaudet-CoopmanIRCM, INSERM U1194, Univ Montpellier, ICM, Montpellier, France.ORCID 0000-0001-9313-9690
Inserm · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is the most aggressive breast cancer subtype and lacks specific targeted therapeutic agents. The current mechanistic evidence from cell-based studies suggests that the matricellular protein SPARC has a tumor-promoting role in TNBC; however, data on the clinical relevance of SPARC expression/secretion by tumor and stromal cells in TNBC are limited. Here, we analyzed by immunohistochemistry the prognostic value of tumor and stromal cell SPARC expression in 148 patients with non-metastatic TNBC and long follow-up (median: 5.4 years). We also quantified PD-L1 and PD-1 expression. We detected SPARC expression in tumor cells (42.4%), cancer-associated fibroblasts (CAFs; 88.1%), tumor-associated macrophages (77.1%), endothelial cells (75.2%) and tumor-infiltrating lymphocytes (9.8%). Recurrence-free survival was significantly lower in patients with SPARC-expressing CAFs. Multivariate analysis showed that SPARC expression in CAFs was an independent prognostic factor. We also detected tumor and stromal cell SPARC expression in TNBC cytosols, and in patient-derived xenografts and cell lines. Furthermore, we analyzed publicly available single-cell mRNA sequencing data and found that in TNBC, SPARC is expressed by different CAF subpopulations, including myofibroblasts and inflammatory fibroblasts that are involved in tumor-related processes. We then showed that fibroblast-secreted SPARC had a tumor-promoting role by inhibiting TNBC cell adhesion and stimulating their motility and invasiveness. Overall, our study demonstrates that SPARC expression in CAFs is an independent prognostic marker of poor outcome in TNBC. Patients with SPARC-expressing CAFs could be eligible for anti-SPARC targeted therapy.

Indexed as

Antineoplastic AgentsCancer-Associated FibroblastsTriple Negative Breast NeoplasmsBiomarkers, TumorEndothelial CellsHumansOsteonectinPrognosisAntineoplastic AgentsBiomarkers, TumorOsteonectinSPARC protein, humanCAFosteonectinsingle-cell mRNA sequencingSPARCTNBC

Identifiers

PMID36346290
PMCPMC10099777
OpenAlexW4308508295

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.