Evidence map›Paper›PMID 37118737›Full record

ArticleJournal of translational medicine2023

The intratumour microbiota and neutrophilic inflammation in squamous cell vulvar carcinoma microenvironment.

Natalia Rustetska, Magdalena Szczepaniak, Krzysztof Goryca, Elwira Bakuła-Zalewska, Małgorzata Figat, Artur Kowalik, Stanisław Góźdź, Magdalena Kowalewska

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 16 citations in OpenAlex.

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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

8 authors at 4 institutions in 2 countries.

Natalia RustetskaDepartment of Molecular and Translational Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Warsaw, Poland.
Magdalena SzczepaniakDepartment of Molecular Diagnostics, Holycross Cancer Centre, 25-734, Kielce, Poland.
Krzysztof GorycaGenomics Core Facility, Centre of New Technologies, University of Warsaw, 02-097, Warsaw, Poland.
Elwira Bakuła-ZalewskaDepartment of Pathology, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Warsaw, Poland.
Małgorzata FigatDepartment of Gynecologic Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, 02-097, Warsaw, Poland.
Artur KowalikDepartment of Molecular Diagnostics, Holycross Cancer Centre, 25-734, Kielce, Poland.
Stanisław GóźdźDepartment of Clinical Oncology, Holycross Cancer Centre, 25-734, Kielce, Poland.
Magdalena KowalewskaDepartment of Molecular and Translational Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Warsaw, Poland. magdalena.kowalewska@pib-nio.pl.ORCID 0000-0002-3413-9612
The Maria Sklodowska-Curie National Research Institute of Oncology · PLJan Kochanowski University · PLNational Institute of Oncology · HUUniversity of Warsaw · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA causal link between microbiota composition (dysbiosis) and oncogenesis has been demonstrated for several types of cancer. Neutrophils play a role in both immune protection against bacterial threats and carcinogenesis. This study aimed to characterise intratumoral bacteria in vulvar squamous cell carcinoma (VSCC) and their putative effect on neutrophil recruitment and cancer progression.

methodsClinical material was obtained from 89 patients with VSCC. Next-generation sequencing (NGS) of 16S rRNA and quantitative polymerase chain reaction (qPCR) were used to detect bacterial species in VSCC. To verify neutrophil activation, CD66b expression in tumour specimens was analysed by immunohistochemistry (IHC). Subsequently, IHC was applied to detect the main neutrophil serine proteases (NSPs), cathepsin G (CTSG), neutrophil elastase (ELANE), and proteinase 3 (PRTN3) in VSCC.

resultsFusobacterium nucleatum and Pseudomonas aeruginosa were identified as tumour-promoting bacteria, and their presence was found to be associated with a shorter time to progression in VSCC patients. Furthermore, high abundance of CD66b, the neutrophil activation marker, in VSCC samples, was found to relate to poor survival of patients with VSCC. The selected NSPs were shown to be expressed in vulvar tumours, also within microabscess. The increased numbers of microabscesess were correlated with poor survival in VSCC patients.

conclusionsOur results show that neutrophilic inflammation seem to be permissive for tumour-promoting bacteria growth in VSCC. The findings provide new therapeutic opportunities, such as based on shifting the balance of neutrophil populations to those with antitumorigenic activity and on targeting NSPs produced by activated neutrophils at the inflammation sites.

Indexed as

Carcinoma, Squamous CellVulvar NeoplasmsEpithelial CellsFemaleHumansInflammationRNA, Ribosomal, 16STumor MicroenvironmentRNA, Ribosomal, 16SFusobacterium nucleatumMicroabscessMicrobiotaNeutrophil serine proteasePseudomonas aeruginosaVulvar carcinoma

Identifiers

PMID37118737
PMCPMC10141905
OpenAlexW4367318411

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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.