Evidence map›Paper›PMID 39009451›Full record

ArticleJournal for immunotherapy of cancer2024

Assessing the implications of sentinel lymph node removal in cervical cancer: an immunogenetic perspective - a SENTICOL ancillary study.

Gaurav Thareja, Anna Salvioni, Françoise Lauzeral-Vizcaino, Najeeb Halabi, Eliane Mery-Lamarche, Noemie Thebault, Clara-Maria Scarlata, Marie Michelas, Anne-Sophie Navarro, Gwenaël Ferron and 6 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 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. 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

16 authors.

Gaurav TharejaWeill Cornell Medicine, Doha, Qatar.ORCID http://orcid.org/0000-0003-2277-6400
Anna SalvioniCentre de recherche en cancerologie de Toulouse, Toulouse, France.
Françoise Lauzeral-VizcainoCentre de Recherches en Cancérologie de Toulouse INSERM UMR1037, Toulouse, France.
Najeeb HalabiWeill Cornell Medicine, Doha, Qatar.
Eliane Mery-LamarchePathology Department, Oncopole Claudius Regaud, Institut Universitaire du Cancer Toulouse Oncopole, Toulouse, France.
Noemie ThebaultCentre de Recherches en Cancérologie de Toulouse INSERM UMR1037, Toulouse, France.
Clara-Maria ScarlataCentre de Recherches en Cancérologie de Toulouse INSERM UMR1037, Toulouse, France.
Marie MichelasCentre de Recherches en Cancérologie de Toulouse INSERM UMR1037, Toulouse, France.
Anne-Sophie NavarroSurgical Oncology Department, Oncopole Claudius Regaud, Institut Universitaire du Cancer Toulouse Oncopole, Toulouse, France.
Gwenaël FerronCentre de Recherches en Cancérologie de Toulouse INSERM UMR1037, Toulouse, France.
Fabrice LecuruGynecologic Oncology Department, Institut Curie, Paris, France.
Patrice MathevetGynecology Department, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
Jonathan KhalifaCentre de Recherches en Cancérologie de Toulouse INSERM UMR1037, Toulouse, France.
Maha AyyoubCentre de Recherches en Cancérologie de Toulouse INSERM UMR1037, Toulouse, France.
Arash RafiiScieNFT, Paris, France.
Alejandra MartinezCentre de Recherches en Cancérologie de Toulouse INSERM UMR1037, Toulouse, France martinez.alejandra@iuct-oncopole.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCervical cancer's lymphatic spread primarily begins from the sentinel lymph nodes (SLNs), underlining their pivotal role in disease metastasis. However, these nodes' immune gene expression profiles and immunoregulation mechanisms have yet to be explored.

methodsOur study aimed to elucidate the immune cell populations and their roles in the immune gene expression profile of negative SLNs compared with positive SLNs and non-SLNs using Nanostring RNA seq analysis. We performed a principal component analysis on the log2 normalized expression of 685 endogenous genes in the nCounter PanCancer Immune Profiling Panel, followed by an assessment of the differential expression of genes and immune cell type abundance.

resultsWe found significant variations in gene expression among the groups, with negative SLNs displaying overexpression of genes related to tumor-infiltrating immune cells, specifically innate cell populations. They also demonstrated the upregulation of genes involved in antigen presentation and T-cell priming. In contrast, positive SLNs were enriched in regulatory networks, suggesting their potential role in immune evasion. A comparison of negative SLNs and non-SLNs revealed increased innate and adaptive immune cell types, underscoring the ongoing T cell response to tumor antigens.

conclusionOur findings underscore a specific immunogenetic phenotype profile in negative SLNs, emphasizing their crucial role in the initial anticancer response, immunosurveillance, and the propagation of immune tolerance from the primary cervical tumor. These results highlight the potential of SLNs as a novel target for immunotherapy strategies and underscore the importance of new imaging methods for accurately identifying SLN status without removal. Future investigations are needed to understand further the immunological interplay within SLNs and their influence on cervical cancer progression.

Indexed as

Sentinel Lymph NodeUterine Cervical NeoplasmsFemaleHumansImmunogeneticsLymphatic MetastasisMiddle AgedSentinel Lymph Node BiopsyImmune modulatory

Identifiers

PMID39009451
PMCPMC11253764

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.