Evidence map›Paper›PMID 38892411›Full record

ReviewInternational journal of molecular sciences2024

Guardians and Mediators of Metastasis: Exploring T Lymphocytes, Myeloid-Derived Suppressor Cells, and Tumor-Associated Macrophages in the Breast Cancer Microenvironment.

Maria Rosaria Ruocco, Armando Gisonna, Vittoria Acampora, Anna D'Agostino, Barbara Carrese, Jessie Santoro, Alessandro Venuta, Rosarita Nasso, Nicola Rocco, Daniela Russo and 6 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
–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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

16 authors.

Maria Rosaria RuoccoDepartment of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 80131 Naples, Italy.
Armando GisonnaDepartment of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 80131 Naples, Italy.
Vittoria AcamporaDepartment of Public Health, University of Naples Federico II, 80131 Naples, Italy.
Anna D'AgostinoIRCCS SYNLAB SDN, Via Emanuele Gianturco 113, 80143 Naples, Italy.ORCID 0000-0002-1394-4786
Barbara CarreseIRCCS SYNLAB SDN, Via Emanuele Gianturco 113, 80143 Naples, Italy.
Jessie SantoroIRCCS SYNLAB SDN, Via Emanuele Gianturco 113, 80143 Naples, Italy.
Alessandro VenutaDepartment of Public Health, University of Naples Federico II, 80131 Naples, Italy.
Rosarita NassoDepartment of Movement Sciences and Wellness, University of Naples "Parthenope", 80133 Naples, Italy.
Nicola RoccoDepartment of Advanced Biomedical Science, University of Naples Federico II, 80131 Naples, Italy.
Daniela RussoDepartment of Advanced Biomedical Science, University of Naples Federico II, 80131 Naples, Italy.
Annachiara CavalierePlastic Surgery Unit, University of Naples Federico II, 80131 Naples, Italy.ORCID 0000-0002-1776-2875
Giovanna Giuseppina AltobelliDepartment of Advanced Biomedical Science, University of Naples Federico II, 80131 Naples, Italy.
Stefania MasoneDepartment of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Naples, Italy.
Angelica AvaglianoDepartment of Public Health, University of Naples Federico II, 80131 Naples, Italy.
Alessandro ArcucciDepartment of Public Health, University of Naples Federico II, 80131 Naples, Italy.
Giuseppe FiumeDepartment of Experimental and Clinical Medicine, University of Catanzaro "Magna Graecia", 88100 Catanzaro, Italy.ORCID 0000-0002-5414-6190

Funding

Regione Campania "SATIN" grant 2018-2020
6 · The paper itself

Abstract

Breast cancers (BCs) are solid tumors composed of heterogeneous tissues consisting of cancer cells and an ever-changing tumor microenvironment (TME). The TME includes, among other non-cancer cell types, immune cells influencing the immune context of cancer tissues. In particular, the cross talk of immune cells and their interactions with cancer cells dramatically influence BC dissemination, immunoediting, and the outcomes of cancer therapies. Tumor-infiltrating lymphocytes (TILs), tumor-associated macrophages (TAMs), and myeloid-derived suppressor cells (MDSCs) represent prominent immune cell populations of breast TMEs, and they have important roles in cancer immunoescape and dissemination. Therefore, in this article we review the features of TILs, TAMs, and MDSCs in BCs. Moreover, we highlight the mechanisms by which these immune cells remodel the immune TME and lead to breast cancer metastasis.

Indexed as

Breast NeoplasmsLymphocytes, Tumor-InfiltratingMyeloid-Derived Suppressor CellsNeoplasm MetastasisTumor-Associated MacrophagesTumor MicroenvironmentAnimalsFemaleHumansT-Lymphocytesbreast cancersmetastasismyeloid-derived suppressor cellstumor-associated macrophagestumor-infiltrating lymphocytestumor microenvironment

Identifiers

PMID38892411
PMCPMC11172575

What OpenQuestion holds

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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 OpenQuestion graph.