Evidence map›Paper›PMID 38658633›Full record

ArticleScientific reports2024

Loss of Y in regulatory T lymphocytes in the tumor micro-environment of primary colorectal cancers and liver metastases.

Magdalena Wójcik, Ulana Juhas, Elyas Mohammadi, Jonas Mattisson, Kinga Drężek-Chyła, Edyta Rychlicka-Buniowska, Bożena Bruhn-Olszewska, Hanna Davies, Katarzyna Chojnowska, Paweł Olszewski and 15 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.6field-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

17 citing papers in PubMed, 19 citations in OpenAlex.

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  15. Sex differences in disease: sex chromosome and immunity.Journal of translational medicine · 2024
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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

25 authors at 6 institutions in 3 countries.

Magdalena Wójcik *3P-Medicine Laboratory, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland.
Ulana Juhas *3P-Medicine Laboratory, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland.
Elyas Mohammadi *3P-Medicine Laboratory, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland.
Jonas MattissonDepartment of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Kinga Drężek-Chyła3P-Medicine Laboratory, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland.
Edyta Rychlicka-Buniowska3P-Medicine Laboratory, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland.
Bożena Bruhn-OlszewskaDepartment of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Hanna DaviesDepartment of Immunology, Genetics and Pathology and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Katarzyna Chojnowska3P-Medicine Laboratory, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland.
Paweł Olszewski3P-Medicine Laboratory, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland.
Michał BieńkowskiDepartment of Pathomorphology, Medical University of Gdańsk, Gdańsk, Poland.
Michał JankowskiSurgical Oncology, Ludwik Rydygier's Collegium Medicum, Bydgoszcz, Nicolaus Copernicus University, Toruń, Poland.
Olga RostkowskaDepartment of Oncological, Transplant and General Surgery, Medical University of Gdańsk, Gdańsk, Poland.
Andrzej HellmannDepartment of Oncological, Transplant and General Surgery, Medical University of Gdańsk, Gdańsk, Poland.
Rafał PęksaDepartment of Pathomorphology, Medical University of Gdańsk, Gdańsk, Poland.
Jacek KowalskiDepartment of Pathomorphology, Medical University of Gdańsk, Gdańsk, Poland.
Marek ZdrenkaDepartment of Tumor Pathology and Pathomorphology, Oncology Center - Prof. Franciszek Łukaszczyk Memorial Hospital, Bydgoszcz, Poland.
Jarek KobielaDepartment of Oncological, Transplant and General Surgery, Medical University of Gdańsk, Gdańsk, Poland.
Wojciech ZegarskiSurgical Oncology, Ludwik Rydygier's Collegium Medicum, Bydgoszcz, Nicolaus Copernicus University, Toruń, Poland.
Wojciech BiernatDepartment of Pathomorphology, Medical University of Gdańsk, Gdańsk, Poland.
Łukasz SzylbergDepartment of Tumor Pathology and Pathomorphology, Oncology Center - Prof. Franciszek Łukaszczyk Memorial Hospital, Bydgoszcz, Poland.
Piotr RemiszewskiDepartment of Oncological, Transplant and General Surgery, Medical University of Gdańsk, Gdańsk, Poland.
Jakub Mieczkowski3P-Medicine Laboratory, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland.
Natalia Filipowicz3P-Medicine Laboratory, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland. natalia.filipowicz@gumed.edu.pl.
Jan P Dumanski3P-Medicine Laboratory, Medical University of Gdańsk, Dębinki 7, 80-211, Gdańsk, Poland. jan.dumanski@igp.uu.se.
Gdańsk Medical University · PLUppsala University · SENicolaus Copernicus University · PLCollegium Medicum in Bydgoszcz · PLMemorial Hospital · USScience for Life Laboratory · SE

Funding

Fundacja na rzecz Nauki Polskiej MAB/2018 /6Hjärt-Lungfonden grant number 20210051Swedish Research Council 2020-02010
6 · The paper itself

Abstract

Male sex is a risk factor for colorectal cancer (CRC) with higher illness burden and earlier onset. Thus, we hypothesized that loss of chromosome Y (LOY) in the tumor micro-environment (TME) might be involved in oncogenesis. Previous studies show that LOY in circulating leukocytes of aging men was associated with shorter survival and non-hematological cancer, as well as higher LOY in CD4 + T-lymphocytes in men with prostate cancer vs. controls. However, nothing is known about LOY in leukocytes infiltrating TME and we address this aspect here. We studied frequency and functional effects of LOY in blood, TME and non-tumorous tissue. Regulatory T-lymphocytes (Tregs) in TME had the highest frequency of LOY (22%) in comparison to CD4 + T-lymphocytes and cytotoxic CD8 + T-lymphocytes. LOY score using scRNA-seq was also linked to higher expression of PDCD1, TIGIT and IKZF2 in Tregs. PDCD1 and TIGIT encode immune checkpoint receptors involved in the regulation of Tregs function. Our study sets the direction for further functional research regarding a probable role of LOY in intensifying features related to the suppressive phenotype of Tregs in TME and consequently a possible influence on immunotherapy response in CRC patients.

Indexed as

Colorectal NeoplasmsLiver NeoplasmsT-Lymphocytes, RegulatoryTumor MicroenvironmentAgedFemaleHumansIkaros Transcription FactorLymphocytes, Tumor-InfiltratingMaleMiddle AgedProgrammed Cell Death 1 ReceptorReceptors, ImmunologicIkaros Transcription FactorPDCD1 protein, humanProgrammed Cell Death 1 ReceptorReceptors, ImmunologicTIGIT protein, human

Identifiers

PMID38658633
PMCPMC11043399
OpenAlexW4395071285

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.