Evidence map›Paper›PMID 37210553›Full record

ArticleJournal of experimental & clinical cancer research : CR2023

Chronic psychological stress promotes breast cancer pre-metastatic niche formation by mobilizing splenic MDSCs via TAM/CXCL1 signaling.

Yifeng Zheng, Neng Wang, Shengqi Wang, Juping Zhang, Bowen Yang, Zhiyu Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 3 pooled it
12.7field-weighted citation impact, top 1% 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

47 citing papers in PubMed, 3 syntheses or guidelines pooled it, 57 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

6 authors at 1 institution in 1 country.

Yifeng Zheng *State Key Laboratory of Dampness Syndrome of Chinese Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Neng Wang *Integrative Research Laboratory of Breast Cancer, Discipline of Integrated Chinese and Western Medicine, The Second Clinical College of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, 510006, China.
Shengqi WangState Key Laboratory of Dampness Syndrome of Chinese Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Juping ZhangState Key Laboratory of Dampness Syndrome of Chinese Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Bowen YangState Key Laboratory of Dampness Syndrome of Chinese Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Zhiyu WangState Key Laboratory of Dampness Syndrome of Chinese Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510006, China. wangzhiyu@gzucm.edu.cn.ORCID http://orcid.org/0000-0002-5299-8410
Guangzhou University of Chinese Medicine · CN

Funding

Foundation for Young Scholars of Guangzhou University of Chinese Medicine QNYC20190101Guangdong Medical Research Foundation 20201119103046743Guangzhou Municipal Science and Technology Project 201904010407Guangzhou Municipal Science and Technology Project 202102010241Guangzhou Municipal Science and Technology Project 202102010316Guangzhou Municipal Science and Technology Project 202201020357National Natural Science Foundation of China 81873306National Natural Science Foundation of China 81973526National Natural Science Foundation of China 82004132National Natural Science Foundation of China 82004373National Natural Science Foundation of China 82074165National Natural Science Foundation of China 82174165Research Fund for Bajian Talents of Guangdong Provincial Hospital of Chinese Medicine BJ2022KY12Research Fund for Bajian Talents of Guangdong Provincial Hospital of Chinese Medicine BJ2022KY18Science and Technology Planning Project of Guangdong Province 2017B030314166Science and Technology Planning Project of Guangdong Province 2021A0505030059Science and Technology Planning Project of Guangdong Province 2022A1515011412State Key Laboratory of Dampness Syndrome of Chinese Medicine SZ2021ZZ19The 2020 Guangdong Provincial Science and Technology Innovation Strategy Special Fund (Guangdong-Hong Kong-Macau Joint Lab) 2020B1212030006The Specific Research Fund for TCM Science and Technology of Guangdong provincial Hospital of Chinese Medicine YN2018MJ07The Specific Research Fund for TCM Science and Technology of Guangdong provincial Hospital of Chinese Medicine YN2018QJ08Traditional Chinese Medicine Bureau of Guangdong Province 20212085Traditional Chinese Medicine Bureau of Guangdong Province 20225011
6 · The paper itself

Abstract

backgroundEmerging studies have identified chronic psychological stress as an independent risk factor influencing breast cancer growth and metastasis. However, the effects of chronic psychological stress on pre-metastatic niche (PMN) formation and the underlying immunological mechanisms remain largely unknown.

methodsThe effects and molecular mechanisms of chronic unpredictable mild stress (CUMS) on modulating tumor-associated macrophages (TAMs) and PMN formation were clarified by multiplex immunofluorescence technique, cytokine array, chromatin immunoprecipitation, the dual-luciferase reporter assay, and breast cancer xenografts. Transwell and CD8

resultsCUMS significantly promoted breast cancer growth and metastasis, accompanied by TAMs accumulation in the microenvironment. CXCL1 was identified as a crucial chemokine in TAMs facilitating PMN formation in a glucocorticoid receptor (GR)-dependent manner. Interestingly, the spleen index was significantly reduced under CUMS, and splenic MDSCs were validated as a key factor mediating CXCL1-induced PMN formation. The molecular mechanism study revealed that TAM-derived CXCL1 enhanced the proliferation, migration, and anti-CD8

conclusionOur findings shed new light on the association between chronic psychological stress and splenic MDSC mobilization, and suggest that stress-related glucocorticoid elevation can enhance TAM/CXCL1 signaling and subsequently recruit splenic MDSCs to promote PMN formation via CXCR2.

Indexed as

Breast NeoplasmsMelanomaMyeloid-Derived Suppressor CellsStress, PsychologicalChemokine CXCL1Cutaneous Malignant MelanomaFemaleHumansSpleenTumor MicroenvironmentChemokine CXCL1CXCL1 protein, humanBreast cancerChronic psychological stressCXCL1/CXCR2Myeloid-derived suppressor cellsPre-metastatic niche

Identifiers

PMID37210553
PMCPMC10199643
OpenAlexW4377157777

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.