Evidence map›Paper›PMID 38427437›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2024

Radiotherapy Enhances Metastasis Through Immune Suppression by Inducing PD-L1 and MDSC in Distal Sites.

Yuzhu Hou, Kaiting Yang, Liangliang Wang, Jiaai Wang, Xiaona Huang, András Piffkó, Sean Z Luo, Xinshuang Yu, Enyu Rao, Carlos Martinez and 7 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
10.8field-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

40 citing papers in PubMed, 45 citations in OpenAlex.

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  15. CXCR5Nature communications · 2026
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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

17 authors at 2 institutions in 3 countries.

Yuzhu Hou *Department of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, ShaanXi, China.ORCID 0000-0001-8274-027X
Kaiting YangDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0001-9328-5655
Liangliang WangDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0001-8340-5190
Jiaai WangDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0003-3217-7444
Xiaona HuangDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0002-9983-5723
András PiffkóDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0001-5300-6594
Sean Z LuoDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0009-0006-8652-8827
Xinshuang YuDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0001-9095-3435
Enyu RaoDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0003-2949-2902
Carlos MartinezDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0002-6934-9847
Jason BugnoDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0002-3046-8072
Matthias MackDepartment of Nephrology, University Hospital Regensburg, Regensburg, Germany.ORCID 0000-0002-3157-7262
Everett E VokesDepartment of Medicine, University of Chicago, Chicago, Illinois.ORCID 0000-0002-8645-8068
Sean P PitrodaDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0003-3056-7991
Steven J ChmuraDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0001-8851-7108
Ralph R WeichselbaumDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0002-5643-8939
Hua Laura Liang *Department of Radiation and Cellular Oncology, University of Chicago, Chicago, Illinois.ORCID 0000-0001-5512-8595
University of Illinois Chicago · USUniversity Hospital Regensburg · DE

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI CHIEN-MIN KAO · 1985 to 2026
$122.1M
Developing an Oncology Workforce for the 21st Century - Renewal 01K12CA139160 · NCI · UNIVERSITY OF CHICAGO · PI OLOPADE, OLUFUNMILAYO F., SMITH, SONALI · 2010 to 2024
$10.6M
Radiation Effect on Immune Cells and the MicrobiomeU54CA274291 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI Joseph O Deasy, Silvia C. Formenti · 2022 to 2026
$9.1M
CLINICAL THERAPEUTICST32GM007019 · NIGMS · UNIVERSITY OF CHICAGO · PI Peter Hugh O'Donnell, MARK J RATAIN · 1985 to 2026
$8.7M
Elucidating the Roles of RNA m6A readers Y1 and Y2 in radiation-induced immunity and immunotherapyR01CA262508 · NCI · UNIVERSITY OF CHICAGO · PI WEICHSELBAUM, RALPH R · 2021 to 2025
$2.0M
Therapeutic use of T cells engineered to produce radiation-inducible cytokinesR21CA226582 · NCI · UNIVERSITY OF CHICAGO · PI WEICHSELBAUM, RALPH R · 2019 to 2020
$388k
NCI NIH HHS K12 CA139160NCI NIH HHS P30 CA014599NCI NIH HHS R01 CA262508NCI NIH HHS R21 CA226582NCI NIH HHS U54 CA274291NIGMS NIH HHS T32 GM007019
6 · The paper itself

Abstract

purposeRadiotherapy (RT) is a widely employed anticancer treatment. Emerging evidence suggests that RT can elicit both tumor-inhibiting and tumor-promoting immune effects. The purpose of this study is to investigate immune suppressive factors of radiotherapy. EXPERIMENTAL

designWe used a heterologous two-tumor model in which adaptive concomitant immunity was eliminated.

resultsThrough analysis of PD-L1 expression and myeloid-derived suppressor cells (MDSC) frequencies using patient peripheral blood mononuclear cells and murine two-tumor and metastasis models, we report that local irradiation can induce a systemic increase in MDSC, as well as PD-L1 expression on dendritic cells and myeloid cells, and thereby increase the potential for metastatic dissemination in distal, nonirradiated tissue. In a mouse model using two distinct tumors, we found that PD-L1 induction by ionizing radiation was dependent on elevated chemokine CXCL10 signaling. Inhibiting PD-L1 or MDSC can potentially abrogate RT-induced metastasis and improve clinical outcomes for patients receiving RT.

conclusionsBlockade of PD-L1/CXCL10 axis or MDSC infiltration during irradiation can enhance abscopal tumor control and reduce metastasis.

Indexed as

B7-H1 AntigenMyeloid-Derived Suppressor CellsAnimalsCell Line, TumorChemokine CXCL10Disease Models, AnimalFemaleHumansMiceNeoplasm MetastasisB7-H1 AntigenCD274 protein, humanChemokine CXCL10

Identifiers

PMID38427437
PMCPMC11062826
OpenAlexW4392388168

What OpenQuestion holds

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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.