Evidence map›Paper›PMID 35459193›Full record

ArticleJournal of experimental & clinical cancer research : CR2022

RORγt agonist enhances anti-PD-1 therapy by promoting monocyte-derived dendritic cells through CXCL10 in cancers.

Li Xia, Enming Tian, Mingcheng Yu, Chenglong Liu, Lian Shen, Yafei Huang, Zhongen Wu, Jinlong Tian, Ker Yu, Yonghui Wang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.0field-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

25 citing papers in PubMed, 42 citations in OpenAlex.

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  20. Small-molecule agents for cancer immunotherapy.Acta pharmaceutica Sinica. B · 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

12 authors at 2 institutions in 1 country.

Li Xia *Department of Pharmacology, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Enming Tian *Department of Pharmacology, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Mingcheng YuDepartment of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Chenglong LiuDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Lian ShenDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Yafei HuangDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Zhongen WuDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Jinlong TianDepartment of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Ker YuDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Yonghui WangDepartment of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Qiong XieDepartment of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai, 201203, China.
Di ZhuDepartment of Pharmacology, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China. zhudi@fudan.edu.cn.ORCID http://orcid.org/0000-0003-4622-4600
Fudan University · CNShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe overall response rate to checkpoint blockade remains unsatisfactory, partially due to the immune-suppressive tumor microenvironment. A retinoic acid-related orphan receptor γt (RORγt) agonist (LYC-55716) is currently used in clinical trials combined with anti-PD-1, but how the Th17 cell transcription factor RORγt enhances antitumor immunity of PD-1 in the tumor microenvironment remains elusive.

methodsThe expression of mRNA was analyzed using qPCR assays. Flow cytometry was used to sort and profile cells. Cell migration was analyzed using Transwell assays. Biacore was used to determine the binding affinity to the RORγt protein. The RORγt GAL4 cell-based reporter gene assay was used to measure activity in the RORγt driven luciferase reporter gene expression.

resultsWe designed a potent and selective small-molecule RORγt agonist (8-074) that shows robust antitumor efficacy in syngeneic tumor models and improves the efficacy of anti‑PD‑1 in a murine lung cancer model. RORγt agonist treatment increased intratumoral CD8

conclusionOur results revealed that the RORγt agonist improved the efficacy of anti-PD-1. The RORγt agonist increased the migration of MoDCs, which increased the local levels of CXCL10, thus promoting CD8

Indexed as

CD8-Positive T-LymphocytesLung NeoplasmsAnimalsChemokine CXCL10Dendritic CellsHumansMiceMonocytesNuclear Receptor Subfamily 1, Group F, Member 3Programmed Cell Death 1 ReceptorTumor MicroenvironmentChemokine CXCL10CXCL10 protein, humanNuclear Receptor Subfamily 1, Group F, Member 3Programmed Cell Death 1 ReceptorCXCL10ImmunotherapyRORγtTh17Tumor microenvironment

Identifiers

PMID35459193
PMCPMC9034499
OpenAlexW4224324242

What OpenQuestion holds

Textmetadata
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.