Evidence map›Paper›PMID 35246476›Full record

ArticleJournal for immunotherapy of cancer2022

System analysis based on the cancer-immunity cycle identifies ZNF207 as a novel immunotherapy target for hepatocellular carcinoma.

Xu Wang, Tao Zhou, Xingyi Chen, Yu Wang, Yushi Ding, Haoyang Tu, Shengyang Gao, Haoyu Wang, Xinying Tang, Yong Yang

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 28 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

10 authors at 1 institution in 1 country.

Xu Wang *State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China.
Tao Zhou *State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China.
Xingyi Chen *State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China.
Yu WangState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China.
Yushi DingState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China.
Haoyang TuState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China.
Shengyang GaoState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China.
Haoyu WangState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China.
Xinying TangState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China yy@cpu.edu.cn 1620174466@cpu.edu.cn.
Yong YangState Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China yy@cpu.edu.cn 1620174466@cpu.edu.cn.ORCID 0000-0002-2841-8420
China Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors as monotherapies for advanced hepatocellular carcinoma (HCC) fail to achieve satisfying results, while combination therapies show greater efficacy. Therefore, identifying new combined targets for immune checkpoint inhibitors could be promising.

methodsWe combined the cancer-immunity cycle score with weighted gene coexpression network and system analyses to screen immunosuppressive targets in HCC. In vitro and in vivo experiments were used to assess the effect of zinc finger protein 207 (ZNF207) on HCC immunity. RNA sequencing, metabolomic, cytokine array analysis, dual-luciferase reporter gene assay, and ChIP quantitative PCR assay were used to investigate the role of ZNF207 in tumor immunity regulation.

resultsThe system analysis and experimental verification revealed ZNF207 as an immunosuppressive target in HCC. Hypoxia-induced upregulation of ZNF207 promoted HCC progression in immunocompetent mice while being associated with decreased CD8

conclusionOur study implicates ZNF207 in suppressing the HCC microenvironment and showed the feasibility of targeting ZNF207 during anti-PD1 therapy in HCC.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAnimalsCD8-Positive T-LymphocytesHumansImmune Checkpoint InhibitorsImmunotherapyMiceMicrotubule-Associated ProteinsTumor MicroenvironmentImmune Checkpoint InhibitorsMicrotubule-Associated ProteinsZNF207 protein, humancombined modality therapycomputational biologyimmunotherapyliver neoplasmstumor microenvironment

Identifiers

PMID35246476
PMCPMC8900045
OpenAlexW4214869547

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.