Evidence map›Paper›PMID 36176733›Full record

ReviewMedComm2022

Targeting epigenetic regulators for inflammation: Mechanisms and intervention therapy.

Su Zhang, Yang Meng, Lian Zhou, Lei Qiu, Heping Wang, Dan Su, Bo Zhang, Kui-Ming Chan, Junhong Han

Open access · goldAbstract readReview
In one paragraph

Review in MedComm, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

55 citing papers in PubMed, 63 citations in OpenAlex.

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  7. Caspase-1 in cancer and inflammatory diseases: a potential therapeutic target.Apoptosis : an international journal on programmed cell death · 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

9 authors at 3 institutions in 2 countries.

Su ZhangLaboratory of Cancer Epigenetics and Genomics Frontiers Science Center for Disease-Related Molecular Network State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu China.
Yang MengLaboratory of Cancer Epigenetics and Genomics Frontiers Science Center for Disease-Related Molecular Network State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu China.
Lian ZhouLaboratory of Cancer Epigenetics and Genomics Frontiers Science Center for Disease-Related Molecular Network State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu China.
Lei QiuLaboratory of Cancer Epigenetics and Genomics Frontiers Science Center for Disease-Related Molecular Network State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu China.ORCID https://orcid.org/0000-0002-0202-4618
Heping WangDepartment of Neurosurgery Tongji Hospital of Tongji Medical College Huazhong University of Science and Technology Wuhan China.
Dan SuLaboratory of Cancer Epigenetics and Genomics Frontiers Science Center for Disease-Related Molecular Network State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu China.
Bo ZhangLaboratory of Cancer Epigenetics and Genomics Department of Gastrointestinal Surgery Frontiers Science Center for Disease-Related Molecular Network West China Hospital Sichuan University Chengdu China.
Kui-Ming ChanDepartment of Biomedical Sciences City University of Hong Kong Hong Kong China.
Junhong HanLaboratory of Cancer Epigenetics and Genomics Frontiers Science Center for Disease-Related Molecular Network State Key Laboratory of Biotherapy West China Hospital Sichuan University Chengdu China.ORCID https://orcid.org/0000-0002-3371-8698
Sichuan University · CNCity University of Hong Kong · HKTongji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence indicates that resolution of inflammation is a critical and dynamic endogenous process for host tissues defending against external invasive pathogens or internal tissue injury. It has long been known that autoimmune diseases and chronic inflammatory disorders are characterized by dysregulated immune responses, leading to excessive and uncontrol tissue inflammation. The dysregulation of epigenetic alterations including DNA methylation, posttranslational modifications to histone proteins, and noncoding RNA expression has been implicated in a host of inflammatory disorders and the immune system. The inflammatory response is considered as a critical trigger of epigenetic alterations that in turn intercede inflammatory actions. Thus, understanding the molecular mechanism that dictates the outcome of targeting epigenetic regulators for inflammatory disease is required for inflammation resolution. In this article, we elucidate the critical role of the nuclear factor-κB signaling pathway, JAK/STAT signaling pathway, and the NLRP3 inflammasome in chronic inflammatory diseases. And we formulate the relationship between inflammation, coronavirus disease 2019, and human cancers. Additionally, we review the mechanism of epigenetic modifications involved in inflammation and innate immune cells. All that matters is that we propose and discuss the rejuvenation potential of interventions that target epigenetic regulators and regulatory mechanisms for chronic inflammation-associated diseases to improve therapeutic outcomes.

Indexed as

epigenetic regulatorimmuneinflammationposttranslational modification (PTM)

Identifiers

PMID36176733
PMCPMC9477794
OpenAlexW4296195278

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.