Evidence map›Paper›PMID 38331927›Full record

ReviewClinical epigenetics2024

The interaction between DNA methylation and tumor immune microenvironment: from the laboratory to clinical applications.

Daoqi Zhu, Siying Zeng, Chao Su, Jingjun Li, Yiwen Xuan, Yongkai Lin, Enwu Xu, Qin Fan

Open access · goldAbstract readReview
In one paragraph

Review in Clinical epigenetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
10.3field-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

43 citing papers in PubMed, 44 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

8 authors at 3 institutions in 1 country.

Daoqi ZhuSchool of Traditional Chinese Medicine, Southern Medical University, No. 1023 Shatai North Road, Guangzhou, 510515, China.
Siying ZengSchool of Traditional Chinese Medicine, Southern Medical University, No. 1023 Shatai North Road, Guangzhou, 510515, China.
Chao SuSchool of Traditional Chinese Medicine, Southern Medical University, No. 1023 Shatai North Road, Guangzhou, 510515, China.
Jingjun LiNanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Yiwen XuanDepartment of Thoracic Surgery, General Hospital of Southern Theater Command, PLA, No.111 Liuhua Road, Guangzhou, 510010, China.
Yongkai LinDepartment of Endocrinology, The First Affiliated Hospital, Traditional Chinese Medicine University of Guangzhou, Guangzhou, 510405, China.
Enwu XuDepartment of Thoracic Surgery, General Hospital of Southern Theater Command, PLA, No.111 Liuhua Road, Guangzhou, 510010, China. xuenwu@hotmail.com.
Qin FanSchool of Traditional Chinese Medicine, Southern Medical University, No. 1023 Shatai North Road, Guangzhou, 510515, China. fqin@163.com.
Southern Medical University · CNGeneral Hospital of Guangzhou Military Command · CNFirst Affiliated Hospital of Guangzhou University of Chinese Medicine · CN

Funding

2022 "Young Science and Technology Talent Recruitment Project" of Guangzhou Science and Technology Association QT20220101163National Natural Science Foundation of China 82074132Natural Science Foundation of Guangdong Province of China 2314050000165Project of Administration of Traditional Chinese Medicine of Guangdong Province of China 20221258Project of General Hospital of Southern Theater Command 2022NZB004Science and Technology Program of Guangzhou 2023A04J1858
6 · The paper itself

Abstract

DNA methylation is a pivotal epigenetic modification that affects gene expression. Tumor immune microenvironment (TIME) comprises diverse immune cells and stromal components, creating a complex landscape that can either promote or inhibit tumor progression. In the TIME, DNA methylation has been shown to play a critical role in influencing immune cell function and tumor immune evasion. DNA methylation regulates immune cell differentiation, immune responses, and TIME composition Targeting DNA methylation in TIME offers various potential avenues for enhancing immune cytotoxicity and reducing immunosuppression. Recent studies have demonstrated that modification of DNA methylation patterns can promote immune cell infiltration and function. However, challenges persist in understanding the precise mechanisms underlying DNA methylation in the TIME, developing selective epigenetic therapies, and effectively integrating these therapies with other antitumor strategies. In conclusion, DNA methylation of both tumor cells and immune cells interacts with the TIME, and thus affects clinical efficacy. The regulation of DNA methylation within the TIME holds significant promise for the advancement of tumor immunotherapy. Addressing these challenges is crucial for harnessing the full potential of epigenetic interventions to enhance antitumor immune responses and improve patient outcomes.

Indexed as

DNA MethylationNeoplasmsEpigenesis, GeneticHumansImmune ToleranceImmunotherapyTumor MicroenvironmentDNA methylationEpigenetic regulationImmune cell functionImmunotherapy challengesTumor immune microenvironment

Identifiers

PMID38331927
PMCPMC10854038
OpenAlexW4391637876

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.