Evidence map›Paper›PMID 39402618›Full record

ArticleClinical epigenetics2024

PER3 promoter hypermethylation correlates to the progression of pan-cancer.

Yaoxu Li, Wenjuan Li, Jinhai Deng, Mingzhu Yin

Abstract read
In one paragraph

Article in Clinical epigenetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Circadian clock and cancer.Military Medical Research · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. Article
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

4 authors.

Yaoxu Li *Department of Stomatology, Chongqing University Three Gorges Hospital, School of Medicine, Chongqing University, Wanzhou District, Chongqing, 404100, China.
Wenjuan Li *Department of Emergency and Critical Care Medicine, The First Afliated Hospital of Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Jinhai DengClinical Research Center (CRC), Medical Pathology Center (MPC), Cancer Early Detection and Treatment Center (CEDTC) and Translational Medicine Research Center (TMRC), Chongqing University Three Gorges Hospital, School of Medicine, Chongqing University, Wanzhou District, Chongqing, 404100, China.
Mingzhu YinClinical Research Center (CRC), Medical Pathology Center (MPC), Cancer Early Detection and Treatment Center (CEDTC) and Translational Medicine Research Center (TMRC), Chongqing University Three Gorges Hospital, School of Medicine, Chongqing University, Wanzhou District, Chongqing, 404100, China. yinmingzhu2008@126.com.

Funding

Chongqing Natural Science Foundation CSTB2023NSCQ-BHX0047Chongqing Science and Health Joint Scientific Research Project on Traditional Chinese Medicine 2024ZYQN001Chongqing Wanzhou Municipal Science and Health Joint Research Project wzstc-kw2023039Chongqing Wanzhou social science key topics WZKT2024086Natural Science Foundation of Chongqing, China CSTB2024NSCQ-MSX0761the Natural Science Foundation of China 82073020
6 · The paper itself

Abstract

backgroundMalignant cells exhibit reduced period circadian regulator 3 (PER3) expression. However, the underlying mechanisms of variations in PER3 expression in cancers and the specific function of PER3 in tumor progression remain poorly understood.

resultsWe explored multiple public databases, conducted bioinformatics analyses, and performed in vitro and in vivo experiments for validation. We found PER3 expression was decreased in most types of cancers, and PER3 downregulation was associated with a poor prognosis in 8 types of cancer. PER3 promoter methylation levels were increased in 11 types of cancer. Promoter hypermethylation (CpG islands [CGIs] cg12258811 and cg14204433) correlated with decreased PER3 expression in six cancers (breast invasive carcinoma, colon adenocarcinoma, head and neck squamous cell carcinoma, kidney renal papillary cell carcinoma [KIRP], lung adenocarcinoma [LUAD], and uterine corpus endometrial carcinoma). CGI cg12258811 hypermethylation was associated with reduced survival time and advanced cancer stages. Moreover, the bisulfite pyrosequencing assay confirmed CGI cg12258811 hypermethylation and its negative correlation with PER3 expression. In vitro and in vivo experiments demonstrated that PER3 inhibited KIRP and LUAD progression. Decitabine enhanced PER3 expression and inhibited KIRP cell functions by reducing promoter (cg12258811) methylation level.

conclusionsOur findings advanced the mechanistic understanding of variations in PER3 expression in cancers and confirmed the tumor-associated function of PER3 hypermethylation and downregulation.

Indexed as

Disease ProgressionDNA MethylationGene Expression Regulation, NeoplasticNeoplasmsPeriod Circadian ProteinsPromoter Regions, GeneticAnimalsCell Line, TumorCpG IslandsDecitabineDown-RegulationEpigenesis, GeneticFemaleHumansMaleMiceDecitabinePER3 protein, humanPeriod Circadian ProteinsKidney renal papillary cell carcinomaLung adenocarcinomaMethylationPan-cancerPeriod circadian regulator 3Promoter

Identifiers

PMID39402618
PMCPMC11476066

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Registered trials

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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.