Evidence map›Paper›PMID 37275880›Full record

ArticleFrontiers in immunology2023

The circadian rhythm key gene

Gujie Wu, Hefei Ren, Qin Hu, Huiyun Ma, Hongyu Chen, Lin Zhou, Kun Xu, Liang Ding

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. 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
2.2field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Circadian rhythms and lung cancer biology and immunotherapy: Emerging opportunities and challenges.Chinese medical journal pulmonary and critical care medicine · 2026
    Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Cancer biology & therapy · 2025
    Article
  7. Article
  8. Article
  9. Epigenomics · 2024
    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

8 authors at 3 institutions in 1 country.

Gujie WuDepartment of Respiratory medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Hefei RenDepartment of Laboratory Medicine, Changzheng Hospital, Naval Medical University, Shanghai, China.
Qin HuDepartment of Respiratory medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Huiyun MaDepartment of Respiratory medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Hongyu ChenDepartment of Respiratory medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Lin ZhouDepartment of Respiratory medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Kun XuDepartment of Chemotherapy, Jiangsu Cancer Hospital, Nanjing Medical University, Nanjing, China.
Liang DingDepartment of Respiratory medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Nantong University · CNJiangsu Cancer Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Aryl hydrocarbon receptor nuclear translocator-like 2 (ARNTL2) belongs to the b HLH- PAS domain transcription factor family and is one of the key clock genes that control the circadian rhythm. ARNTL2 plays an important role in human biological functions. However, its role in various tumors, especially in the tumor immune microenvironment (TIME) and immunotherapy, remains unclear. Methods: We integrated data from cancer patients from multiple databases, including the Cancer Genome Atlas, Cancer Cell Lineage Encyclopedia, Genotype Tissue Expression, Human Protein Atlas, cBioPortal, TIMER, and ImmuCellAI, with data from a large clinical study, three immunotherapy cohorts, and Results: ARNTL2 displayed abnormal expression within most malignant tumors, and is significantly associated with poorer survival and pathologic staging. Through gene-set enrichment analysis (GSEA) and gene-set variation analysis (GSVA), we found that ARNTL2 not only regulates cell cycle-related functions to promote cell proliferation but also regulates autoimmunity-related functions of the innate and adaptive immune systems, and other immune-related signaling pathways. In addition, ARNTL2 overexpression contributes to an immunosuppressive tumor microenvironment that plays a key role in immunosuppression-related features, such as the expression of immunosuppression-related genes and pathways and the number of immunosuppressive-infiltrating cells, including regulatory T cells (Tregs), tumor-associated macrophages (TAMs), and cancer-associated fibroblasts (CAFs). The group of patients with low ARNTL2 expression who received immune checkpoint inhibitors (ICI) therapy had better response rates and longer survival when compared to those with high ARNTL2 expression. Conclusion: The findings of this study suggest that ARNTL2 is a potential human oncogene that plays an important role in tumorigenesis and cancer immunity. Elevated ARNTL2 expression indicates an immunosuppressive tumor microenvironment. Targeting ARNTL2 in combination with ICI therapy could bring more significant therapeutic benefits to patients with cancer. Our study sheds light on the remarkable potential of ARNTL2 in tumor immunity and provides a novel perspective for anti-tumor strategies.

Indexed as

ARNTL Transcription FactorsBiomarkers, TumorNeoplasmsTumor MicroenvironmentBiomarkersCell Line, TumorHumansImmunotherapyPrognosisProtein Interaction MapsSignal TransductionTreatment OutcomeUp-RegulationARNTL Transcription FactorsBiomarkersBiomarkers, TumorBMAL2 protein, humanARNTL2human cancersimmunosuppressive tumor microenvironmentimmunotherapyprognosis

Identifiers

PMID37275880
PMCPMC10237319
OpenAlexW4377138698

What OpenQuestion holds

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LicenceCC BY
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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.