Evidence map›Paper›PMID 38427147›Full record

ArticleJournal of gastrointestinal cancer2024

Biological Clock Genes are Crucial and Promising Biomarkers for the Therapeutic Targets and Prognostic Assessment in Gastric Cancer.

Yonggang Tian, Yunqian Xie, Feihu Bai, Jun Wang, Dekui Zhang

Abstract read
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In one paragraph

Article in Journal of gastrointestinal cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
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

5 authors at 3 institutions in 1 country.

Yonggang Tian *Department of Gastroenterology, Lanzhou University Second Hospital, Cuiyingmen No. 82, Chengguan District, Lanzhou, 730030, Gansu Province, China.
Yunqian Xie *The Gastroenterology Clinical Medical Center of Hainan Province, Department of Gastroenterology, The Second Affiliated Hospital of Hainan Medical University, Hainan Province, Haikou City, China.
Feihu BaiThe Gastroenterology Clinical Medical Center of Hainan Province, Department of Gastroenterology, The Second Affiliated Hospital of Hainan Medical University, Hainan Province, Haikou City, China. baifeihu@sohu.com.
Jun WangDepartment of Gastroenterology, 986 Hospital, Xijing Hospital, Air Force Military Medical University, No. 269, Youyi East Road, Xi'an, Shaanxi Province, 710089, China. wangjundoctor@aliyun.com.
Dekui ZhangDepartment of Gastroenterology, Lanzhou University Second Hospital, Cuiyingmen No. 82, Chengguan District, Lanzhou, 730030, Gansu Province, China. zhangdk8616@126.com.
Hainan Medical University · CNLanzhou University · CNXijing Hospital · CN

Funding

Hainan Province Clinical Medical Center 2021818Hainan Provincial Health Industry Research Project 22A200078Medical Innovation and Development Project of Lanzhou University lzuyxcx-2022-181the specific research fund of The Innovation Platform for Academicians of Hainan Province 2022136
6 · The paper itself

Abstract

backgroundGastric cancer is one of the major public health problems worldwide. Circadian rhythm disturbances driven by circadian clock genes play a role in the development of cancer. However, whether circadian clock genes can serve as potential therapeutic targets and prognostic biomarkers for gastric cancer remains elusive.

methodsIn this study, we comprehensively analyzed the potential relationship between circadian clock genes and gastric cancer using online bioinformatics databases such as GEPIA, cBioPortal, STRING, GeneMANIA, Metascape, TIMER, TRRUST, and GEDS.

resultsBiological clock genes are expressed differently in human tumors. Compared with normal tissues, only PER1, CLOCK, and TIMELESS expression differences were statistically significant in gastric cancer (p < 0.05). PER1 (p = 0.0169) and CLOCK (p = 0.0414) were associated with gastric cancer pathological stage (p < 0.05). Gastric cancer patients with high expression of PER1 (p = 0.0028) and NR1D1 (p = 0.016) had longer overall survival, while those with high expression of PER1 (p = 0.042) and NR1D1 (p = 0.016) had longer disease-free survival. The main function of the biological clock gene is related to the circadian rhythms and melatonin metabolism and effects. CLOCK, NPAS2, and KAT2B were key transcription factors for circadian clock genes. In addition, we also found important correlations between circadian clock genes and various immune cells in the gastric cancer microenvironment.

conclusionsThis study may establish a new gastric cancer prognostic indicator based on the biological clock gene and develop new drugs for the treatment of gastric cancer using biological clock gene targets.

Indexed as

Biomarkers, TumorCLOCK ProteinsStomach NeoplasmsCell Cycle ProteinsCircadian ClocksCircadian RhythmComputational BiologyGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsNuclear Receptor Subfamily 1, Group D, Member 1Period Circadian ProteinsPrognosisBiomarkers, TumorCell Cycle ProteinsCLOCK protein, humanCLOCK ProteinsIntracellular Signaling Peptides and ProteinsNR1D1 protein, humanNuclear Receptor Subfamily 1, Group D, Member 1PER1 protein, humanPeriod Circadian ProteinsTIMELESS protein, humanBioinformaticsBiological clock genesGastric adenocarcinomaGenetic alterationsSignaling pathwaysTumor microenvironment

Identifiers

PMID38427147
OpenAlexW4392360092

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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.