Evidence map›Paper›PMID 33570246›Full record

ArticleCancer communications (London, England)2021

Insulin gene enhancer protein 1 mediates glycolysis and tumorigenesis of gastric cancer through regulating glucose transporter 4.

Ting Guo, Yan-Hua Bai, Xiao-Jing Cheng, Hai-Bo Han, Hong Du, Ying Hu, Shu-Qin Jia, Xiao-Fang Xing, Jia-Fu Ji

Open access · goldAbstract read
In one paragraph

Article in Cancer communications (London, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. [Development and dissemination of precision medicine approaches in gastric cancer management].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
    Article
  5. Article
  6. Article
  7. Energy metabolism in health and diseases.Signal transduction and targeted therapy · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Energy metabolism: a new target for gastric cancer treatment.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  15. N6-methyladenosine modification of OIP5-AS1 promotes glycolysis, tumorigenesis, and metastasis of gastric cancer by inhibiting Trim21-mediated hnRNPA1 ubiquitination and degradation.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2024
    Article
  16. Article
  17. Article
  18. Ubiquitous mitochondrial creatine kinase promotes the progression of gastric cancer through a JNK-MAPK/JUN/HK2 axis regulated glycolysis.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2023
    Article
  19. Saponins fromNutrients · 2022
    Article
  20. 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

9 authors at 1 institution in 1 country.

Ting GuoKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Division of Gastrointestinal Cancer Translational Research Laboratory, Peking University Cancer Hospital & Institute, Beijing, 100142, P. R. China.ORCID 0000-0003-0199-5639
Yan-Hua BaiDepartment of Pathology, Peking University Cancer Hospital & Institute, Beijing, 100142, P. R. China.ORCID 0000-0002-7634-282X
Xiao-Jing ChengKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Division of Gastrointestinal Cancer Translational Research Laboratory, Peking University Cancer Hospital & Institute, Beijing, 100142, P. R. China.ORCID 0000-0002-5467-791X
Hai-Bo HanThe Tissue Bank, Peking University Cancer Hospital & Institute, Beijing, 100142, P. R. China.ORCID 0000-0003-2240-5546
Hong DuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Division of Gastrointestinal Cancer Translational Research Laboratory, Peking University Cancer Hospital & Institute, Beijing, 100142, P. R. China.ORCID 0000-0002-1107-2902
Ying HuThe Tissue Bank, Peking University Cancer Hospital & Institute, Beijing, 100142, P. R. China.ORCID 0000-0002-6330-8032
Shu-Qin JiaDepartment of Molecular Diagnosis, Peking University Cancer Hospital & Institute, Beijing, 100142, P. R. China.ORCID 0000-0001-6688-0408
Xiao-Fang XingKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Division of Gastrointestinal Cancer Translational Research Laboratory, Peking University Cancer Hospital & Institute, Beijing, 100142, P. R. China.ORCID 0000-0002-5707-3396
Jia-Fu JiKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Division of Gastrointestinal Cancer Translational Research Laboratory, Peking University Cancer Hospital & Institute, Beijing, 100142, P. R. China.ORCID 0000-0001-6878-5543
Peking University · CN

Funding

Beijing Municipal Administration of Hospitals' Youth Program QML20181102Interdisciplinary Medicine Seed Fund of Peking University BMU2018MX018National High Technology Research and Development Program of China 2014AA020603National Natural Science Foundation of China 81301874National Natural Science Foundation of China 81802471National Natural Science Foundation of China 81872502National Natural Science Foundation of China 81972758Natural Science Foundation of Beijing 7132051Science Foundation of Peking University Cancer Hospital 2017-23Science Foundation of Peking University Cancer Hospital 2020-6
6 · The paper itself

Abstract

backgroundInsulin gene enhancer protein 1, (ISL1), a LIM-homeodomain transcription factor, is involved in multiple tumors and is associated with insulin secretion and metabolic phenotypes. However, the role of ISL1 in stimulating glycolysis to promote tumorigenesis in gastric cancer (GC) is unclear. In this study, we aimed to characterize the expression pattern of ISL1 in GC patients and explore its molecular biological mechanism in glycolysis and tumorigenesis.

methodsWe analyzed the expression and clinical significance of ISL1 in GC using immunohistochemistry and real-time polymerase chain reaction (PCR). Flow cytometry and IncuCyte assays were used to measure cell proliferation after ISL1 knockdown. RNA-sequencing was performed to identify differentially expressed genes, followed by Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis and Gene Set Enrichment Analysis (GSEA) to reveal key signaling pathways likely regulated by ISL1 in GC. Alteration of the glycolytic ability of GC cells with ISL1 knockdown was validated by measuring the extracellular acidification rate (ECAR) and oxygen consumption rate (OCR) and by detecting glucose consumption and lactate production. The expression of glucose transporter 4 (GLUT4) and ISL1 was assessed by Western blotting, immunohistochemistry, and immunofluorescent microscopy. The luciferase reporter activity and chromatin immunoprecipitation assays were performed to determine the transcriptional regulation of ISL1 on GLUT4.

resultsHigh levels of ISL1 and GLUT4 expression was associated with short survival of GC patients. ISL1 knockdown inhibited cell proliferation both in vitro and in vivo. KEGG analysis and GSEA for RNA-sequencing data indicated impairment of the glycolysis pathway in GC cells with ISL1 knockdown, which was validated by reduced glucose uptake and lactate production, decreased ECAR, and increased OCR. Mechanistic investigation indicated that ISL1 transcriptionally regulated GLUT4 through binding to its promoter.

conclusionISL1 facilitates glycolysis and tumorigenesis in GC via the transcriptional regulation of GLUT4.

Indexed as

InsulinsStomach NeoplasmsCarcinogenesisCell Line, TumorGlucose Transport Proteins, FacilitativeGlycolysisHumansGlucose Transport Proteins, FacilitativeInsulinsgastric cancerglucose transporter 4glycolysisinsulin gene enhancer protein 1tumorigenesis

Identifiers

PMID33570246
PMCPMC7968886
OpenAlexW3127996126

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.