Evidence map›Paper›PMID 32012400›Full record

ArticleCancer science2020

Tumor cell-derived angiopoietin-like protein 2 establishes a preference for glycolytic metabolism in lung cancer cells.

Hironobu Osumi, Haruki Horiguchi, Tsuyoshi Kadomatsu, Kyosei Tashiro, Jun Morinaga, Takashi Takahashi, Koei Ikeda, Takaaki Ito, Makoto Suzuki, Motoyoshi Endo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. 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

11 authors at 4 institutions in 1 country.

Hironobu OsumiDepartment of Molecular Genetics, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan.
Haruki HoriguchiDepartment of Molecular Genetics, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan.ORCID https://orcid.org/0000-0001-9344-8362
Tsuyoshi KadomatsuDepartment of Molecular Genetics, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan.ORCID https://orcid.org/0000-0003-3327-6954
Kyosei TashiroDepartment of Molecular Genetics, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan.
Jun MorinagaDepartment of Molecular Genetics, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan.
Takashi TakahashiAichi Cancer Center, Nagoya, Japan.
Koei IkedaDepartment of Thoracic Surgery, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan.
Takaaki ItoDepartment of Pathology and Experimental Medicine, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan.
Makoto SuzukiDepartment of Thoracic Surgery, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan.
Motoyoshi EndoDepartment of Molecular Biology, University of Occupational and Environmental Health, Kitakyushu, Japan.
Yuichi OikeDepartment of Molecular Genetics, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan.
Kumamoto University · JPKumamoto Health Science University · JPAichi Cancer Center · JPUniversity of Occupational and Environmental Health Japan · JP

Funding

Core Research for Evolutional Science and Technology 13417915CREST program of the Japan Agency for Medical Research and Development (AMED) JP19gm0610007Ministry of Education, Culture, Sports, Science and Technology 17K08663Ministry of Education, Culture, Sports, Science and Technology 18K07236Ministry of Education, Culture, Sports, Science and Technology 18K15246Takeda Science Foundation
6 · The paper itself

Abstract

We previously revealed that tumor cell-derived angiopoietin-like protein 2 (ANGPTL2) accelerates the metastatic capacity of tumors in an autocrine/paracrine manner by activating tumor cell motility and invasiveness and the epithelial-mesenchymal transition. However, the effects of ANGPTL2 on cancer cell glycolytic metabolism, which is a hallmark of tumor cells, are unknown. Here we report evidence supporting a role for tumor cell-derived ANGPTL2 in establishing a preference for glycolytic metabolism. We report that a highly metastatic lung cancer cell subline expressing abundant ANGPTL2 showed upregulated expression of the glucose transporter GLUT3 as well as enhanced glycolytic metabolism relative to a less metastatic parental line. Most notably, ANGPTL2 overexpression in the less metastatic line activated glycolytic metabolism by increasing GLUT3 expression. Moreover, ANGPTL2 signaling through integrin α5β1 increased GLUT3 expression by increasing transforming growth factor-β (TGF-β) signaling and expression of the downstream transcription factor zinc finger E-box binding homeobox 1 (ZEB1). Conversely, ANGPTL2 knockdown in the highly metastatic subline decreased TGF-β1, ZEB1, and GLUT3 expression and antagonized glycolytic metabolism. In primary tumor cells from patients with lung cancer, ANGPTL2 expression levels correlated with GLUT3 expression. Overall, this work suggests that tumor cell-derived ANGPTL2 accelerates activities associated with glycolytic metabolism in lung cancer cells by activating TGF-β-ZEB1-GLUT3 signaling.

Indexed as

Angiopoietin-Like Protein 2Angiopoietin-like ProteinsAutocrine CommunicationCell Line, TumorCell MovementCell ProliferationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticGlucose Transporter Type 3GlycolysisHumansIntegrin alpha5beta1Lung NeoplasmsMaleNeoplasm InvasivenessAngiopoietin-Like Protein 2Angiopoietin-like ProteinsANGPTL2 protein, humanGlucose Transporter Type 3Integrin alpha5beta1SLC2A3 protein, humanTransforming Growth Factor betaZEB1 protein, humanZinc Finger E-box-Binding Homeobox 1ANGPTL2cancer metabolismGLUT3lung cancerZEB1

Identifiers

PMID32012400
PMCPMC7156862
OpenAlexW3004952763

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.