Evidence map›Paper›PMID 28415822›Full record

ArticleOncotarget2017

Interaction between granulin A and enolase 1 attenuates the migration and invasion of human hepatoma cells.

Xiaoliang Chen, Huanli Xu, Ning Wu, Xiujun Liu, Gan Qiao, Shuonan Su, Ye Tian, Ru Yuan, Cong Li, Xiaohui Liu and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Enolase 1, a Moonlighting Protein, as a Potential Target for Cancer Treatment.International journal of biological sciences · 2021
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Progranulin and its biological effects in cancer.Medical oncology (Northwood, London, England) · 2017
    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

11 authors at 3 institutions in 1 country.

Xiaoliang ChenDepartment of Pharmacology, Capital Medical University, Beijing 100069, China.
Huanli XuDepartment of Pharmacology, Capital Medical University, Beijing 100069, China.
Ning WuInstitute of Oceanology, Chinese Academy of Science, Qingdao 266003, China.
Xiujun LiuInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science, Beijing 100050, China.
Gan QiaoDepartment of Pharmacology, Capital Medical University, Beijing 100069, China.
Shuonan SuDepartment of Pharmacology, Capital Medical University, Beijing 100069, China.
Ye TianDepartment of Pharmacology, Capital Medical University, Beijing 100069, China.
Ru YuanDepartment of Pharmacology, Capital Medical University, Beijing 100069, China.
Cong LiDepartment of Pharmacology, Capital Medical University, Beijing 100069, China.
Xiaohui LiuDepartment of Pharmacology, Capital Medical University, Beijing 100069, China.
Xiukun LinDepartment of Pharmacology, Capital Medical University, Beijing 100069, China.
Capital Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNInstitute of Oceanology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Granulin A (GRN A), a peptide with a molecular 6 kDa, is derived from proteolysis of progranulin (PGRN). Previous study in our laboratory has shown that GRN A is able to inhibit cancer cell growth significantly. In the present study, we confirmed that GRN A can bind to α-enolase (ENO1) specifically as analyzed using Pull-down/MS approaches. The interaction of GRN A with ENO1 was further confirmed by Western blotting and Surface plasmon resonance (SPR) analysis. Treatment of human HepG-2 cells with GRN A inhibited cancer cell growth as well as migration and invasion of cancer cells as analyzed by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazoliumbromide (MTT) and Scratch wound healing assay as well as Transwell experiments. Additionally, GRN A treatment results in augmentation of glucose uptake in cancer cells. Further study reveals that higher expression of ENO1 reversed the inhibitory effects of GRN A on migration and invasion of HepG-2 cells. The increase of glucose uptake, as well as the expression of apoptosis-related genes, is also reversed in cells overexpressing ENO1. The study provides solid evidence that there is the interaction between GRN A and ENO1 and the interaction is responsible for the effects of GRN A on glucose uptake as well as cancer cell migration and invasion.

Indexed as

ApoptosisBiomarkers, TumorCarcinoma, HepatocellularCell Line, TumorCell MovementCell ProliferationDNA-Binding ProteinsGene ExpressionGlucoseGranulinsHumansIntercellular Signaling Peptides and ProteinsLiver NeoplasmsPhosphopyruvate HydrataseProtein BindingProtein Interaction MappingBiomarkers, TumorDNA-Binding ProteinsENO1 protein, humanGlucoseGranulinsIntercellular Signaling Peptides and ProteinsPhosphopyruvate HydrataseTumor Suppressor Proteinsenolase 1granulin Ainvasionmigrationprotein-protein interaction

Identifiers

PMID28415822
PMCPMC5444744
OpenAlexW2597173714

What OpenQuestion holds

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LicenceCC BY
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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.