Evidence map›Paper›PMID 32774161›Full record

ArticleCancer cell international2020

LncRNA TRG-AS1 stimulates hepatocellular carcinoma progression by sponging miR-4500 to modulate BACH1.

Xuehu Sun, Yeben Qian, Xingyu Wang, Rongge Cao, Jianlin Zhang, Weidong Chen, Maoyong Fang

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  4. Review
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  8. Making Sense of Antisense lncRNAs in Hepatocellular Carcinoma.International journal of molecular sciences · 2023
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Non-coding RNA in cancer.Essays in biochemistry · 2021
    Review
  15. Article
  16. Article
  17. Article
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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

7 authors at 2 institutions in 1 country.

Xuehu SunDepartment of Emergency Surgery, the First Affiliated Hospital of Anhui Medical University, Hefei, 230000 Anhui China.
Yeben QianDepartment of Hepatobiliary Surgery, the First Affiliated Hospital of Anhui Medical University, No.218 Jixi Road, Hefei, 230000 Anhui China.ORCID 0000-0002-6338-3403
Xingyu WangDepartment of Emergency Surgery, the First Affiliated Hospital of Anhui Medical University, Hefei, 230000 Anhui China.
Rongge CaoDepartment of Emergency, the First Affiliated Hospital of University of Science and Technology of China, Hefei, 230001 Anhui China.
Jianlin ZhangDepartment of Emergency Surgery, the First Affiliated Hospital of Anhui Medical University, Hefei, 230000 Anhui China.
Weidong ChenDepartment of Emergency Surgery, the First Affiliated Hospital of Anhui Medical University, Hefei, 230000 Anhui China.
Maoyong FangDepartment of Emergency Surgery, the First Affiliated Hospital of Anhui Medical University, Hefei, 230000 Anhui China.
Anhui Medical University · CNUniversity of Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundT cell receptor gamma locus antisense RNA 1 (TRG-AS1) has been reported to involve in the progression of glioblastoma, however the role and its underlying molecular mechanism in hepatocellular carcinoma (HCC) remain unknown.

methodsQuantitative real-time polymerase chain reaction (RT-qPCR) was applied to detect TRG-AS1 expression in HCC cells. Besides, the proliferation abilities of HCC cells were assessed by colony formation and EdU assays. The migratory and invasive abilities of HCC cells were examined by transwell assays. Imunofluorescence staining (IF) was used to analyze the epithelial-mesenchymal transitions (EMT). The interaction among TRG-AS1, miR-4500 and BTB domain and CNC homolog 1 (BACH1) were proofed by means of RIP and RNA pull down and luciferase reporter assays.

resultsTRG-AS1 was conspicuously overexpressed in HCC cells. TRG-AS1 silencing apparently suppressed HCC cell proliferation, migration, invasion and epithelial-mesenchymal transition (EMT). Mechanism exploration revealed that TRG-AS1 acted as a molecular sponge of miR-4500 to regulate BACH1. MiR-4500 silencing or BACH1 overexpression in BACH1-downregulated cells fully rescued cell proliferation migration, invasion and EMT progress.

conclusionTRG-AS1 regulates HCC progression by targeting miR-4500/BACH1 axis.

Indexed as

BACH1HCCmiR-4500TRG-AS1

Identifiers

PMID32774161
PMCPMC7401190
OpenAlexW3047463702

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.