Evidence map›Paper›PMID 34713767›Full record

ArticleBioengineered2021

Linc00467 promotion of gastric cancer development by directly regulating miR-7-5p expression and downstream epidermal growth factor receptor.

Li-Hao Deng, Hui Zhao, Li-Ping Bai, Jun Xie, Kai Liu, Feng Yan

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Bioengineered, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Current issues in molecular biology · 2025
    Article
  2. Article
  3. Review
  4. Review
  5. LINC00467 mediates the 5-fluorouracil resistance in breast cancer cells.In vitro cellular & developmental biology. Animal · 2024
    Article
  6. Review
  7. LINC00467: an oncogenic long noncoding RNA.Cancer cell international · 2022
    Review
  8. Article
  9. Article
  10. 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

6 authors at 2 institutions in 1 country.

Li-Hao DengDepartment of Gastrointestinal Surgery, The Affiliated Zhongshan Hospital of Xiamen University; Institute of Gastrointestinal Oncology, Medical College of Xiamen University, Xiamen, China.
Hui ZhaoMedical Cosmetology, Xiamen Hospital of Traditional Chinese Medicine, Xiamen, China.
Li-Ping BaiDepartment of Gastrointestinal Surgery, The Affiliated Zhongshan Hospital of Xiamen University; Institute of Gastrointestinal Oncology, Medical College of Xiamen University, Xiamen, China.
Jun XieDepartment of Gastrointestinal Surgery, The Affiliated Zhongshan Hospital of Xiamen University; Institute of Gastrointestinal Oncology, Medical College of Xiamen University, Xiamen, China.
Kai LiuDepartment of Gastrointestinal Surgery, The Affiliated Zhongshan Hospital of Xiamen University; Institute of Gastrointestinal Oncology, Medical College of Xiamen University, Xiamen, China.
Feng YanDepartment of Gastrointestinal Surgery, The Affiliated Zhongshan Hospital of Xiamen University; Institute of Gastrointestinal Oncology, Medical College of Xiamen University, Xiamen, China.ORCID 0000-0002-3382-954X
Zhongshan Hospital of Xiamen University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Linc00467 is a vital regulator in tumor progression. This study explores the molecular mechanisms of linc00467 in gastric cancer (GC). Linc00467 expression was obtained and analyzed in GC tissue through exploration in the cancer genome atlas database. Then, real-time quantitative polymerase chain reaction was used to detect linc000467 expression in GC cells. Cell functions were observed using cell counting Kit-8, Transwell assay, Western blotting to testify the proliferation, migration, invasion, and the relative expression of epidermal growth factor receptor (EGFR) in GC cells. Moreover, a dual-luciferase reporter gene assay was used to verify the relationship between linc00467 and miR-7-5p. Results showed that the expression of linc00467 was overexpressed in GC. Linc00467 silencing decreased the GC cell proliferation, migration, and invasion. With mRNA verification and combined previous research, linc00467 directly regulated the miR-7-5p expression and downstream EGFR expression. Inhibited miR-7-5p could restore cell function, EGFR expression of GC cells when linc00467 knockdown occurs. Altogether, linc00467 directly regulates the miR-7-5p and EGFR signaling pathway to promote GC proliferation, migration, and invasion.

Indexed as

Gene Expression Regulation, NeoplasticCell Line, TumorErbB ReceptorsHumansMicroRNAsNeoplasm ProteinsRNA, Long NoncodingRNA, NeoplasmStomach NeoplasmsEGFR protein, humanErbB ReceptorsMicroRNAsMIRN7-1 microRNA, humanNeoplasm ProteinsRNA, Long NoncodingRNA, Neoplasmepidermal growth factor receptorGastric cancerinvasionlinc00467migrationmiR-7-5pproliferation

Identifiers

PMID34713767
PMCPMC8810099
OpenAlexW3208301186

What OpenQuestion holds

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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.