Evidence map›Paper›PMID 33251387›Full record

ArticleNon-coding RNA research2020

MicroRNA-7-5p's role in the O-GlcNAcylation and cancer metabolism.

Sin Yung Woo, Su Yel Lee, Seong-Lan Yu, Se Jin Park, Daeun Kang, Jin Suk Kim, In Beom Jeong, Sun Jung Kwon, Wan Jin Hwang, Chang Ryul Park and 1 more

Open access · goldAbstract read
In one paragraph

Article in Non-coding RNA research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. CanPharmaceuticals (Basel, Switzerland) · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. A nexus of lipid andFrontiers in endocrinology · 2022
    Review
  10. Metabolic Control by DNA Tumor Virus-Encoded Proteins.Pathogens (Basel, Switzerland) · 2021
    Review
  11. MiR-7 in Cancer Development.Biomedicines · 2021
    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 4 institutions in 1 country.

Sin Yung WooDepartment of Internal Medicine, Konyang University Hospital, South Korea.
Su Yel LeePriority Research Center, Myunggok Research Institute, College of Medicine, Konyang University, South Korea.
Seong-Lan YuPriority Research Center, Myunggok Research Institute, College of Medicine, Konyang University, South Korea.
Se Jin ParkDepartment of Internal Medicine, Konyang University Hospital, South Korea.
Daeun KangDepartment of Internal Medicine, Konyang University Hospital, South Korea.
Jin Suk KimDepartment of Nuclear Medicine, Konyang University Hospital, South Korea.
In Beom JeongDepartment of Internal Medicine, Konyang University Hospital, South Korea.
Sun Jung KwonDepartment of Internal Medicine, Konyang University Hospital, South Korea.
Wan Jin HwangDepartment of Thoracic and Cardiovascular Surgery, Seoul National University Bundang Hospital, South Korea.
Chang Ryul ParkUlsan University Hospital, University of Ulsan College of Medicine, South Korea.
Ji Woong SonDepartment of Internal Medicine, Konyang University Hospital, South Korea.
Konyang University Hospital · KRKonyang University · KRSeoul National University Bundang Hospital · KRUlsan College · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

O-GlcNAc Transferase (OGT) is a complementary enzyme that regulates O-linked N-acetylglucosaminylation(O-GlcNAcylation) and plays a critical role in various cancer phenotypes, including invasion, migration, and metabolic reprogramming. In our previous study we found that miR-7-5p was downregulated at lung cancer cells with highly metastatic capacity. In the in-silico approach, OGT is the predicted target of miR-7-5p. To identify miR-7-5p's role in cell growth and metabolism, we transfected various lung cancer cell lines with miR-7-5p. The expression level of miR-7-5p was confirmed by qRT-PCR in lung cancer cell lines. Western blot assays and qRT-PCR were performed to demonstrate miR-7-5p's effect. Bioinformatic analysis indicated that OGT is a direct target of miR-7-5p. The binding sites of miR-7-5p in the OGT 3' UTR were verified by luciferase reporter assay. To investigate the role of miR-7-5p in the cancer metabolism of non-small cell lung cancer (NSCLC) cells, mimic of miR-7-5p was transfected into NSCLC cells, and the effect of miR-7-5p on cancer metabolism was analyzed by LDH assays, glucose uptake, and mitochondrial ATP synthase inhibitor assay. O-GlcNAcylated protein level was determined by Western blot. The role of miR-7-5p in lung cancer growth was measured by MTS assays. To identify the delivery of miR-7-5p via PLGA, an

Indexed as

anaerobic GlycolysisCancer metabolismGlycosylationLung cancermicroRNAOGTPLGA

Identifiers

PMID33251387
PMCPMC7677666
OpenAlexW3101751005

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.