Evidence map›Paper›PMID 29383172›Full record

ArticleOncotarget2017

Novel prognostic marker PRMT1 regulates cell growth via downregulation of CDKN1A in HCC.

Jea-Woon Ryu, Seon-Kyu Kim, Mi-Young Son, Su-Jin Jeon, Jung-Hwa Oh, Jung Hwa Lim, Sunwha Cho, Cho-Rok Jung, Ryuji Hamamoto, Dae-Soo Kim 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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.1field-weighted citation impact, top 22% 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, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. The Emerging Role of Stress Granules in Hepatocellular Carcinoma.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Critical Roles ofBiomolecules · 2020
    Review
  16. Review
  17. Epigenetic Alterations of Heat Shock Proteins (HSPs) in Cancer.International journal of molecular sciences · 2019
    Review
  18. Article
  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 3 institutions in 1 country.

Jea-Woon RyuKorea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Seon-Kyu KimKorea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Mi-Young SonKorea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Su-Jin JeonKorea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Jung-Hwa OhKorea Institute of Toxicology(KIT), Daejeon, Republic of Korea.
Jung Hwa LimKorea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Sunwha ChoKorea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Cho-Rok JungKorea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Ryuji HamamotoDivision of Molecular Modification and Cancer Biology, National Cancer Center, Tokyo, Japan.
Dae-Soo KimKorea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Hyun-Soo ChoKorea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
Korea Research Institute of Bioscience and Biotechnology · KRKorea University of Science and Technology · KRKorea Institute of Toxicology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a major type of liver cancer caused by the hepatitis B and C viruses, alcohol and exposure to aflatoxin. For HCC treatment, anticancer drugs have been widely used, but drug resistance in advanced HCC is an important problem, resulting in a continuous need for novel therapeutic targets. Therefore, in this study, we established a screening pipeline based on RNA-seq to screen novel therapeutic/prognostic targets in HCC and identified PRMT1 (Protein Arginine Methyltransferase 1). In the prognostic analysis, the overexpression of PRMT1 was clearly associated with poor prognosis in a number of HCC patient cohorts. Moreover, after PRMT1 knockdown, HCC cell lines exhibited cell growth and spheroid formation suppression, an increase in Sub-G1 cells by FACS analysis, and enrichment of the cell cycle pathway via functional enrichment analysis. With these results, we demonstrated that PRMT1 could be a novel prognostic marker and therapeutic target for HCC therapy.

Indexed as

HCCPRMT1prognostic marker

Identifiers

PMID29383172
PMCPMC5777784
OpenAlexW2775236373

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.