Evidence map›Paper›PMID 29371697›Full record

ArticleExperimental & molecular medicine2018

RNF138-mediated ubiquitination of rpS3 is required for resistance of glioblastoma cells to radiation-induced apoptosis.

Wanyeon Kim, HyeSook Youn, Sungmin Lee, EunGi Kim, Daehoon Kim, Jung Sub Lee, Jae-Myung Lee, BuHyun Youn

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

42 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. PELI1: key players in the oncogenic characteristics of pancreatic Cancer.Journal of experimental & clinical cancer research : CR · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  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

8 authors at 2 institutions in 1 country.

Wanyeon KimDepartment of Biological Sciences, Pusan National University, Busan, Republic of Korea.
HyeSook YounDepartment of Integrative Bioscience and Biotechnology, Sejong University, Seoul, Republic of Korea.
Sungmin LeeDepartment of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
EunGi KimDepartment of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
Daehoon KimDepartment of Integrated Biological Science, Pusan National University, Busan, Republic of Korea.
Jung Sub LeeDepartment of Orthopaedic Surgery, Medical Research Institute, Pusan National University School of Medicine, Busan, Republic of Korea.
Jae-Myung LeeDepartment of Naval Architecture and Ocean Engineering, Pusan National University, Busan, Republic of Korea.
BuHyun YounDepartment of Biological Sciences, Pusan National University, Busan, Republic of Korea.
Pusan National University · KRSejong University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An interaction between ribosomal protein S3 (rpS3) and nuclear factor kappa B or macrophage migration inhibitory factor in non-small-cell lung cancer is responsible for radioresistance. However, the role of rpS3 in glioblastoma (GBM) has not been investigated to date. Here we found that in irradiated GBM cells, rpS3 translocated into the nucleus and was subsequently ubiquitinated by ring finger protein 138 (RNF138). Ubiquitin-dependent degradation of rpS3 consequently led to radioresistance in GBM cells. To elucidate the apoptotic role of rpS3, we analyzed the interactome of rpS3 in ΔRNF138 GBM cells. Nuclear rpS3 interacted with DNA damage inducible transcript 3 (DDIT3), leading to DDIT3-induced apoptosis in irradiated ΔRNF138 GBM cells. These results were confirmed using in vivo orthotopic xenograft models and GBM patient tissues. This study aims to clarify the role of RNF138 in GBM cells and demonstrate that rpS3 may be a promising substrate of RNF138 for the induction of GBM radioresistance, indicating RNF138 as a potential target for GBM therapy.

Indexed as

AdultAgedAnimalsApoptosisBrain NeoplasmsCell Line, TumorFemaleGlioblastomaHumansMaleMice, Inbred BALB CMiddle AgedProtein Phosphatase 1Radiation, IonizingRadiation ToleranceRibosomal ProteinsDDIT3 protein, humanPPP1R15A protein, humanProtein Phosphatase 1Ribosomal ProteinsRNF138 protein, humanRPS3 protein, humanTranscription Factor CHOPUbiquitin-Protein Ligases

Identifiers

PMID29371697
PMCPMC5799804
OpenAlexW2784694452

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.