Evidence map›Paper›PMID 27524417›Full record

ArticleOncogene2017

miR-100 antagonism triggers apoptosis by inhibiting ubiquitination-mediated p53 degradation.

G Yang, Y Gong, Q Wang, L Wang, X Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2017. 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
2.5field-weighted citation impact, top 12% 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, 44 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. The TP53-activated E3 ligase RNF144B is a tumour suppressor that prevents genomic instability.Journal of experimental & clinical cancer research : CR · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Noncoding RNAs in apoptosis: identification and function.Turkish journal of biology = Turk biyoloji dergisi · 2022
    Review
  11. Article
  12. Review
  13. Review
  14. Regulating tumor suppressor genes: post-translational modifications.Signal transduction and targeted therapy · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Essential Roles of E3 Ubiquitin Ligases in p53 Regulation.International journal of molecular sciences · 2017
    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

5 authors at 2 institutions in 1 country.

G YangCollaborative Innovation Center of Deep Sea Biology and College of Life Sciences, Zhejiang University, Hangzhou, The People's Republic of China.
Y GongCollaborative Innovation Center of Deep Sea Biology and College of Life Sciences, Zhejiang University, Hangzhou, The People's Republic of China.
Q WangDepartment of Gastroenterology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, The People's Republic of China.
L WangDepartment of Gastroenterology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, The People's Republic of China.
X ZhangCollaborative Innovation Center of Deep Sea Biology and College of Life Sciences, Zhejiang University, Hangzhou, The People's Republic of China.
Zhejiang University · CNFirst Affiliated Hospital of Bengbu Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During tumourigenesis, p53 functions as 'the guardian of the genome' because p53-dependent apoptosis strongly regulates the fate of cancer cells. Therefore, p53 regulation must be sensitive and accurate. p53 activity is regulated through its ubiquitination and deubiquitination. However, the role of microRNA in ubiquitin-mediated p53 degradation has not been previously studied. Our previous studies indicated that miR-100 is required for apoptosis. In the current study, the mechanism of p53 protein ubiquitination mediated by miR-100 was characterized. An analysis of primary tumour samples from gastric cancer patients showed a significant correlation between miR-100 upregulation and primary human gastric tumourigenesis and progression. The in vivo and in vitro data indicated that miR-100 antagonism specifically induced the apoptosis of poorly differentiated gastric cancer cells but not non-cancerous gastric cells, indicating that miR-100 has a crucial role in regulating the progression of gastric tumours. In the regulation of p53-dependent apoptosis, miR-100 antagonism inhibited ubiquitin-mediated p53 protein degradation by activating RNF144B, an E3 ubiquitination ligase. Consequently, the miR-100-RNF144B-pirh2-p53-dependent pathway was initiated. Our findings highlight a novel mechanism of ubiquitin-mediated p53 protein degradation in apoptosis.

Indexed as

AnimalsApoptosisBiomarkers, TumorCell ProliferationFemaleHumansMiceMice, Inbred NODMice, SCIDMicroRNAsNeoplasm StagingPrognosisProteolysisProto-Oncogene Proteins c-mdm2Signal TransductionStomach NeoplasmsBiomarkers, TumorMicroRNAsMIRN100 microRNA, humanProto-Oncogene Proteins c-mdm2RNF144B protein, humanTP53 protein, humanTumor Suppressor Protein p53UbiquitinUbiquitin-Protein Ligases

Identifiers

PMID27524417
OpenAlexW2516250080

What OpenQuestion holds

Textmetadata
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.