Evidence map›Paper›PMID 35124606›Full record

ArticleTechnology and health care : official journal of the European Society for Engineering and Medicine2022

The role of splicing factor PRPF8 in breast cancer.

Difei Cao, Jiaying Xue, Guoqing Huang, Jing An, Weiwei An

Open access · bronzeAbstract read
In one paragraph

Article in Technology and health care : official journal of the European Society for Engineering and Medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Research Progress on the Relationship Between PRPF8 and Cancer.Current issues in molecular biology · 2025
    Review
  3. A de novoHormone research in paediatrics · 2025
    Article
  4. Article
  5. Non-Coding RNAs in Breast Cancer: Diagnostic and Therapeutic Implications.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. 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

5 authors at 1 institution in 1 country.

Difei CaoInstitute of Advanced Technology, Heilongjiang Academy of Sciences, Harbin, Heilongjiang, China.
Jiaying XueInstitute of Advanced Technology, Heilongjiang Academy of Sciences, Harbin, Heilongjiang, China.
Guoqing HuangInstitute of Advanced Technology, Heilongjiang Academy of Sciences, Harbin, Heilongjiang, China.
Jing AnInstitute of Cancer Prevention and Treatment, Heilongjiang Province Academy of Medical Sciences, Harbin, Heilongjiang, China.
Weiwei AnInstitute of Cancer Prevention and Treatment, Heilongjiang Province Academy of Medical Sciences, Harbin, Heilongjiang, China.
Heilongjiang Academy of Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlternative splicing is a mechanism to produce different proteins with diverse functions from one gene. Many splicing factors play an important role in cancer progression. PRPF8 is a core protein component of the spliceosome complex, U4/U6-U5 tri-snRNP.

objectiveHowever, PRPF8 involved in mRNA alternative splicing are rarely included in the prognosis.

methodsWe found that PRPF8 was expressed in all examined cancer types. Further analyses found that PRPF8 expression was significantly different between the breast cancer and paracancerous tissues.

resultsSurvival analyses showed that PRPF8-high patients had a poor prognosis, and the expression of PRPF8 is associated with distant metastasis-free survival (DMFS) and post progression survival (PPS). Gene Set Enrichment Analysis (GSEA) has revealed that PRPF8 expression is correlated with TGF-β, JAK-STAT, and cell cycle control pathways. Consistent with these results, upon PRPF8 silencing, the growth of MCF-7 cells was reduced, the ability of cell clone formation was weakened, and p⁢21 expression was increased.

conclusionsThese results have revealed that PRPF8 is a significant factor for splicing in breast cancer progression.

Indexed as

Breast NeoplasmsRibonucleoprotein, U5 Small NuclearFemaleHeLa CellsHumansRibonucleoprotein, U4-U6 Small NuclearRNA-Binding ProteinsRNA Splicing FactorsPRPF8 protein, humanRibonucleoprotein, U4-U6 Small NuclearRibonucleoprotein, U5 Small NuclearRNA-Binding ProteinsRNA Splicing Factorsalternative splicingbreast cancerprognosisPRPF8

Identifiers

PMID35124606
PMCPMC9051661
OpenAlexW4210303536

What OpenQuestion holds

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Registered trials

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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.