Evidence map›Paper›PMID 28553938›Full record

ArticleNature cell biology2017

The MBNL3 splicing factor promotes hepatocellular carcinoma by increasing PXN expression through the alternative splicing of lncRNA-PXN-AS1.

Ji-Hang Yuan, Xiao-Ning Liu, Tian-Tian Wang, Wei Pan, Qi-Fei Tao, Wei-Ping Zhou, Fang Wang, Shu-Han Sun

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 204 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
204citing papers in PubMed, 1 pooled it
14.7field-weighted citation impact, top 1% 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

204 citing papers in PubMed, 1 synthesis or guideline pooled it, 427 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Role of alternative splicing in cancer progression.Irish journal of medical science · 2026
    Review
  6. Review
  7. Article
  8. Review
  9. LncRNA SNHG3: a potential biomarker for human diseases.Frontiers in cell and developmental biology · 2026
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. mCancer cell international · 2025
    Article
  17. Article
  18. Review
  19. Review
  20. mCellular and molecular life sciences : CMLS · 2025
    Article

144 more citing papers are in PubMed but not listed here.

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.

Ji-Hang YuanDepartment of Medical Genetics, Second Military Medical University, Shanghai 200433, China.
Xiao-Ning LiuDepartment of Medical Genetics, Second Military Medical University, Shanghai 200433, China.
Tian-Tian WangDepartment of Medical Genetics, Second Military Medical University, Shanghai 200433, China.
Wei PanDepartment of Medical Genetics, Second Military Medical University, Shanghai 200433, China.
Qi-Fei TaoThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200433, China.
Wei-Ping ZhouThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai 200433, China.
Fang WangDepartment of Medical Genetics, Second Military Medical University, Shanghai 200433, China.
Shu-Han SunDepartment of Medical Genetics, Second Military Medical University, Shanghai 200433, China.
Second Military Medical University · CNEastern Hepatobiliary Surgery Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the roles of splicing factors and splicing events during tumorigenesis would open new avenues for targeted therapies. Here we identify an oncofetal splicing factor, MBNL3, which promotes tumorigenesis and indicates poor prognosis of hepatocellular carcinoma patients. MBNL3 knockdown almost completely abolishes hepatocellular carcinoma tumorigenesis. Transcriptomic analysis revealed that MBNL3 induces lncRNA-PXN-AS1 exon 4 inclusion. The transcript lacking exon 4 binds to coding sequences of PXN mRNA, causes dissociation of translation elongation factors from PXN mRNA, and thereby inhibits PXN mRNA translation. In contrast, the transcript containing exon 4 preferentially binds to the 3' untranslated region of PXN mRNA, protects PXN mRNA from microRNA-24-AGO2 complex-induced degradation, and thereby increases PXN expression. Through inducing exon 4 inclusion, MBNL3 upregulates PXN, which mediates the pro-tumorigenic roles of MBNL3. Collectively, these data demonstrate detailed mechanistic links between an oncofetal splicing factor, a splicing event and tumorigenesis, and establish splicing factors and splicing events as potential therapeutic targets.

Indexed as

Alternative Splicing3' Untranslated RegionsAnimalsArgonaute ProteinsBinding SitesCarcinoma, HepatocellularCarrier ProteinsCell ProliferationExonsGene Expression ProfilingGene Expression Regulation, NeoplasticHep G2 CellsHigh-Throughput Nucleotide SequencingHumansLiver NeoplasmsMale3' Untranslated RegionsAGO2 protein, humanArgonaute ProteinsCarrier ProteinsMBNL3 protein, humanMBNL3 protein, mouseMicroRNAsMIRN24 microRNA, humanNanog Homeobox ProteinNANOG protein, humanOctamer Transcription Factor-3PaxillinPOU5F1 protein, humanPXN-AS1 non-coding RNA, humanPXN protein, humanRNA-Binding ProteinsRNA, Long NoncodingSOX2 protein, humanSOXB1 Transcription Factors

Identifiers

PMID28553938
OpenAlexW2618859545

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.