Evidence map›Paper›PMID 26336992›Full record

ArticleOncotarget2015

Regulation and functional significance of CDC42 alternative splicing in ovarian cancer.

Xiaolong He, Chengfu Yuan, Jilai Yang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. PTBP1 and Cancer: From RNA Regulation to Therapeutic Potential.Journal of cellular and molecular medicine · 2025
    Review
  3. Review
  4. Alternative splicing in ovarian cancer.Cell communication and signaling : CCS · 2024
    Review
  5. Review
  6. Downregulation of Splicing FactorCurrent issues in molecular biology · 2024
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Targeting Cancer by Using Nanoparticles to Modulate RHO GTPase Signaling.Advances in experimental medicine and biology · 2022
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 3 institutions in 2 countries.

Xiaolong HeDepartment of Biopharmaceutical Sciences, College of Pharmacy-Rockford, The University of Illinois at Chicago, Rockford, IL 61107, USA.
Chengfu YuanMedical College of China Three Gorges University, Yichang, Hubei, 443002, People's Republic of China.
Jilai YangDepartment of Biopharmaceutical Sciences, College of Pharmacy-Rockford, The University of Illinois at Chicago, Rockford, IL 61107, USA.
China Three Gorges University · CNUniversity of Illinois Chicago · USUniversity of Illinois Chicago, Rockford campus · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our previous study found that splicing factor polypyrimidine tract-binding protein 1 (PTBP1) had a role in tumorigenesis but the underlying mechanism remained unclear. In this study, we observed that knockdown of PTBP1 inhibited filopodia formation. Subsequently, we found that PTBP1 regulated the alternative splicing of CDC42, a major regulator of filopodia formation. Two CDC42 variants, CDC42-v1 and CDC42-v2, can be generated through alternative splicing. Knockdown of PTBP1 increased the expression of CDC42-v2. Ectopic expression of individual variants showed that CDC42-v2 suppressed filopodia formation, opposite to the effect of CDC42-v1. Quantitative RT-PCR revealed that CDC42-v2 was expressed at lower levels in ovarian cancer cell lines and ovarian tumor tissues than in normal control cells and tissues. Further, CDC42-v2 was observed to have inhibitory effects on ovarian tumor cell growth, colony formation in soft agar and invasiveness. In contrast, these inhibitory effects were not found with CDC42-v1. Taken together, above results suggest that the role of PTBP1 in tumorigenesis may be partly mediated by its regulation of CDC42 alternative splicing and CDC42-v2 might function as a tumor suppressor.

Indexed as

Alternative SplicingGene Expression Regulation, NeoplasticAnimalsBase SequenceBlotting, Westerncdc42 GTP-Binding ProteinCell Line, TumorCell ProliferationFemaleHEK293 CellsHeterogeneous-Nuclear RibonucleoproteinsHumansMiceMolecular Sequence DataNIH 3T3 CellsOvarian Neoplasmscdc42 GTP-Binding ProteinHeterogeneous-Nuclear RibonucleoproteinsPolypyrimidine Tract-Binding ProteinProtein IsoformsPTBP1 protein, humanalternative splicingCDC42ovarian cancerPTBP1

Identifiers

PMID26336992
PMCPMC4745753
OpenAlexW1845295852

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.