Evidence map›Paper›PMID 29100356›Full record

ArticleOncotarget2017

PAX2 maintains the differentiation of mouse oviductal epithelium and inhibits the transition to a stem cell-like state.

Kholoud Alwosaibai, Atefeh Abedini, Ensaf M Al-Hujaily, Yong Tang, Kenneth Garson, Olga Collins, Barbara C Vanderhyden

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Loss ofOncotarget · 2025
    Article
  4. Clinical implications of epithelial-to-mesenchymal transition in cancers which potentially spread to peritoneum.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  5. Review
  6. Decoding Müllerian Duct Epithelial Regionalization.Molecular reproduction and development · 2025
    Review
  7. Loss of phosphatase and tensin homolog (Cancer pathogenesis and therapy · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Gain-of-function p53Scientific reports · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Metalloproteinases in Ovarian Cancer.International journal of molecular sciences · 2021
    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

7 authors at 5 institutions in 3 countries.

Kholoud AlwosaibaiDepartment of Cellular and Molecular Medicine, University of Ottawa, Ontario, Canada.
Atefeh AbediniDepartment of Cellular and Molecular Medicine, University of Ottawa, Ontario, Canada.
Ensaf M Al-HujailyDepartment of Cellular and Molecular Medicine, University of Ottawa, Ontario, Canada.
Yong TangDepartment of Urology, Affiliated Cancer Hospital of Guangxi Medical University, Nanning, China.
Kenneth GarsonDepartment of Cellular and Molecular Medicine, University of Ottawa, Ontario, Canada.
Olga CollinsDepartment of Cellular and Molecular Medicine, University of Ottawa, Ontario, Canada.
Barbara C VanderhydenDepartment of Cellular and Molecular Medicine, University of Ottawa, Ontario, Canada.
Ottawa Hospital Research InstituteUniversity of Ottawa · CAGuangxi Medical University · CNKing Fahad Specialist Hospital · SAOttawa Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have provided evidence that the secretory cells of the fallopian tube (oviduct) are a probable origin for high-grade serous ovarian carcinoma. In addition to secretory cells, the fallopian tube epithelium consists of ciliated cells and CD44+ undifferentiated stem-like cells. Loss of PAX2 expression is recognized as an early event in epithelial transformation, but the specific role of PAX2 in this transition is unknown. The aim of this study was to define the role of PAX2 in oviductal epithelial (OVE) cells and its response to transforming growth factor β1 (TGFβ), characterizing specifically its potential involvement in regulating stem cell-like behaviors that may contribute to formation of cancer-initiating cells. Treatment of primary cultures of mouse OVE cells with TGFβ induced an epithelial-mesenchymal transition (EMT) associated with decreased expression of PAX2 and an increase in the fraction of cells expressing CD44. PAX2 knockdown in OVE cells and overexpression in ovarian epithelial cells confirmed that PAX2 inhibits stem cell characteristics and regulates the degree of epithelial differentiation of OVE cells. These results suggest that loss of PAX2, as occurs in serous tubal intraepithelial carcinomas, may shift secretory cells to a more mesenchymal phenotype associated with stem-like features.

Indexed as

epithelial-mesenchymal transitionfallopian tubeovarian cancerPAX2stem cells

Identifiers

PMID29100356
PMCPMC5652750
OpenAlexW2604787987

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.