Evidence map›Paper›PMID 25973056›Full record

ArticleInternational journal of clinical and experimental pathology2015

SOX14 promotes proliferation and invasion of cervical cancer cells through Wnt/β-catenin pathway.

Fei Li, Tairen Wang, Shengjian Tang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Clinical Significance of SOX10 Expression in Human Pathology.Current issues in molecular biology · 2023
    Review
  4. Article
  5. Development of anMolecular therapy. Methods & clinical development · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Cancer biology & medicine · 2019
    Article
  17. Wnt signaling in cervical cancer?Journal of Cancer · 2018
    Review
  18. Review
  19. Article
  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

3 authors at 1 institution in 1 country.

Fei LiHospital of Plastic Surgery, Shandong Provinicial Key Laboratory of Plastic Surgery And Microscopic Reconstructive Surgery Techniques, Weifang Medical University Weifang, Shandong Province, P.R. China.
Tairen WangHospital of Plastic Surgery, Shandong Provinicial Key Laboratory of Plastic Surgery And Microscopic Reconstructive Surgery Techniques, Weifang Medical University Weifang, Shandong Province, P.R. China.
Shengjian TangHospital of Plastic Surgery, Shandong Provinicial Key Laboratory of Plastic Surgery And Microscopic Reconstructive Surgery Techniques, Weifang Medical University Weifang, Shandong Province, P.R. China.
Weifang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SOX14 is a member of the SOXB2 subgroup of transcription factors implicated in neural development. Although SOX14 expression profile and function during development was revealed in various animal model systems, the role of this gene during tumor progression is totally unknown. In this study, the expression of SOX14 increases in four cervical cancer cell lines (HeLa, Caski, HT-3 and SiHa) as revealed by real-time PCR and Western blot analyses. Through knocking down or overexpressing SOX14 in SiHa and HeLa cells, the expression level of SOX14 was found to be positively related to cell proliferation and invasion in vitro. Moreover, the TOP-Flash reporter assay and Western blot for β-catenin genes of the Wnt/β-catenin pathway, indicated that SOX14 significantly activated Wnt/β-catenin signaling. Further study showed that the blockage of Wnt/β-catenin pathway by knocking down β-catenin resulted in a significant inhibition of cell proliferation and invasion capacity induced by SOX14. To summarize, these results demonstrate that SOX14 can promote proliferation and invasion capacity of cervical cancer cells by activating the Wnt/β-catenin pathway.

Indexed as

Blotting, WesternCell ProliferationFemaleHeLa CellsHumansNeoplasm InvasivenessReal-Time Polymerase Chain ReactionSOXB2 Transcription FactorsTransfectionUterine Cervical NeoplasmsWnt Signaling PathwaySOX14 protein, humanSOXB2 Transcription Factorscervical cancerinvasionproliferationSOX14Wnt/β-catenin pathway

Identifiers

PMID25973056
PMCPMC4396331
OpenAlexW239347600

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.