Evidence map›Paper›PMID 31754130›Full record

ArticleScientific reports2019

Regulation of carcinogenesis and modulation through Wnt/β-catenin signaling by curcumin in an ovarian cancer cell line.

Hsing-Yu Yen, Chih-Wei Tsao, Ya-Wen Lin, Chih-Chi Kuo, Chang-Huei Tsao, Chin-Yu Liu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

36 citing papers in PubMed, 64 citations in OpenAlex.

  1. The role of cytokines in ovarian cancer drug resistance.International journal of cancer · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. The role of curcumin in modulating circular RNAs and long non-coding RNAs in cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Wnt antagonist as therapeutic targets in ovarian cancer.The international journal of biochemistry & cell biology · 2022
    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

6 authors at 4 institutions in 1 country.

Hsing-Yu YenDepartment of Nutritional Science, Fu Jen Catholic University, Taipei, Taiwan.
Chih-Wei TsaoDivision of Urology, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Ya-Wen LinDepartment of Microbiology and Immunology, National Defense Medical Centre, Taipei, Taiwan.
Chih-Chi KuoTeaching and Research Office, Tri-Service General Hospital Songshan Branch, Taipei, Taiwan.
Chang-Huei TsaoDepartment of Microbiology and Immunology, National Defense Medical Centre, Taipei, Taiwan.
Chin-Yu LiuDepartment of Nutritional Science, Fu Jen Catholic University, Taipei, Taiwan. nf351.lab@gmail.com.
Fu Jen Catholic University · TWNational Defense Medical Center · TWTri-Service General Hospital · TWTri-Service General Hospital Songshan Branch · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The secreted frizzled-related protein 5 gene (SFRP5) that antagonize the Wnt/β-catenin signaling is frequently inactivated by promoter methylation and oncogenic activation of the Wnt signaling pathway is common in many cancers. The curcumin-rich Curcuma longa has been reported to potent anti-cancer property involved in epigenetic regulation to inhibit tumor suppressor gene methylation and re-expression. In a compounds screening, we found that curcumin can inhibit Wnt/β-catenin signaling. Therefore, the aim of this study was to investigate the effects of curcumin on SFRP5 DNA methylation modification in an ovarian cancer cell line (SKOV3). SKOV3 cells were treated with DMSO, 10 μM 5-aza-2'-deoxycytidine (DAC), 5 μM DAC, 20 μM curcumin, and 20 μM curcumin combined with 5 μM DAC for 96 hours, following which RNA and proteins were extracted for further analysis. The results showed that curcumin combined with 5 μM DAC may inhibit cancer cell colony formation, migration through EMT (epithelial-mesenchymal transition) process regulation, total DNMT activity, especially in DNMT3a protein expression, and may also regulate tumor suppressor gene SFRP5 expression involved in the Wnt/β-catenin signaling pathway. The combined treatment attenuated ovarian cancer development.

Indexed as

Adaptor Proteins, Signal Transducingbeta CateninCarcinogenesisCell Line, TumorCell ProliferationCurcuminDNA MethylationDNA Modification MethylasesEpigenesis, GeneticEpigenomicsEpithelial-Mesenchymal TransitionFemaleHumansOvarian NeoplasmsPromoter Regions, GeneticSecreted Frizzled-Related ProteinsAdaptor Proteins, Signal Transducingbeta CateninCurcuminDNA Modification MethylasesSecreted Frizzled-Related ProteinsSFRP5 protein, human

Identifiers

PMID31754130
PMCPMC6872918
OpenAlexW2989722486

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.