Evidence map›Paper›PMID 15471560›Full record

ArticleCancer science2004

Methylation-associated silencing of the Wnt antagonist SFRP1 gene in human ovarian cancers.

Toshio Takada, Yukiko Yagi, Takao Maekita, Masayoshi Imura, Shunsuke Nakagawa, Sai-Wah Tsao, Kazuaki Miyamoto, Osamu Yoshino, Toshiharu Yasugi, Yuji Taketani and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer science, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

  1. Wnt signaling in ovarian tumorigenesis.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
    Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Prognostic Relevance of SFRP1 Gene Promoter Methylation in Colorectal CarcinomaAsian Pacific journal of cancer prevention : APJCP · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Can we safely target the WNT pathway?Nature reviews. Drug discovery · 2014
    Review
  18. Article
  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

11 authors at 3 institutions in 4 countries.

Toshio TakadaCarcinogenesis Division, National Cancer Center Hospital, Chuo-ku, Tokyo 104-0045, Japan.
Yukiko Yagi
Takao Maekita
Masayoshi Imura
Shunsuke Nakagawa
Sai-Wah Tsao
Kazuaki Miyamoto
Osamu Yoshino
Toshiharu Yasugi
Yuji Taketani
Toshikazu Ushijima
National Cancer Center · USThe University of Tokyo · JPChinese University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SFRP1 gene on chromosome 8p11.2 encodes a Wnt signaling antagonist, and was recently demonstrated to be a new tumor suppressor that is inactivated by promoter methylation in human colon cancers. Here, we analyzed promoter methylation of the SFRP1 gene in human ovarian cancers, in which loss of heterozygosity in 8p is frequently observed and involvement of the Wnt signaling pathway has been suggested. Methylation-specific PCR (MSP) analysis showed that four of 13 ovarian cancer cell lines and two of 17 primary ovarian cancers had methylated SFRP1, while an immortalized ovarian epithelial cell line, HOSE, and seven ovarian endometrial cyst samples did not. In the four ovarian cancer cell lines with the methylation, SFRP1 was not expressed at all as determined by quantitative RT-PCR analysis. A cell line with SFRP1 methylation, MCAS, was treated with a demethylating agent, 5-aza-2'-deoxycytidine, and demethylation of the promoter and re-expression of SFRP1 were observed. These results show that SFRP1 is inactivated by promoter methylation in human ovarian cancers, as well as colon cancers.

Indexed as

DNA MethylationGene SilencingAdultAgedAzacitidineDecitabineDNA Modification MethylasesEnzyme InhibitorsFemaleGene Expression Regulation, NeoplasticHumansIntercellular Signaling Peptides and ProteinsMembrane ProteinsMiddle AgedOvarian NeoplasmsPromoter Regions, GeneticAzacitidineDecitabineDNA Modification MethylasesEnzyme InhibitorsIntercellular Signaling Peptides and ProteinsMembrane ProteinsProto-Oncogene ProteinsRNA, MessengerSecreted Frizzled-Related ProteinsSFRP1 protein, humanWnt Proteins

Identifiers

PMID15471560
PMCPMC11160044
OpenAlexW2162726435

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.