Evidence map›Paper›PMID 23056560›Full record

ArticlePloS one2012

Alterations of the WNT7A gene in clear cell renal cell carcinomas.

Aleksandr G Kondratov, Sergiy M Kvasha, Liubov A Stoliar, Alina M Romanenko, Yury M Zgonnyk, Vasily V Gordiyuk, Elena V Kashuba, Alla V Rynditch, Eugene R Zabarovsky, Vladimir I Kashuba

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. 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
1.1field-weighted citation impact, top 25% 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, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Mechanistic Insights into Tumorigenesis from Serum Proteins.medRxiv : the preprint server for health sciences · 2025
    Article
  4. Review
  5. Review
  6. Review
  7. New insights into fibrotic signaling in renal cell carcinoma.Frontiers in cell and developmental biology · 2023
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Wnt Signaling in Kidney Development and Disease.Progress in molecular biology and translational science · 2018
    Review
  16. Loss of Wnt7a expression correlates with tumor progression and poor prognosis in colorectal carcinoma.International journal of clinical and experimental pathology · 2018
    Article
  17. Inhibition of WNT7A-β-catenin signaling pathway sensitizes oral squamous cell carcinoma to cisplatin.International journal of clinical and experimental pathology · 2018
    Article
  18. Wnt signaling in cervical cancer?Journal of Cancer · 2018
    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

10 authors at 4 institutions in 3 countries.

Aleksandr G KondratovDepartment of Molecular Oncogenetics, Institute of Molecular Biology and Genetics, National Academy of Science, Kyiv, Ukraine. o.g.kondratov@imbg.org.ua
Sergiy M Kvasha
Liubov A Stoliar
Alina M Romanenko
Yury M Zgonnyk
Vasily V Gordiyuk
Elena V Kashuba
Alla V Rynditch
Eugene R Zabarovsky
Vladimir I Kashuba
Institute of Molecular Biology and Genetics · UAInstitute of Urology of the National Academy of Medical Sciences of Ukraine · UAEngelhardt Institute of Molecular Biology · RUKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

WNT7A (wingless-type MMTV integration site family, member 7A) is a known tumor suppressor gene of non-small cell lung carcinomas (NSCLC) and is frequently inactivated due to CpG-island hypermethylation in human cancers. The members of WNT family are involved in cell signaling and play crucial roles in cancer development. In the present work hypermethylation of the WNT7A gene was detected in 66% (29/44) of analyzed clear cell renal cell carcinomas (RCCs) using methyl-specific PCR (MSP). Moreover, bisulfite sequencing confirmed intensive hypermethylation of the 5'-CpG island of the WNT7A gene. Methylation analysis revealed positive correlations between tumor stage, Fuhrman nuclear grade and WNT7A hypermethylation. Additionally, restoration of WNT7A gene expression in the A498 cell line by 5-aza-2'-deoxycytidine treatment confirmed a direct contribution of hypermethylation in silencing of the WNT7A gene. High frequency of loss of heterozygosity (LOH) was demonstrated on chromosome 3p25 in regions surrounding the WNT7A gene. The frequent down-regulation of WNT7A gene expression was detected in 88% (15/17) of clear cell RCCs. We have also shown that the WNT7A gene possesses tumor suppression function by colony-formation and cell proliferation assays in RCC cell lines. In summary, the WNT7A gene is inactivated by genetic/epigenetic alterations in clear cell RCC and demonstrates tumor suppressor properties.

Indexed as

AdultAgedAzacitidineCarcinoma, Renal CellCell Line, TumorCell ProliferationDecitabineDNA MethylationDown-RegulationEpigenesis, GeneticFemaleGenetic MarkersHumansLoss of HeterozygosityMaleMicrosatellite RepeatsAzacitidineDecitabineGenetic MarkersWNT7A protein, humanWnt Proteins

Identifiers

PMID23056560
PMCPMC3466251
OpenAlexW1997207036

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Registered trials

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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.