Evidence map›Paper›PMID 14614460›Full record

ArticleOncogene2003

Alterations in the common fragile site gene Parkin in ovarian and other cancers.

Stacy R Denison, Fang Wang, Nicole A Becker, Birgitt Schüle, Norman Kock, Leslie A Phillips, Christine Klein, David I Smith

Abstract read
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In one paragraph

Article in Oncogene, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed
–field-weighted citation impact
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

122 citing papers in PubMed.

  1. Article
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  6. MTFR1L is a cardiac antiaging factor for maintenance of mitochondrial homeostasis.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  12. Review
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  19. Article
  20. The mitophagy pathway and its implications in human diseases.Signal transduction and targeted therapy · 2023
    Review

62 more citing papers are in PubMed but not listed here.

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

8 authors.

Stacy R DenisonDepartment of Laboratory Medicine and Pathology, Division of Experimental Pathology, Mayo Clinic Cancer Center, Mayo Foundation, 200 First Street SW, Rochester, MN 55905, USA.
Fang Wang
Nicole A Becker
Birgitt Schüle
Norman Kock
Leslie A Phillips
Christine Klein
David I Smith

Funding

CHROMOSOME BREAKPOINTS, RENAL &SMALL CELL LUNG CANCERR01CA048031 · NCI · WAYNE STATE UNIVERSITY · PI SMITH, DAVID I · 1988 to 2000
$283k
NCI NIH HHS CA48031
6 · The paper itself

Abstract

The cloning and characterization of the common fragile site (CFS) FRA6E (6q26) identified Parkin, the gene involved in the pathogenesis of many cases of juvenile, early-onset and, rarely, late-onset Parkinson's disease, as the third large gene to be localized within a large CFS. Initial analyses of Parkin indicated that in addition to playing a role in Parkinson's disease, it might also be involved in the development and/or progression of ovarian cancer. These analyses also indicated striking similarities among the large CFS-locus genes: fragile histidine triad gene (FHIT; 3p14.2), WW domain-containing oxidoreductase gene (WWOX; 16q23), and Parkin (6q26). Analyses of FHIT and WWOX in a variety of different cancer types have identified the presence of alternative transcripts with whole exon deletions. Interestingly, various whole exon duplications and deletions have been identified for Parkin in juvenile and early-onset Parkinson's patients. Therefore, we performed mutational/exon rearrangement analysis of Parkin in ovarian cancer cell lines and primary tumors. Four (66.7%) cell lines and four (18.2%) primary tumors were identified as being heterozygous for the duplication or deletion of a Parkin exon. Additionally, three of 23 (13.0%) nonovarian tumor-derived cell lines were also identified as having a duplication or deletion of one or more Parkin exons. Analysis of Parkin protein expression with antibodies revealed that most of the ovarian cancer cell lines and primary tumors had diminished or absent Parkin expression. While functional analyses have not yet been performed for Parkin, these data suggest that like FHIT and WWOX, Parkin may represent a tumor suppressor gene.

Indexed as

Alternative SplicingBase SequenceBlotting, WesternDNA PrimersFemaleGene DeletionGene DuplicationHomozygoteHumansIn Situ Hybridization, FluorescenceOvarian NeoplasmsRNA, MessengerUbiquitin-Protein LigasesDNA Primersparkin proteinRNA, MessengerUbiquitin-Protein Ligases

Identifiers

PMID14614460

What OpenQuestion holds

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Read underepoch 390

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.