Evidence map›Paper›PMID 23748877›Full record

ArticleVirchows Archiv : an international journal of pathology2013

p53 mutations may be involved in malignant transformation of giant cell tumor of bone through interaction with GPX1.

Taketo Okubo, Tsuyoshi Saito, Hiroyuki Mitomi, Tatsuya Takagi, Tomoaki Torigoe, Yoshiyuki Suehara, Kazuo Kaneko, Takashi Yao

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 44 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Molecular and clinicopathological features of appendiceal mucinous neoplasms.Virchows Archiv : an international journal of pathology · 2021
    Article
  10. Article
  11. Histopathology of Parasellar Neoplasms.Neuroendocrinology · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. Comprehensive Analysis of Long Noncoding RNAs and Messenger RNAs Expression Profiles in Patients with Marjolin Ulcer.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Histological Regression of Giant Cell Tumor of Bone Following RANK Ligand Inhibition.Journal of investigative medicine high impact case reports
    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

8 authors at 1 institution in 1 country.

Taketo OkuboDepartment of Human Pathology, Juntendo University School of Medicine, Hongo 2-1-1, Bunkyo-ku, Tokyo, Japan.
Tsuyoshi Saito
Hiroyuki Mitomi
Tatsuya Takagi
Tomoaki Torigoe
Yoshiyuki Suehara
Kazuo Kaneko
Takashi Yao
Juntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Giant cell tumor of bone (GCTB) is a benign tumor with a tendency for local recurrence. Secondary malignant GCTB is rare, occurring in less than 2 % of GCTB cases. Mechanisms of malignant transformation of GCTB remain unclear. We examined 43 cases of GCTB (38 conventional cases, two lung implantation cases, and three secondary malignant cases) for p53 gene mutations and for loss of heterozygosity (LOH) of p53 when corresponding normal tissue was available. In addition, to elucidate the possible involvement of p53, GPX-1, cyclinD1, and Ki-67 in malignant transformation of GCTB, we assessed the expression of these proteins by immunohistochemistry. Mutations or LOH of p53 were found in all three malignant cases, which also showed p53 overexpression. Non-synonymous p53 mutations were detected in seven of 38 conventional cases (18 %), although none of these showed p53 overexpression, defined as more than 10 % of cells being positive. LOH at the p53 locus was detected in eight of 37 informative cases, although this was not associated with p53 overexpression in conventional GCT. Expression of GPX-1 was higher in the recurrent group, which included metastatic and malignant cases, and patients with high GPX-1 expression were at greater risk for early relapse. We also observed a positive correlation between high p53 expression and high GPX-1 expression in GCTB. Given that GPX-1 is shown to be a target of p53, these results suggest that p53 mutations play a role in tumor recurrence and malignant transformation of GCTB through interactions with GPX-1.

Indexed as

Cell Transformation, NeoplasticGenes, p53MutationAdolescentAdultAgedBone NeoplasmsCyclin D1FemaleGiant Cell Tumor of BoneGlutathione PeroxidaseGlutathione Peroxidase GPX1HumansImmunohistochemistryLoss of HeterozygosityMaleCCND1 protein, humanCyclin D1Glutathione PeroxidaseGlutathione Peroxidase GPX1GPX1 protein, human

Identifiers

PMID23748877
OpenAlexW2065150226

What OpenQuestion holds

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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.