Evidence map›Paper›PMID 15897900›Full record

ArticleOncogene2005

Pituitary tumour transforming gene (PTTG) induces genetic instability in thyroid cells.

Dae Kim, Helen Pemberton, Anna L Stratford, Kristien Buelaert, John C Watkinson, Victor Lopes, Jayne A Franklyn, Chris J McCabe

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 79 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Thyroid hormone receptors and cancer.Biochimica et biophysica acta · 2013
    Review
  10. Thyroid hormone actions in liver cancer.Cellular and molecular life sciences : CMLS · 2013
    Review
  11. Article
  12. The pituitary tumor transforming gene in thyroid cancer.Journal of endocrinological investigation · 2012
    Review
  13. Article
  14. Targeting zebrafish and murine pituitary corticotroph tumors with a cyclin-dependent kinase (CDK) inhibitor.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  15. Pathogenesis of pituitary tumors.Nature reviews. Endocrinology · 2011
    Review
  16. Fifteen years' experience in thyroid surgery.Annals of the Royal College of Surgeons of England · 2010
    Article
  17. Pituitary senescence: the evolving role of Pttg.Molecular and cellular endocrinology · 2010
    Review
  18. Article
  19. Review
  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

8 authors at 1 institution in 1 country.

Dae KimDivision of Medical Sciences, 2nd Floor IBR, University of Birmingham, Edgbaston, Birmingham B12 5TT, UK. daekim72@yahoo.co.uk
Helen Pemberton
Anna L Stratford
Kristien Buelaert
John C Watkinson
Victor Lopes
Jayne A Franklyn
Chris J McCabe
University of Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer reflects the progressive accumulation of genetic alterations and subsequent genetic instability of cells. Cytogenetic studies have demonstrated the importance of aneuploidy in differentiated thyroid cancer development. The pituitary tumour transforming gene (PTTG), also known as securin, is a mitotic checkpoint protein which inhibits sister chromatid separation during mitosis. PTTG is highly expressed in many cancers and overexpression of PTTG induces aneuploidy in vitro. Using fluorescent intersimple sequence repeat PCR (FISSR-PCR), we investigated the relationship between PTTG expression and the degree of genetic instability in normal and tumorous thyroid samples. The genomic instability index (GI index) was 6.7-72.7% higher in cancers than normal thyroid tissues. Follicular thyroid tumours exhibited greater genetic instability than papillary tumours (27.6% (n=9) versus 14.5% (n=10), P=0.03). We also demonstrated a strong relationship between PTTG expression and the degree of genetic instability in thyroid cancers (R2=0.80, P=0.007). To further investigate PTTG's role in genetic instability, we transfected FTC133 thyroid follicular cells and observed increased genetic instability in cells overexpressing PTTG compared with vector-only-transfected controls (n=3, GI Index VO=29.7+/-5.2 versus PTTG=63.7+/-6.4, P=0.013). Further, we observed a dose response in genetic instability and PTTG expression (GI Index low dose (0.5 microg DNA/ six-well plate) PTTG=15.3%+/-1.7 versus high dose (3 microg DNA) PTTG=50.8%+/-3.3, P=0.006). Overall, we describe the first use of FISSR-PCR in human cancers, and demonstrate that PTTG expression correlates with genetic instability in vivo, and induces genetic instability in vitro. We conclude that PTTG may be an important gene in the mutator phenotype development in thyroid cancer.

Indexed as

Genomic InstabilityCaspase 3Caspase 7CaspasesCell LineHumansNeoplasm ProteinsRNA, MessengerSecurinThyroid GlandThyroid NeoplasmsCASP3 protein, humanCASP7 protein, humanCaspase 3Caspase 7CaspasesNeoplasm Proteinspituitary tumor-transforming protein 1, humanRNA, MessengerSecurin

Identifiers

PMID15897900
OpenAlexW2166086329

What OpenQuestion holds

Textmetadata
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.