Evidence map›Paper›PMID 10773878›Full record

ArticleOncogene2000

Analysis of p73 in human borderline and invasive ovarian tumor.

S W Ng, G K Yiu, Y Liu, L W Huang, M Palnati, S H Jun, R S Berkowitz, S C Mok

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. p73 in Cancer.Genes & cancer · 2011
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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 2 institutions in 1 country.

S W NgLaboratory of Gynecologic Oncology, Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women's Hospital, 221 Longwood Avenue, Boston, Massachusetts, MA 02115, USA.
G K Yiu
Y Liu
L W Huang
M Palnati
S H Jun
R S Berkowitz
S C Mok
Brigham and Women's Hospital · USHarvard University Press · US

Funding

TOPOISOMERASE II EXPRESSION IN DRUG RESISTANCER29CA070216 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI NG, SHU-WING · 1997 to 2001
$237k
PAPILLARY SEROUS CARCINOMA OF THE PERITONEUMR01CA069291 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI MOK, SAMUEL C · 1997 to 2000
$196k
HORMONE REGULATED GENE IN OVARIAN CARCINOGENESISR01CA069453 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI MOK, SAMUEL C · 1997 to 1999
–
NCI NIH HHS CA70216NCI NIH HHS R01CA69291NCI NIH HHS R01CA69453
6 · The paper itself

Abstract

p73 is a novel gene that has high sequence homology and similar gene structure to the tumor suppressor gene p53. We analysed p73 in seven ovarian carcinoma cell lines and a total of 63 human borderline and invasive ovarian tumor samples. Loss of heterozygosity at this locus was observed in 50% of invasive tumors but in none of the borderline tumors. Biallelic expression of the gene was observed in the heterozygous tumor tissues. Direct sequencing and single-strand conformation polymorphism analyses of the p73 cDNA sequence homologous to the highly mutatable region of p53 did not reveal any mutations. When compared to the primary cultures of normal human ovarian surface epithelial cells and immortalized cell lines, four of the seven ovarian carcinoma cell lines, 71% of the invasive tumors, and 92% of the borderline tumor tissues express elevated levels of p73 transcript. Except for the OVCA3 cell line, Western blot analysis of the nuclear extracts prepared from the cell lines showed concordant levels of p73 protein. Our analysis also demonstrated the expression of a spliced variant of p73 transcript with the omission of exon 2 solely in the cancer cell lines and invasive tumor tissues. This exon 2-spliced transcript would give rise to a truncated p73 protein without the N-terminal transactivation domain. In reminiscence of the dominant negative phenotype of the N-terminal truncated variants of another p53-related gene, p63, the expression of the truncated p73 variant form in ovarian tumors may play an important role in the pathogenesis of ovarian cancer.

Indexed as

Genes, Tumor SuppressorAmino Acid SequenceBase SequenceDNA-Binding ProteinsExonsFemaleHumansLoss of HeterozygosityMolecular Sequence DataNeoplasm InvasivenessNuclear ProteinsOvarian NeoplasmsSequence DeletionSequence Homology, Amino AcidTumor Cells, CulturedTumor Protein p73DNA-Binding ProteinsNuclear ProteinsTP73 protein, humanTumor Protein p73Tumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID10773878
OpenAlexW1976571848

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.