Evidence map›Paper›PMID 27482544›Full record

ArticleJCI insight2016

Mutant p53 regulates ovarian cancer transformed phenotypes through autocrine matrix deposition.

Marcin P Iwanicki, Hsing-Yu Chen, Claudia Iavarone, Ioannis K Zervantonakis, Taru Muranen, Marián Novak, Tan A Ince, Ronny Drapkin, Joan S Brugge

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
10.6field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Gain-of-function p53Scientific reports · 2023
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Molecular crosstalk between cancer and neurodegenerative diseases.Cellular and molecular life sciences : CMLS · 2020
    Review
  17. Article
  18. Gain-of-Function Mutant p53: All the Roads Lead to Tumorigenesis.International journal of molecular sciences · 2019
    Review
  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

9 authors at 1 institution in 1 country.

Marcin P IwanickiDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Hsing-Yu ChenDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Claudia IavaroneDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Ioannis K ZervantonakisDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Taru MuranenDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Marián NovakDana-Farber Cancer Institute, Department of Medical Oncology, Center for Molecular Oncologic Pathology, Boston, Massachusetts, USA.
Tan A InceStem Cell Institute, University of Miami Miller School of Medicine, Miami, Florida, USA.
Ronny DrapkinDana-Farber Cancer Institute, Department of Medical Oncology, Center for Molecular Oncologic Pathology, Boston, Massachusetts, USA.
Joan S BruggeDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Harvard University · US

Funding

Vaccinating against IGFBP-2 to prevent ovarian cancer relapseP50CA083636 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DRESCHER, CHARLES, URBAN, NICOLE DENISE · 1999 to 2015
$35.1M
Elucidation of the impact of commonly co-altered genes on chemosensitivity using a novel model of high-grade serous ovarian cancerF32CA196008 · NCI · HARVARD MEDICAL SCHOOL · PI CHEN, HSING-YU · 2015 to 2017
$130k
NCI NIH HHS F32 CA196008NCI NIH HHS P50 CA083636
6 · The paper itself

Abstract

High-grade serous ovarian carcinoma (HGS-OvCa) harbors p53 mutations and can originate from the epithelial cell compartment of the fallopian tube fimbriae. From this site, neoplastic cells detach, survive in the peritoneal cavity, and form cellular clusters that intercalate into the mesothelium to form ovarian and peritoneal masses. To examine the contribution of mutant p53 to phenotypic alterations associated with HGS-OvCA, we developed live-cell microscopy assays that recapitulate these early events in cultured fallopian tube nonciliated epithelial (FNE) cells. Expression of stabilizing mutant variants of p53, but not depletion of endogenous wild-type p53, in FNE cells promoted survival and cell-cell aggregation under conditions of cell detachment, leading to the formation of cell clusters with mesothelium-intercalation capacity. Mutant p53

Identifiers

PMID27482544
PMCPMC4963159
OpenAlexW2463378434

What OpenQuestion holds

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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.