Evidence map›Paper›PMID 22759378›Full record

ArticleEndocrinology2012

Uterine deletion of Trp53 compromises antioxidant responses in the mouse decidua.

Kristin E Burnum, Yasushi Hirota, Erin S Baker, Mikihiro Yoshie, Yehia M Ibrahim, Matthew E Monroe, Gordon A Anderson, Richard D Smith, Takiko Daikoku, Sudhansu K Dey

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-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

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Role of Inflammaging on the Reproductive Function and Pregnancy.Clinical reviews in allergy & immunology · 2023
    Review
  4. Article
  5. Article
  6. Endometrial Decidualization: The Primary Driver of Pregnancy Health.International journal of molecular sciences · 2020
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. A role for cellular senescence in birth timing.Cell cycle (Georgetown, Tex.) · 2017
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Evidence of perturbations of the cytokine network in preterm labor.American journal of obstetrics and gynecology · 2015
    Article
  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

10 authors at 3 institutions in 1 country.

Kristin E BurnumBiological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99352-9104, USA.
Yasushi Hirota
Erin S Baker
Mikihiro Yoshie
Yehia M Ibrahim
Matthew E Monroe
Gordon A Anderson
Richard D Smith
Takiko Daikoku
Sudhansu K Dey
Pacific Northwest National Laboratory · USUniversity of Cincinnati · USCincinnati Children's Hospital Medical Center · US

Funding

WORKSHOP AND TRAINING ACTIVITIESP41RR018522 · NCRR · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI SMITH, RICHARD D · 2003 to 2011
$25.1M
Equipment Supplement Request for a Research Resource for Ultra-sensitive High Throughput ProteomicsP41GM103493 · NIGMS · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI SMITH, RICHARD D · 2012 to 2022
$22.6M
Molecular signaling in uterine receptivity to implantationR01HD068524 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI Xiaofei Sun · 2011 to 2026
$5.3M
ASPECTS OF BLASTOCYST IMPLANTATIONR37HD012304 · NICHD · VANDERBILT UNIVERSITY · PI DEY, SUDHANSU K · 1999 to 2010
$2.9M
ROLE OF HISTAMINE IN EARLY PREGNANCYR01HD012304 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI DEY, SUDHANSU K · 1985 to 1998
–
NCRR NIH HHS 5P41RR018522-10NCRR NIH HHS P41 RR018522NICHD NIH HHS HD068524NICHD NIH HHS HD12304NICHD NIH HHS R01 HD068524NICHD NIH HHS R37 HD012304NIGMS NIH HHS 8 P41 GM103493-10NIGMS NIH HHS P41 GM103493
6 · The paper itself

Abstract

Preterm birth is a global health issue impacting millions of mothers and babies. However, the etiology of preterm birth is not clearly understood. Our recent finding that premature decidual senescence with terminal differentiation is a cause of preterm birth in mice with uterine Trp53 deletion, encoding p53 protein, led us to explore other potential factors that are related to preterm birth. Using proteomics approaches, here, we show that 183 candidate proteins show significant changes in deciduae with Trp53 deletion as compared with normal deciduae. Functional categorization of these proteins unveiled new pathways that are influenced by p53. In particular, down-regulation of a cluster of antioxidant enzymes in p53-deficient deciduae suggests that increased oxidative stress could be one cause of preterm birth in mice harboring uterine deletion of Trp53.

Indexed as

AnimalsAntioxidantsDeciduaFemaleMiceOxidative StressPremature BirthTumor Suppressor Protein p53UterusAntioxidantsTumor Suppressor Protein p53

Identifiers

PMID22759378
PMCPMC3423619
OpenAlexW2148091556

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.