Evidence map›Paper›PMID 28925396›Full record

ArticleOncogene2018

MIG-6 negatively regulates STAT3 phosphorylation in uterine epithelial cells.

J-Y Yoo, W S Yang, J H Lee, B G Kim, R R Broaddus, J M Lim, T H Kim, J-W Jeong

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Expression of PIK3IP1 in the murine uterus during early pregnancy.Biochemical and biophysical research communications · 2018
    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 3 institutions in 2 countries.

J-Y YooDepartment of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, College of Human Medicine, Grand Rapids, MI, USA.
W S YangDepartment of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, College of Human Medicine, Grand Rapids, MI, USA.
J H LeeDepartment of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, College of Human Medicine, Grand Rapids, MI, USA.
B G KimDepartment of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, College of Human Medicine, Grand Rapids, MI, USA.
R R BroaddusDepartment of Pathology, University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
J M LimDepartment of Agricultural Biotechnology, Seoul National University, Seoul, South Korea.
T H KimDepartment of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, College of Human Medicine, Grand Rapids, MI, USA.
J-W JeongDepartment of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, College of Human Medicine, Grand Rapids, MI, USA.
Michigan State University · USSeoul National University · KRThe University of Texas MD Anderson Cancer Center · US

Funding

Risk factors for early pregnancy lossR01HD084478 · NICHD · MICHIGAN STATE UNIVERSITY · PI JEONG, JAE-WOOK · 2016 to 2020
$1.6M
NICHD NIH HHS R01 HD084478
6 · The paper itself

Abstract

Endometrial cancer is the most common malignancy of the female genital tract. Progesterone (P4) has been used for several decades in endometrial cancer treatment, especially in women who wish to retain fertility. However, it is unpredictable which patients will respond to P4 treatment and which may have a P4-resistant cancer. Therefore, identifying the mechanism of P4 resistance is essential to improve the therapies for endometrial cancer. Mitogen-inducible gene 6 (Mig-6) is a critical mediator of progesterone receptor (PGR) action in the uterus. In order to study the function of Mig-6 in P4 resistance, we generated a mouse model in which we specifically ablated Mig-6 in uterine epithelial cells using Sprr2f-cre mice (Sprr2f

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCell Line, TumorDrug Resistance, NeoplasmEndometrial NeoplasmsFemaleHumansIntracellular Signaling Peptides and ProteinsMiceMice, KnockoutPhosphorylationProgesteroneReceptors, ProgesteroneSignal TransductionSTAT3 Transcription FactorTumor Suppressor ProteinsAdaptor Proteins, Signal TransducingERRFI1 protein, humanErrfi1 protein, mouseIntracellular Signaling Peptides and ProteinsProgesteroneReceptors, ProgesteroneSTAT3 protein, humanStat3 protein, mouseSTAT3 Transcription FactorTumor Suppressor Proteins

Identifiers

PMID28925396
PMCPMC5764811
OpenAlexW2754456728

What OpenQuestion holds

Textmetadata
LicenceTDM
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.