Evidence map›Paper›PMID 17415682›Full record

ArticleMolecular biology reports2008

A novel gene STYK1/NOK is upregulated in estrogen receptor-alpha negative estrogen receptor-beta positive breast cancer cells following estrogen treatment.

K Sean Kimbro, Kaitlin Duschene, Margeret Willard, Jodi-Ann Moore, Shalonda Freeman

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2008. 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
1.4field-weighted citation impact, top 17% 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, 29 citations in OpenAlex.

  1. Depletion of STYK1 inhibits intrahepatic cholangiocarcinoma development both in vitro and in vivo.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Trial
  2. Article
  3. Article
  4. Joint Screening for Ultra-High Dimensional Multi-Omics Data.Bioengineering (Basel, Switzerland) · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

5 authors at 2 institutions in 1 country.

K Sean KimbroDepartment of Hematology and Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA 30322, USA. sean.kimbro@emoryhealthcare.org
Kaitlin Duschene
Margeret Willard
Jodi-Ann Moore
Shalonda Freeman
Emory University · USClark Atlanta University · US

Funding

THEORY OF PLANNED BEHAVIOR VS ETHNICITY /PHYSICAL ACTIVIG12RR003062 · NCRR · CLARK ATLANTA UNIVERSITY · PI BROWN, CARLTON B · 1985 to 2011
$15.5M
Research Initiative for Scientific Enhancement (RISE)R25GM060414 · NIGMS · CLARK ATLANTA UNIVERSITY · PI MUSEY, PAUL I. · 1999 to 2020
$13.7M
VIRTUAL REALITY TECHNOLOGY IN TREATMENT OF FEARS AND PHOBIASS06GM008247 · NIGMS · CLARK ATLANTA UNIVERSITY · PI KHAN, ISHRAT M · 1989 to 2008
$6.6M
Genomic and Proteomic Study of Cancer Disparities in Et*P20CA091366 · NCI · CLARK ATLANTA UNIVERSITY · PI KIMBRO, KEVIN SEAN · 2002 to 2003
$338k
NCI NIH HHS P20CA091366NCRR NIH HHS G12RR003062NIGMS NIH HHS R25GM060414NIGMS NIH HHS S06GM008247
6 · The paper itself

Abstract

The human STYK1/NOK protein is approximately 30-35% similar to mouse fibroblast growth factor receptor 3 and a kinase homologue in D. melanogaster in the tyrosine protein kinase region. STYK1/NOK was identified as being up regulated in MDA-MB-231, an estrogen receptor-alpha negative breast cancer cell line, following 12 h of estrogen treatment at 1x10(-9) M. On further investigation of STYK1/NOK in estrogen treated cell line MDA-MB-231, STYK1/NOK was up regulated at 6 h post treatment when compared to untreated cells. We also investigated the expression levels of STYK1/NOK in other breast cancer cell lines MCF-7, MDA-MB-231, BT-549, and MDA-MB-435S using QRT-PCR. In addition, the analysis of message accumulation was increased with other synthetic estrogen response modifiers. We propose that the regulation of STYK1/NOK is achieved independent of ERalpha and suggests further investigation to the relevance of this kinase in breast cancer progression.

Indexed as

Breast NeoplasmsCell Line, TumorEstrogen Receptor alphaEstrogen Receptor betaEstrogen Receptor ModulatorsEstrogensGene Expression Regulation, NeoplasticHumansReceptor Protein-Tyrosine KinasesRNA, MessengerTime FactorsUp-RegulationEstrogen Receptor alphaEstrogen Receptor betaEstrogen Receptor ModulatorsEstrogensReceptor Protein-Tyrosine KinasesRNA, MessengerSTYK1 protein, human

Identifiers

PMID17415682
OpenAlexW2049179098

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.