Evidence map›Paper›PMID 23933151›Full record

ReviewMolecular and cellular endocrinology2014

PELP1: a review of PELP1 interactions, signaling, and biology.

Brian J Girard, Andrea R Daniel, Carol A Lange, Julie H Ostrander

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular and cellular endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 59 citations in OpenAlex.

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  16. Overexpression of PELP1 in Lung Adenocarcinoma Promoted EPathology oncology research : POR · 2021
    Article
  17. Article
  18. Fragile GeneFrontiers in oncology · 2021
    Article
  19. 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

4 authors at 1 institution in 1 country.

Brian J GirardMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, United States.
Andrea R DanielMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, United States.
Carol A LangeMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, United States.
Julie H OstranderMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, United States. Electronic address: hans1354@umn.edu.
University of Minnesota Medical Center · US

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
Role of Phospho-Progesterone Receptors (PR) in Hormone Refractory Breast CancerR01CA159712 · NCI · UNIVERSITY OF MINNESOTA · PI LANGE, CAROL A · 2012 to 2016
$1.9M
Does Cytoplasmic PELP1 Predict Resistance To Tamoxifen Chemoprevention?K07CA131501 · NCI · UNIVERSITY OF MINNESOTA · PI OSTRANDER, JULIE H · 2010 to 2014
$580k
NCATS NIH HHS UL1 TR000114NCATS NIH HHS UL1TR000114NCI NIH HHS K07 CA131501NCI NIH HHS K07CA131501-02NCI NIH HHS R01 CA159712
6 · The paper itself

Abstract

Proline, glutamic acid, and leucine rich protein 1 (PELP1) is a large multi-domain protein that has been shown to modulate an increasing number of pathways and biological processes. The first reports describing the cloning and characterization of PELP1 showed that it was an estrogen receptor coactivator. PELP1 has now been shown to be a coregulator for a growing number of transcription factors. Furthermore, recent reports have shown that PELP1 is a member of chromatin remodeling complexes. In addition to PELP1 nuclear functions, it has been shown to have cytoplasmic signaling functions as well. In the cytoplasm PELP1 acts as a scaffold molecule and mediates rapid signaling from growth factor and hormone receptors. PELP1 signaling ultimately plays a role in cancer biology by increasing proliferation and metastasis, among other cellular processes. Here we will review (1) the cloning and characterization of PELP1 expression, (2) interacting proteins, (3) PELP1 signaling, and (4) PELP1-mediated biology.

Indexed as

Signal TransductionAnimalsCell NucleusHumansModels, BiologicalMolecular Targeted TherapyProtein BindingTranscription FactorsTranscription FactorsAIB1amplified in breast cancer 1androgen receptorARBCAS3breast carcinoma amplified sequence 3CBPChIPchromatin immunoprecipitationCoactivatorCREB binding proteinc-Src homology domain 2c-Src homology domain 3E2ERERRαestradiolestrogen receptorestrogen-related receptor alphaEstrogen signalingExtra-nuclear signalingFHL2four and a half LIM domains 2glucocorticoid receptorGRHDAChistone deacetylaseHormone resistanceIHCILK1immunohistochemistryintegrin-linked kinase 1KDM1LIM domainLin-1, Isl-1, and Mec-3 domainlysine-specific histone demethylase 1MNARModulator of Nongenomic Activity of ERPELP1proline, glutamic acid and leucine rich protein 1retinoid X receptorRXRSH2SH3signal transducer and activator or transcription 3STAT3TIF2transcriptional mediators/intermediary factor 2

Identifiers

PMID23933151
PMCPMC3844065
OpenAlexW2072613049

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.