Evidence map›Paper›PMID 23486015›Full record

ArticleCarcinogenesis2013

PELP1 oncogenic functions involve CARM1 regulation.

Monica Mann, Valerie Cortez, Ratna Vadlamudi

Open access · bronzeAbstract read
In one paragraph

Article in Carcinogenesis, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

45 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
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  9. Dysregulation of arginine methylation in tumorigenesis.Frontiers in molecular biosciences · 2024
    Review
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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

3 authors at 1 institution in 1 country.

Monica MannDepartment of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Valerie Cortez
Ratna Vadlamudi
The University of Texas Health Science Center at San Antonio · US

Funding

PELP1, a Novel Regulator of Estrogen ReceptorR01CA095681 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI VADLAMUDI, RATNA K · 2003 to 2013
$2.5M
Significance of PELP1 in Breast Cancer ProgressionF31CA165814 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CORTEZ, VALERIE ANN · 2011 to 2013
$56k
Epigenetic Regulation of Breast Cancer Progression by the Proto-oncogene PELP1F31CA173909 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI MANN, MONICA · 2013 to 2013
$23k
NCI NIH HHS 1F31CA165814NCI NIH HHS 1F31CA173909NCI NIH HHS CA095681
6 · The paper itself

Abstract

Estrogen receptor alpha (ERα) is implicated in the initiation and progression of breast cancer and its transcription depends on the modulation of epigenetic changes at target gene promoters via coregulators. There is a critical need to understand the molecular mechanism(s) by which deregulation of epigenetic changes occurs during breast cancer progression. The ERα coregulator PELP1 plays an important role in ERα signaling and is a proto-oncogene with aberrant expression in breast cancer. PELP1 interacts with histones and may be a reader of chromatin modifications. We profiled PELP1's epigenetic interactome using a histone peptide array. Our results show that PELP1 recognizes histones modified by arginine and lysine dimethylation. PELP1 functionally interacts with the arginine methyltransferase CARM1 and their interaction is enhanced by ERα. PELP1-CARM1 interactions synergistically enhance ERα transactivation. Chromatin immunoprecipitation assays revealed that PELP1 alters histone H3 arginine methylation status at ERα target gene promoters. Pharmacological inhibition or small interfering RNA knockdown of CARM1 substantially reduced PELP1 oncogenic functions. The critical role of PELP1 status in modulating arginine methylation status was also observed through in vivo studies where PELP1 knockdown mediated decreased tumorigenesis correlated with decreased arginine dimethylation. Further, immunohistochemical analysis of human breast tumor tissues revealed co-overexpression of PELP1 and CARM1 in a subset of ERα-positive breast tumors. Our findings show PELP1 is a reader of histone arginine methyl modifications and deregulation promotes tumor proliferation via epigenetic alterations at ERα target promoters. Targeting these epigenetic alterations through inhibition of PELP1 and the arginine methyltransferases could be a promising cancer therapeutic.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsArginineBreast NeoplasmsChromatin ImmunoprecipitationCo-Repressor ProteinsEnzyme InhibitorsEpigenesis, GeneticEstrogen Receptor alphaFemaleHistonesHumansImmunohistochemistryMCF-7 CellsMethylationMiceArgininecoactivator-associated arginine methyltransferase 1Co-Repressor ProteinsEnzyme InhibitorsESR1 protein, humanEstrogen Receptor alphaHistonesMAS1 protein, humanPELP1 protein, humanProtein-Arginine N-MethyltransferasesProto-Oncogene MasProto-Oncogene ProteinsRNA, Small InterferingTranscription Factors

Identifiers

PMID23486015
PMCPMC3697892
OpenAlexW2141312827

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.