Evidence map›Paper›PMID 29137354›Full record

ArticleOncotarget2017

ERpS294 is a biomarker of ligand or mutational ERα activation and a breast cancer target for CDK2 inhibition.

Gary K Scott, David Chu, Ravneet Kaur, Julia Malato, Daniel E Rothschild, Katya Frazier, Serenella Eppenberger-Castori, Byron Hann, Ben Ho Park, Christopher C Benz

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. 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
1.8field-weighted citation impact, top 14% 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, 16 citations in OpenAlex.

  1. Article
  2. ESR1 Y537S and D538G Mutations Drive Resistance to CDK4/6 Inhibitors in Estrogen Receptor-Positive Breast Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  3. Article
  4. Review
  5. Estrogen Receptor Alpha and ESR1 Mutations in Breast Cancer.Advances in experimental medicine and biology · 2022
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Circular RNAs in cancer: an emerging key player.Journal of hematology & oncology · 2017
    Review
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 6 institutions in 2 countries.

Gary K Scott *Buck Institute for Research on Aging, Novato, CA, USA.
David Chu *The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Ravneet KaurBuck Institute for Research on Aging, Novato, CA, USA.
Julia MalatoHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Daniel E RothschildBuck Institute for Research on Aging, Novato, CA, USA.
Katya FrazierBuck Institute for Research on Aging, Novato, CA, USA.
Serenella Eppenberger-CastoriInstitute for Pathology, Basel University Hospital, Basel, Switzerland.
Byron HannHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Ben Ho ParkThe Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Christopher C BenzBuck Institute for Research on Aging, Novato, CA, USA.
Buck Institute for Research on Aging · USUniversity of California, San Francisco · USJohns Hopkins Medicine · USJohns Hopkins University · USUCSF Helen Diller Family Comprehensive Cancer Center · USUniversity Hospital of Basel · CH

Funding

The Cancer Genome Atlas Data Analysis CenterU24CA143845 · NCI · BROAD INSTITUTE, INC. · PI CHIN, LYNDA, GETZ, GAD A · 2009 to 2016
$16.0M
UCSC-Buck Inst. Genome Data Analysis Center for TCGA Research Network (GDAC)U24CA143858 · NCI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI BENZ, CHRISTOPHER, HAUSSLER, DAVID H · 2009 to 2016
$8.9M
Mass spectrometry to decode PTM patterns and enhance the Biomarker utility of ERR01CA071468 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI BENZ, CHRISTOPHER · 1996 to 2014
$4.1M
NCI NIH HHS R01 CA071468NCI NIH HHS U24 CA143845NCI NIH HHS U24 CA143858
6 · The paper itself

Abstract

ERα phosphorylation at hinge site S294 (pS294) was recently shown to be essential for ER-dependent gene transcription and mediated by an unknown cyclin-dependent kinase (CDK). This study was undertaken to identify the exact CDK pathway mediating pS294 formation, and to determine if this phosphorylation event occurs with, and can be targeted to treat, the ligand-independent growth of breast cancers expressing endocrine-refractory

Indexed as

cyclin-dependent kinase-2 inhibitorsERα phosphorylationESR1 mutations

Identifiers

PMID29137354
PMCPMC5663526
OpenAlexW2537082914

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.