Evidence map›Paper›PMID 34528025›Full record

ArticleExploration of targeted anti-tumor therapy2021

Role of estrogen receptor coregulators in endocrine resistant breast cancer.

Kristin A Altwegg, Ratna K Vadlamudi

Open access · diamondAbstract read
In one paragraph

Article in Exploration of targeted anti-tumor therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Signal Crosstalk and the Role of Estrogen Receptor beta (ERβ) in Prostate Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2022
    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

2 authors at 1 institution in 1 country.

Kristin A AltweggDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0002-3439-0655
Ratna K VadlamudiDepartment of Obstetrics and Gynecology, University of Texas Health San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0003-2849-4076
The University of Texas Health Science Center at San Antonio · US

Funding

Therapeutic agents targeting nuclear receptor signaling in distinct molecular subtypes of breast cancerR01CA223828 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI RAJ, GANESH V, VADLAMUDI, RATNA K · 2018 to 2022
$3.0M
FoXM1 inhibition: a novel therapeutic avenue to treat breast cancersR01CA239227 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI RAO, MANJEET KUMAR, VADLAMUDI, RATNA K · 2020 to 2024
$2.1M
Development of Small Molecule Inhibitor of PELP1 for Treating Advanced Breast CancerF31CA257298 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ALTWEGG, KRISTIN ANN · 2021 to 2022
$51k
NCI NIH HHS F31 CA257298NCI NIH HHS R01 CA223828NCI NIH HHS R01 CA239227
6 · The paper itself

Abstract

Breast cancer (BC) is the most ubiquitous cancer in women. Approximately 70-80% of BC diagnoses are positive for estrogen receptor (ER) alpha (ERα). The steroid hormone estrogen [17β-estradiol (E2)] plays a vital role both in the initiation and progression of BC. The E2-ERα mediated actions involve genomic signaling and non-genomic signaling. The specificity and magnitude of ERα signaling are mediated by interactions between ERα and several coregulator proteins called coactivators or corepressors. Alterations in the levels of coregulators are common during BC progression and they enhance ligand-dependent and ligand-independent ERα signaling which drives BC growth, progression, and endocrine therapy resistance. Many ERα coregulator proteins function as scaffolding proteins and some have intrinsic or associated enzymatic activities, thus the targeting of coregulators for blocking BC progression is a challenging task. Emerging data from

Indexed as

coregulatorsendocrine therapy resistanceestrogenEstrogen receptorhormonal actionsignal transductiontranscriptional activation

Identifiers

PMID34528025
PMCPMC8439438
OpenAlexW3197832970

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.