Evidence map›Paper›PMID 37711895›Full record

ReviewFrontiers in endocrinology2023

AIB1/SRC-3/NCOA3 function in estrogen receptor alpha positive breast cancer.

Amber J Kiliti, Ghada M Sharif, Mary Beth Martin, Anton Wellstein, Anna T Riegel

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Histone acetylation modulators in breast cancer.Breast cancer research : BCR · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. 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

5 authors.

Amber J KilitiDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, United States.
Ghada M SharifDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, United States.
Mary Beth MartinDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, United States.
Anton WellsteinDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, United States.
Anna T RiegelDepartment of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, United States.

Funding

TRAINING GRANT IN TUMOR BIOLOGYT32CA009686 · NCI · GEORGETOWN UNIVERSITY · PI ANNA Tate RIEGEL, DAVID J ROBBINS · 1996 to 2026
$10.8M
(PQ6) Molecular Mechanisms Driving Benign to Malignant Transitions in Breast CancerR01CA205632 · NCI · GEORGETOWN UNIVERSITY · PI RIEGEL, ANNA TATE · 2016 to 2020
$2.3M
Development of clinically relevant models of DCISR21CA226542 · NCI · GEORGETOWN UNIVERSITY · PI RIEGEL, ANNA TATE · 2019 to 2020
$369k
Decoding the Tissue of Origin of Cellular Damage from Cell-free DNA in Liquid BiopsiesF30CA250307 · NCI · GEORGETOWN UNIVERSITY · PI BAREFOOT, MEGAN EVELYN · 2021 to 2025
$176k
NCI NIH HHS F30 CA250307NCI NIH HHS R01 CA205632NCI NIH HHS R21 CA226542NCI NIH HHS T32 CA009686
6 · The paper itself

Abstract

The estrogen receptor alpha (ERα) is a steroid receptor that is pivotal in the initiation and progression of most breast cancers. ERα regulates gene transcription through recruitment of essential coregulators, including the steroid receptor coactivator AIB1 (Amplified in Breast Cancer 1). AIB1 itself is an oncogene that is overexpressed in a subset of breast cancers and is known to play a role in tumor progression and resistance to endocrine therapy through multiple mechanisms. Here we review the normal and pathological functions of AIB1 in regard to its ERα-dependent and ERα-independent actions, as well as its genomic conservation and protein evolution. We also outline the efforts to target AIB1 in the treatment of breast cancer.

Indexed as

Estrogen Receptor alphaNeoplasmsCognitionGenomicsHumansNuclear Receptor Coactivator 3OncogenesEstrogen Receptor alphaNCOA3 protein, humanNuclear Receptor Coactivator 3AIB1breast cancerendocrine therapyestrogen receptorNcoa3SRC3transcriptional regulation

Identifiers

PMID37711895
PMCPMC10498919

What OpenQuestion holds

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LicenceCC BY
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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.