Evidence map›Paper›PMID 24166501›Full record

ArticleOncogene2014

Aurora-A is a determinant of tamoxifen sensitivity through phosphorylation of ERα in breast cancer.

X Q Zheng, J P Guo, H Yang, M Kanai, L L He, Y Y Li, J M Koomen, S Minton, M Gao, X B Ren and 2 more

RetractedAbstract readRetracted Publication
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Seize the engine: Emerging cell cycle targets in breast cancer.Clinical and translational medicine · 2024
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. OTUD6A Is an Aurora Kinase A-Specific Deubiquitinase.International journal of molecular sciences · 2021
    Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

X Q Zheng1] Department of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA [2] Departments of Thyroid and Neck Tumour, Tianjin Medical University Cancer Institute and Hospital, Oncology Key Laboratory of cancer prevention and therapy, National Clinical Research Center of Cancer, Tianjin, PR China [3] Department of Immunology, Tianjin Medical University Cancer Institute and Hospital, Oncology Key Laboratory of cancer prevention and therapy, National Clinical Research Center of Cancer, Tianjin, PR China.
J P GuoDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
H YangDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
M KanaiDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
L L HeDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
Y Y LiDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
J M KoomenDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
S MintonDepartments of Women's Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
M GaoDepartments of Thyroid and Neck Tumour, Tianjin Medical University Cancer Institute and Hospital, Oncology Key Laboratory of cancer prevention and therapy, National Clinical Research Center of Cancer, Tianjin, PR China.
X B RenDepartment of Immunology, Tianjin Medical University Cancer Institute and Hospital, Oncology Key Laboratory of cancer prevention and therapy, National Clinical Research Center of Cancer, Tianjin, PR China.
D CoppolaDepartments of Women's Pathology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
J Q ChengDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
Moffitt Cancer Center · USMolecular Oncology (United States) · USTianjin Medical University Cancer Institute and Hospital · CN

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
IKBKE/IKKE (epsilon) Kinase in Non-small Cell Lung CancerR01CA160455 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI CHENG, JIN Q · 2012 to 2016
$1.7M
MicroRNAs in Human Ovarian CancerR01CA137041 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI CHENG, JIN Q · 2009 to 2013
$1.7M
NCI NIH HHS CA160455NCI NIH HHS P30 CA076292NCI NIH HHS R01 CA137041NCI NIH HHS R01 CA160455
6 · The paper itself

Abstract

Despite the clinical success of tamoxifen, its resistance remains a major challenge in breast cancer. Here we show that Aurora-A determines tamoxifen sensitivity by regulation of oestrogen receptor (ER)α. Ectopic expression of Aurora-A decreases and depletion of Aurora-A enhances tamoxifen sensitivity in ERα-positive breast cancer. Elevated Aurora-A was significantly associated with the recurrence of ERα-positive tumours. Notably, Aurora-A inhibitor MLN8237, which is currently in clinical trial, synergizes with tamoxifen and overcomes tamoxifen resistance. Furthermore, Aurora-A interacts with and phosphorylates ERα on serine-167 and -305, leading to increase in ERα DNA-binding and transcriptional activity. Elevated levels of Aurora-A are significantly associated with disease-free survival in ERα-positive but not ERα-negative breast cancers. These data suggest that Aurora-A has a pivotal role in tamoxifen resistance and ERα is a bona fide substrate of Aurora-A. Thus, Aurora-A represents a prognostic marker in ERα-positive tumour and a critical therapeutic target in tamoxifen-resistant breast cancer, and Aurora-A inhibitor could be used as either an independent or concurrent agent in tamoxifen-resistant tumour.

Indexed as

Protein Processing, Post-TranslationalAnimalsAntineoplastic Agents, HormonalAurora Kinase AAzepinesBreast NeoplasmsCell Line, TumorCyclin D1Disease-Free SurvivalDrug Resistance, NeoplasmDrug SynergismEstrogen Receptor alphaFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansAntineoplastic Agents, HormonalAURKA protein, humanAurora Kinase AAzepinesCCND1 protein, humanCyclin D1ESR1 protein, humanEstrogen Receptor alphaMLN 8237PyrimidinesTamoxifen

Identifiers

PMID24166501
PMCPMC4002670
OpenAlexW2037463541

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.