Evidence map›Paper›PMID 23948299›Full record

ArticleCancer cell2013

Amplification of distant estrogen response elements deregulates target genes associated with tamoxifen resistance in breast cancer.

Pei-Yin Hsu, Hang-Kai Hsu, Xun Lan, Liran Juan, Pearlly S Yan, Jadwiga Labanowska, Nyla Heerema, Tzu-Hung Hsiao, Yu-Chiao Chiu, Yidong Chen and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Loss of ZIP facilitates JAK2-STAT3 activation in tamoxifen-resistant breast cancer.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. CTCF, Cohesin, and Chromatin in Human Cancer.Genomics & informatics · 2017
    Review
  19. Review
  20. Article
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

19 authors at 7 institutions in 2 countries.

Pei-Yin HsuDepartment of Molecular Medicine/Institute of Biotechnology, Cancer Therapy and Research Center, The University of Texas Health Science Center at San Antonio, San Antonio, TX 78245, USA.
Hang-Kai Hsu
Xun Lan
Liran Juan
Pearlly S Yan
Jadwiga Labanowska
Nyla Heerema
Tzu-Hung Hsiao
Yu-Chiao Chiu
Yidong Chen
Yunlong Liu
Lang Li
Rong Li
Ian M Thompson
Kenneth P Nephew
Zelton D Sharp
Nameer B Kirma
Victor X Jin
Tim H-M Huang
The University of Texas Health Science Center at San Antonio · USThe Ohio State University · USIndiana University School of MedicineCancer Research Institute · USIndiana University Bloomington · USIndiana University – Purdue University Indianapolis · USNational Taiwan University · TW

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
Predicting Drug Resistance in Cancer Genomes by DMA Methylation ProfilingU54CA113001 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HUANG, TIM H.-M. · 2004 to 2014
$16.1M
DNA Hypermethylation in Breast CancerR01CA069065 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HUANG, TIM H.-M. · 2002 to 2011
$2.4M
Epigenomics of Bisphenol A Exposure and Disease RiskR01ES017594 · NIEHS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HUANG, TIM H.-M. · 2009 to 2013
$1.8M
Environmental Epigenetics and Stem/Progenitor Cell InjuryU01ES015986 · NIEHS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HUANG, TIM H.-M. · 2007 to 2010
$1.5M
Regulation of hormone production by matrix proteinsR01CA161349 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LI, RONG · 2012 to 2016
$1.5M
NCI NIH HHS P30 CA054174NCI NIH HHS R01 CA069065NCI NIH HHS R01 CA161349NCI NIH HHS U54 CA113001NIEHS NIH HHS R01 ES017594NIEHS NIH HHS U01 ES015986
6 · The paper itself

Abstract

A causal role of gene amplification in tumorigenesis is well known, whereas amplification of DNA regulatory elements as an oncogenic driver remains unclear. In this study, we integrated next-generation sequencing approaches to map distant estrogen response elements (DEREs) that remotely control the transcription of target genes through chromatin proximity. Two densely mapped DERE regions located on chromosomes 17q23 and 20q13 were frequently amplified in estrogen receptor-α-positive luminal breast cancer. These aberrantly amplified DEREs deregulated target gene expression potentially linked to cancer development and tamoxifen resistance. Progressive accumulation of DERE copies was observed in normal breast progenitor cells chronically exposed to estrogenic chemicals. These findings may extend to other DNA regulatory elements, the amplification of which can profoundly alter target transcriptome during tumorigenesis.

Indexed as

Gene Expression Regulation, NeoplasticResponse ElementsAntineoplastic Agents, HormonalBreast NeoplasmsCell Line, TumorDrug Resistance, NeoplasmEstrogen Receptor alphaEstrogensFemaleGene AmplificationGenomicsHumansTamoxifenAntineoplastic Agents, HormonalEstrogen Receptor alphaEstrogensTamoxifen

Identifiers

PMID23948299
PMCPMC3890247
OpenAlexW2056279621

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.