Evidence map›Paper›PMID 27556500›Full record

ArticleOncotarget2016

The ELK3-GATA3 axis orchestrates invasion and metastasis of breast cancer cells in vitro and in vivo.

Sun-Young Kong, Kwang-Soo Kim, Jiewan Kim, Min Kyeong Kim, Ki Hong Lee, Je-Yong Lee, Nuri Oh, Ji-In Park, Ji-Hoon Park, Sun-Hee Heo and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.0field-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

25 citing papers in PubMed, 45 citations in OpenAlex.

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  12. [Expression characteristics and functional analysis of ELK3 in gastric cancer].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
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  17. Frontiers in oncology · 2021
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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

14 authors at 3 institutions in 1 country.

Sun-Young KongDepartment of System Cancer Science, Graduate School of Cancer Science and Policy, National Cancer Center, Seoul, Korea.
Kwang-Soo KimDepartment of Biomedical Science, College of Life Science, CHA University, Seoul, Korea.
Jiewan KimDepartment of Biomedical Science, College of Life Science, CHA University, Seoul, Korea.
Min Kyeong KimDepartment of System Cancer Science, Graduate School of Cancer Science and Policy, National Cancer Center, Seoul, Korea.
Ki Hong LeeDepartment of System Cancer Science, Graduate School of Cancer Science and Policy, National Cancer Center, Seoul, Korea.
Je-Yong LeeDepartment of Biomedical Science, College of Life Science, CHA University, Seoul, Korea.
Nuri OhDepartment of Biomedical Science, College of Life Science, CHA University, Seoul, Korea.
Ji-In ParkDepartment of Biomedical Science, College of Life Science, CHA University, Seoul, Korea.
Ji-Hoon ParkDepartment of Biomedical Science, College of Life Science, CHA University, Seoul, Korea.
Sun-Hee HeoBiomedical Research Center, Asan Institute for Science and Department of Pathology, Asan Medical Center, University of Ulsan, College of Medicine, Ulsan, Korea.
Sung Han ShimDepartment of Biomedical Science, College of Life Science, CHA University, Seoul, Korea.
Dong Ryul LeeDepartment of Biomedical Science, College of Life Science, CHA University, Seoul, Korea.
Keun Pil KimDepartment of Life Science, Chung-Ang University, Seoul, Korea.
Kyung-Soon ParkDepartment of Biomedical Science, College of Life Science, CHA University, Seoul, Korea.
CHA University · KRNational Cancer Center · KRChung-Ang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer is a highly aggressive tumor subtype that lacks effective therapeutic targets. Here, we show that ELK3 is overexpressed in a subset of breast cancers, in particular basal-like and normal-like/claudin-low cell lines. Suppression of ELK3 in MDA-MB-231 cells led to transdifferentiation from an invasive mesenchymal phenotype to a non-invasive epithelial phenotype both in vitro and in vivo. Suppression of ELK3 resulted in extensive changes in genome expression profiles. Among these, GATA3, a master suppressor of metastasis, was epigenetically activated. Also, suppression of GATA3 led to the restoration of migration and invasion. These results suggest that the ELK3-GATA3 axis is a major pathway that promotes metastasis of MDA-MB-231 cells.

Indexed as

AnimalsCell Line, TumorCell MovementCell TransdifferentiationFemaleGATA3 Transcription FactorHeterograftsHumansMiceMice, Inbred NODMice, SCIDNeoplasm InvasivenessProto-Oncogene ProteinsProto-Oncogene Proteins c-etsTranscription FactorsTriple Negative Breast NeoplasmsElk3 protein, humanGATA3 protein, humanGATA3 Transcription FactorProto-Oncogene ProteinsProto-Oncogene Proteins c-etsTranscription FactorsELK3GATA3invasionmetastasismigration

Identifiers

PMID27556500
PMCPMC5323143
OpenAlexW2508803302

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.