Evidence map›Paper›PMID 26515726›Full record

ArticleOncotarget2015

Cancer metastasis and EGFR signaling is suppressed by amiodarone-induced versican V2.

Hung-Chieh Lee, Mai-Yan Su, Hao-Chan Lo, Chin-Chieh Wu, Jia-Rung Hu, Dao-Ming Lo, Tsu-Yi Chao, Huai-Jen Tsai, Ming-Shen Dai

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Repurposing Amiodarone for Bladder Cancer Treatment.Cancer research communications · 2025
    Article
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  3. Review
  4. Targeting Ion Channels for Cancer Treatment: Current Progress and Future Challenges.Reviews of physiology, biochemistry and pharmacology · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Three-dimensional culture system identifies a new mode of cetuximab resistance and disease-relevant genes in colorectal cancer.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  13. Article
  14. Review
  15. Article
  16. 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

9 authors at 5 institutions in 1 country.

Hung-Chieh LeeInstitute of Biomedical Sciences, Mackay Medical College, New Taipei City, Taiwan.
Mai-Yan SuInstitute of Molecular and Cellular Biology, College of Life Science, National Taiwan University, Taipei, Taiwan.
Hao-Chan LoInstitute of Molecular and Cellular Biology, College of Life Science, National Taiwan University, Taipei, Taiwan.
Chin-Chieh WuHematology/Oncology, Tri-Service General Hospital, National Defense Medical Centre, Taipei, Taiwan.
Jia-Rung HuInstitute of Biomedical Sciences, Mackay Medical College, New Taipei City, Taiwan.
Dao-Ming LoInstitute of Molecular and Cellular Biology, College of Life Science, National Taiwan University, Taipei, Taiwan.
Tsu-Yi ChaoHematology/Oncology, Shuang-Ho Hospital, Taipei Medical University, Taipei, Taiwan.
Huai-Jen TsaiInstitute of Biomedical Sciences, Mackay Medical College, New Taipei City, Taiwan.
Ming-Shen DaiHematology/Oncology, Tri-Service General Hospital, National Defense Medical Centre, Taipei, Taiwan.
Mackay Medical College · TWNational Taiwan University · TWNational Defense Medical Center · TWTaipei Medical University-Shuang Ho Hospital · TWTri-Service General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular matrix components play an active role in cancer progression and prognosis. Versican, a large extracellular matrix proteoglycan, can promote cancer metastasis through facilitating cell proliferation, adhesion, migration and angiogenesis. We had previously demonstrated that amiodarone caused ectopic overexpression of similar to versican b (s-vcanb), inhibited EGFR/GSK3β/Snail signaling, and enhanced Cdh5 at the heart field of zebrafish, indicating interference with epithelial-mesenchymal transition (EMT). Since S-vcanb is homologous to mammalian versican V2 isoform, we examined the effects of amiodarone on mammalian tumor proliferation, migration, invasion and metastasis in vitro and in vivo and on EMT signaling pathways. Monolayer wound assays and extracellular matrix transwell invasion assays showed reduced migration and invasion by 15 μM amiodarone treated B16OVA, JC, 4T-1, MDA-MB-231 and MCF-7 tumor cell lines. All cancer cell lines showed reduced metastatic capabilities in vivo after treatment with amiodarone in experimental animals. Western blots revealed that EMT-related transcription factors Snail and Twist were reduced and E-cadherin was enhanced in amiodarone treated cells through an EGFR/ERK/GSK3β-dependent pathway. Immunohistochemistry showed amiodarone lead to increased expression of versican V2 isoform concomitant with reduced versican V1. Our study illustrated the role of versican v2 in EMT modulation and cancer suppression by amiodarone treatment.

Indexed as

AmiodaroneAnimalsAntineoplastic AgentsBlotting, WesternCell Line, TumorCell MovementEpithelial-Mesenchymal TransitionErbB ReceptorsFemaleHumansImmunohistochemistryMiceMice, Inbred BALB CMutagenesis, Site-DirectedNeoplasm InvasivenessNeoplasmsAmiodaroneAntineoplastic AgentsErbB ReceptorsVersicansamiodaroneEGFR signalingmetastasisversican

Identifiers

PMID26515726
PMCPMC4767485
OpenAlexW2218299698

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.