Evidence map›Paper›PMID 25048580›Full record

ArticlePloS one2014

Real-time imaging of the epithelial-mesenchymal transition using microRNA-200a sequence-based molecular beacon-conjugated magnetic nanoparticles.

YoonSeok Choi, Hoe Suk Kim, Jisu Woo, Eun Hye Hwang, Kyoung-Won Cho, Soonhag Kim, Woo Kyung Moon

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. EMT in cancer.Nature reviews. Cancer · 2018
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. 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

7 authors at 3 institutions in 1 country.

YoonSeok ChoiDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Jongro-gu, Seoul, Republic of Korea; Department of Radiology, Seoul National University Hospital, Jongro-gu, Seoul, Republic of Korea.
Hoe Suk KimDepartment of Radiology, Seoul National University Hospital, Jongro-gu, Seoul, Republic of Korea; The Institute of Radiation Medicine, Medical Research Center, Seoul National University, Jongro-gu, Seoul, Republic of Korea.
Jisu WooDepartment of Radiology, Seoul National University Hospital, Jongro-gu, Seoul, Republic of Korea.
Eun Hye HwangDepartment of Radiology, Seoul National University Hospital, Jongro-gu, Seoul, Republic of Korea.
Kyoung-Won ChoDepartment of Radiology, Seoul National University Hospital, Jongro-gu, Seoul, Republic of Korea; The Institute of Radiation Medicine, Medical Research Center, Seoul National University, Jongro-gu, Seoul, Republic of Korea.
Soonhag KimDepartment of Biomedical Sciences, College of Biomedical Sciences, CHA University, Gangnam-gu, Seoul, Republic of Korea.
Woo Kyung MoonDepartment of Biomedical Sciences, College of Medicine, Seoul National University, Jongro-gu, Seoul, Republic of Korea; Department of Radiology, Seoul National University Hospital, Jongro-gu, Seoul, Republic of Korea; The Institute of Radiation Medicine, Medical Research Center, Seoul National University, Jongro-gu, Seoul, Republic of Korea.
Seoul National University · KRSeoul National University Hospital · KRCHA University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epithelial-mesenchymal transition (EMT) plays important roles in tumor progression to metastasis. Thus, the development of an imaging probe that can monitor transient periods of the EMT process in live cells is required for a better understanding of metastatic process. Inspired by the fact that the mRNA expression levels of zinc finger E-box-binding homeobox 1 (ZEB1) increase when cells adopt mesenchyme characteristics and that microRNA-200a (miR-200a) can bind to ZEB1 mRNA, we conjugated molecular beacon (MB) mimicking mature miR-200a to magnetic nanoparticles (miR-200a-MB-MNPs) and devised an imaging method to observe transitional changes in the cells during EMT. Transforming growth factor-β1 treated epithelial cells and breast cancer cell lines representing both epithelial and mesenchymal phenotypes were used for the validation of miR-200a-MB-MNPs as an EMT imaging probe. The real-time imaging of live cells acquired with the induction of EMT revealed an increase in fluorescence signals by miR-200a-MB-MNPs, cell morphology alterations, and the loss of cell-cell adhesion. Our results suggest that miR-200a-MB-MNPs can be used as an imaging probe for the real-time monitoring of the EMT process in live cells.

Indexed as

Epithelial-Mesenchymal TransitionMagnetite NanoparticlesMicroRNAsAnimalsBase SequenceCell LineCell Line, TumorDogsHumansMiceOptical ImagingMagnetite NanoparticlesMicroRNAsMIRN200 microRNA, human

Identifiers

PMID25048580
PMCPMC4105468
OpenAlexW2002256744

What OpenQuestion holds

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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.