Evidence map›Paper›PMID 26572230›Full record

ArticleJournal of biomedical science2015

Activation of MEK2 is sufficient to induce skin papilloma formation in transgenic zebrafish.

Chih-Ming Chou, Yi-Chung Chen, San Su, Gen-Der Chen, Kai-Yun Huang, Huang-Wei Lien, Chang-Jen Huang, Chia-Hsiung Cheng

Open access · diamondAbstract read
In one paragraph

Article in Journal of biomedical science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 93% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

8 authors at 2 institutions in 1 country.

Chih-Ming ChouDepartment of Biochemistry and Molecular Cell Biology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, 110, Taiwan. cmchou@tmu.edu.tw.
Yi-Chung ChenInstitute of Biological Chemistry, Academia Sinica, 128 Academia Rd., Sec 2, Taipei, 115, Taiwan. 893020260@ndmctsgh.edu.tw.
San SuInstitute of Biological Chemistry, Academia Sinica, 128 Academia Rd., Sec 2, Taipei, 115, Taiwan. susan0702@hotmail.com.
Gen-Der ChenInstitute of Biological Chemistry, Academia Sinica, 128 Academia Rd., Sec 2, Taipei, 115, Taiwan. veranica.g@gmail.com.
Kai-Yun HuangInstitute of Biological Chemistry, Academia Sinica, 128 Academia Rd., Sec 2, Taipei, 115, Taiwan. kai0007tw@gmail.com.
Huang-Wei LienInstitute of Biological Chemistry, Academia Sinica, 128 Academia Rd., Sec 2, Taipei, 115, Taiwan. brian2940@hotmail.com.
Chang-Jen HuangInstitute of Biological Chemistry, Academia Sinica, 128 Academia Rd., Sec 2, Taipei, 115, Taiwan. cjibc@gate.sinica.edu.tw.
Chia-Hsiung ChengDepartment of Biochemistry and Molecular Cell Biology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, 110, Taiwan. chcheng@tmu.edu.tw.
Institute of Biological Chemistry, Academia Sinica · TWTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMutations in mitogen-activated protein kinase (MAPK) kinase 1 (MEK1) that occur during cell proliferation and tumor formation are well described. Information on the roles of MEK2 in these effects is still limited. We established a constitutive MEK2 transgenic zebrafish, Tg(krt14:MEK2S219D-GFP), to elucidate the role of MEK2 in skin tumor formation.

resultsWe found that both constitutive MEK2 and MEK1 are able to phosphorylate the extracellular signal-regulated kinase 1 (ERK1) protein. Transient expression of constitutive MEK2 and MEK1 in the zebrafish epidermis induced papillary formation at 48 h post-fertilization, but no effects were observed due to the expression of MEK1, MEK2, or the dominant negative form of MEK2. The transgenic zebrafish, Tg(krt14:MEK2S219D-GFP), developed skin papillomas in the epidermis within 6 days post-fertilization (dpf). The phospho-ERK signal was detected in section of skin papillomas in an immunohistochemical experiment. Treatment with 50 μM of the MEK inhibitor, U0126, had significantly decreased the skin papilloma formation in Tg(krt14:MEK2S219D-GFP) zebrafish by 6 dpf. In vitro and in vivo proliferation assay in COS-1 cells and in Tg(krt14:MEK2S219D-GFP) transgenic fish show significantly increased cell number and Ki-67 signaling.

conclusionOur data indicate that MEK2 is sufficient to induce epidermal papilloma formation through MAPK signaling in zebrafish, and this transgenic model can be used as a new platform for drug screening.

Indexed as

AnimalsAnimals, Genetically ModifiedEnzyme ActivationMAP Kinase Kinase 2PapillomaSkin NeoplasmsZebrafishZebrafish ProteinsMAP Kinase Kinase 2Zebrafish Proteins

Identifiers

PMID26572230
PMCPMC4647631
OpenAlexW2177551782

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.