Evidence map›Paper›PMID 28279208›Full record

ReviewChinese journal of cancer2017

Corepressor metastasis-associated protein 3 modulates epithelial-to-mesenchymal transition and metastasis.

Liang Du, Zhifeng Ning, Hao Zhang, Fuxing Liu

Abstract readReview
In one paragraph

Review in Chinese journal of cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
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  5. Review
  6. Article
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  11. Article
  12. Article
  13. Cancer metastasis: issues and challenges.Chinese journal of cancer · 2017
    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

4 authors.

Liang DuCancer Research Center, Shantou University Medical College, Shantou, 515031, Guangdong, P. R. China.
Zhifeng NingBasic Medicine College, Hubei University of Science and Technology, Xianning, 437100, Hubei, P. R. China.
Hao ZhangCancer Research Center, Shantou University Medical College, Shantou, 515031, Guangdong, P. R. China. haozhang@stu.edu.cn.
Fuxing LiuBasic Medicine College, Hubei University of Science and Technology, Xianning, 437100, Hubei, P. R. China. liufx6505@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Worldwide, metastasis is the leading cause of more than 90% of cancer-related deaths. Currently, no specific therapies effectively impede metastasis. Metastatic processes are controlled by complex regulatory networks and transcriptional hierarchy. Corepressor metastasis-associated protein 3 (MTA3) has been confirmed as a novel component of nucleosome remodeling and histone deacetylation (NuRD). Increasing evidence supports the theory that, in the recruitment of transcription factors, coregulators function as master regulators rather than passive passengers. As a master regulator, MTA3 governs the target selection for NuRD and functions as a transcriptional repressor. MTA3 dysregulation is associated with tumor progression, invasion, and metastasis in various cancers. MTA3 is also a key regulator of E-cadherin expression and epithelial-to-mesenchymal transition. Elucidating the functions of MTA3 might help to find additional therapeutic approaches for targeting components of NuRD.

Indexed as

Epithelial-Mesenchymal TransitionAnimalsCo-Repressor ProteinsHumansNeoplasm MetastasisNeoplasm ProteinsNeoplasmsCo-Repressor ProteinsMTA3 protein, humanNeoplasm ProteinsCoregulatorMaster regulatorMetastasis associated proteinsNuRD complex

Identifiers

PMID28279208
PMCPMC5345190

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.