Evidence map›Paper›PMID 22003437›Full record

ArticleInternational journal of biochemistry and molecular biology2011

Regulation and function of the TAZ transcription co-activator.

Chenying Liu, Wei Huang, Qunying Lei

Open access · greenAbstract read
In one paragraph

Article in International journal of biochemistry and molecular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  12. A role for the transducer of the Hippo pathway, TAZ, in the development of aggressive types of endometrial cancer.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2015
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  13. Article
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  16. WWTR1 (WW domain containing transcription regulator 1).Atlas of genetics and cytogenetics in oncology and haematology · 2014
    Article
  17. Article
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  19. 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

3 authors.

Chenying Liu
Wei Huang
Qunying Lei

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TAZ (WWTR1), identified as a 14-3-3 binding protein with a PDZ binding motif, is implicated in mesenchymal stem cell differentiation. TAZ has been shown to be negatively regulated by phosphorylation-dependent and phosphorylation-independent mechanisms. Coupled with ASPP2, PP1 dephosphorylates TAZ to activate TAZ. TEADs mediate TAZ function in promoting cell proliferation and epithelial-mesenchymal transition (EMT). TAZ senses different cellular signals such as cell density and the extracellular matrix stiffness. Significantly, TAZ is overexpressed in breast cancer samples and papillary thyroid carcinoma tissues. These results indicate that TAZ plays an important role in cancer development and presents a novel target for TAZ overexpressed cancer therapy.

Indexed as

14-3-3 binding proteinepithelial-mesenchymal transition (EMT)PDZ binding motifsignal transductionstem cellTAZ (WWTR1)

Identifiers

PMID22003437
PMCPMC3193294
OpenAlexW2291767161

What OpenQuestion holds

Textmetadata
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.