Evidence map›Paper›PMID 29366443›Full record

ReviewBMB reports2018

Hippo-YAP/TAZ signaling in angiogenesis.

Jeong Ae Park, Young-Guen Kwon

Abstract readReview
In one paragraph

Review in BMB reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Article
  2. Article
  3. Endothelial UNC5B regulates blood‑retinal barrier homeostasis.International journal of molecular medicine · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. YAP/STAT3 inhibited CD8Cancer medicine · 2023
    Article
  15. Article
  16. Article
  17. The Hippo Signaling Pathway as a Drug Target in Familial Dilated Cardiomyopathy.International journal of drug discovery and pharmacology · 2022
    Article
  18. Identification of a novel LATS1 variant associated with familial cerebral cavernous malformations in a Chinese family.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  19. Article
  20. Overexpression ofZoological research · 2022
    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

2 authors.

Jeong Ae ParkDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University; Initiative for Biological Function & Systems, BK21 PLUS, Yonsei University, Seoul 03722, Korea.
Young-Guen KwonDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University; Initiative for Biological Function & Systems, BK21 PLUS, Yonsei University, Seoul 03722, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiogenesis is a complex, multistep process involving dynamic changes in endothelial cell (EC) shapes and behaviors, especially in specialized cell types such as tip cells (with active filopodial extensions), stalk cells (with less motility) and phalanx cells (with stable junction connections). The Hippo-Yes-associated protein (YAP)/ transcription activator with PDZ binding motif (TAZ) signaling plays a critical role in development, regeneration and organ size by regulating cell-cell contact and actin cytoskeleton dynamics. Recently, with the finding that YAP is expressed in the front edge of the developing retinal vessels, Hippo-YAP/TAZ signaling has emerged as a new pathway for blood vessel development. Intriguingly, the LATS1/2-mediated angiomotin (AMOT) family and YAP/TAZ activities contribute to EC shapes and behaviors by spatiotemporally modulating actin cytoskeleton dynamics and EC junction stability. Herein, we summarize the recent understanding of the role of Hippo-YAP/TAZ signaling in the processes of EC sprouting and junction maturation in angiogenesis. [BMB Reports 2018; 51(3): 157-162].

Indexed as

AcyltransferasesAnimalsCell Cycle ProteinsHippo Signaling PathwayHumansNeovascularization, PathologicNuclear ProteinsProtein Serine-Threonine KinasesSignal TransductionTranscription FactorsTumor Suppressor ProteinsAcyltransferasesCell Cycle ProteinsLATS1 protein, humanLATS2 protein, humanNuclear ProteinsProtein Serine-Threonine KinasesTAFAZZIN protein, humanTranscription FactorsTumor Suppressor ProteinsYY1AP1 protein, human

Identifiers

PMID29366443
PMCPMC5882223

What OpenQuestion holds

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Registered trials

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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.