Cited by 112Hippo pathway signaling and YAP/TAZAngiogenesis and VEGF in CancerMechanisms of cancer metastasis

The Angiomotins – From discovery to function

Open access
Moleirinho, Susana, Guerrant, William, Kissil, Joseph L.·2014·FEBS Letters

Abstract

Angiomotins were originally identified as angiostatin binding proteins and implicated in the regulation of endothelial cell migration. Recent studies have shed light on the role of Angiomotins and other members of the Motin protein family in epithelial cells and in pathways directly linked to the pathogenesis of cancer. In particular, Motins have been shown to play a role in signaling pathways regulated by small G‐proteins and the Hippo–YAP pathway. In this review the role of the Motin protein family in these signaling pathways will be described and open questions will be discussed.

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Crossref · 10.1016/j.febslet.2014.02.006

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  • Bag3 regulates Yap and Taz activity by binding to Yap and Taz binding partners such as Lats1, Amotl1 and Amotl2.

    “Additionally, Bag3 regulates Yap and Taz activity by binding to Yap and Taz binding partners, such as the Hippo kinase Lats1, Amotl1 and Amotl2 (reviewed in (102)).”

    From The Hippo signal transduction network for exercise physiologists (2016) · cites this paper as [102]

    The ‘Function: Angiomotin regulation of Hpo/YAP signaling’ section (page unavailable) describes AmotL1, AmotL2 and LATS1/2 as YAP binding partners and discusses angiomotin regulation of YAP/TAZ. It does not establish the claim’s central mechanism—that Bag3 binds LATS1, AmotL1 or AmotL2 to regulate YAP/TAZ—and a search for BAG3 found no relevant passage. (LLM, conf=0.85)

    Experimental — accuracy not yet measured

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References 98 · Cited by 112

Research works printed but not linked: 1

  1. [86]Zhao B Inactivation of YAP oncoprotein by the Hippo pathway is involved in cell contact inhibition and tissue growth control. Genes & development 2007 21 2747 61 17974916 PMC2045129

Authors
Moleirinho, S., Guerrant, W., & Kissil, J. L.
Affiliations
Scripps Research Institute (US)
Corresponding author
Kissil, Joseph L.
Venue
FEBS Letters
Publisher
Wiley
Published
2014-02-15
Volume
588
Issue
16
Pages
2693-2703
ISSN
  • 0014-5793 (ISSN-L)
  • 1873-3468
OpenAlex
W2038411007
Cited by
112
References
98
Citations by year
2026: 2 · 2025: 5 · 2024: 6 · 2023: 4 · 2022: 7 · 2021: 13 · 2020: 6 · 2019: 11 · 2018: 10 · 2017: 14 · 2016: 14 · 2015: 12 · 2014: 8
FWCI
1.60
Type
journal article
Language
en
Open access
Locations
  • FEBS Letters (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Cancer Institute (R01CA124495)
  • National Institute of Neurological Disorders and Stroke (R01NS077952)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Hippo pathway signaling and YAP/TAZ
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mechanisms of cancer metastasis
Keywords
angiomotin, endothelial cell migration, epithelial cells, small GTPases, Hippo-YAP signaling pathway, carcinogenesis
MeSH terms
Angiomotins, Animals, Disease, Gene Expression Regulation, Humans, Membrane Proteins, Microfilament Proteins, Signal Transduction, Neovascularization, Physiologic, Intercellular Signaling Peptides and Proteins, Endothelial Cells

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