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YAP nuclear translocation through dynein and acetylated microtubule controls fibroblast activation

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/hep.24485openalex-snapshot
Tumor-secreted lysophostatidic acid accelerates hepatocellular carcinoma progression by promoting differentiation of peritumoral fibroblasts in myofibroblasts
inferredcites →https://doi.org/10.1002/hep.27320openalex-snapshot
Lysyl oxidase-like 2 is critical to tumor microenvironment and metastatic niche formation in hepatocellular carcinoma
inferredcites →https://doi.org/10.1002/jcp.27600openalex-snapshot
Downregulation of SPIN90 promotes fibroblast activation via periostin‐FAK‐ROCK signaling module
inferredcites →https://doi.org/10.1002/path.1427openalex-snapshot
The myofibroblast in wound healing and fibrocontractive diseases
inferredcites →https://doi.org/10.1016/j.addr.2007.08.006openalex-snapshot
Fibroblast mechanics in 3D collagen matrices☆
inferredcites →https://doi.org/10.1016/j.ajpath.2015.08.011openalex-snapshot
YAP1 Is a Driver of Myofibroblast Differentiation in Normal and Diseased Fibroblasts
inferredcites →https://doi.org/10.1016/j.bbrc.2018.04.205openalex-snapshot
Spindle pole body component 25 homolog expressed by ECM stiffening is required for lung cancer cell proliferation
inferredcites →https://doi.org/10.1016/j.ccr.2005.05.024openalex-snapshot
Therapeutic targeting of the tumor microenvironment
inferredcites →https://doi.org/10.1016/j.cell.2006.03.044openalex-snapshot
PPM1A Functions as a Smad Phosphatase to Terminate TGFβ Signaling
inferredcites →https://doi.org/10.1016/j.cell.2006.06.044openalex-snapshot
Matrix Elasticity Directs Stem Cell Lineage Specification
inferredcites →https://doi.org/10.1016/j.cell.2017.10.008openalex-snapshot
Force Triggers YAP Nuclear Entry by Regulating Transport across Nuclear Pores
inferredcites →https://doi.org/10.1016/j.cellsig.2008.12.004openalex-snapshot
Tubulin acetylation favors Hsp90 recruitment to microtubules and stimulates the signaling function of the Hsp90 clients Akt/PKB and p53
inferredcites →https://doi.org/10.1016/j.chom.2009.11.006openalex-snapshot
Adenovirus Transport via Direct Interaction of Cytoplasmic Dynein with the Viral Capsid Hexon Subunit
inferredcites →https://doi.org/10.1016/j.cub.2006.09.014openalex-snapshot
Microtubule Acetylation Promotes Kinesin-1 Binding and Transport
inferredcites →https://doi.org/10.1016/j.jhep.2015.04.011openalex-snapshot
The Hippo pathway effector YAP controls mouse hepatic stellate cell activation
inferredcites →https://doi.org/10.1038/nature02006openalex-snapshot
Smad-dependent and Smad-independent pathways in TGF-β family signalling
inferredcites →https://doi.org/10.1038/ncb2756openalex-snapshot
Mechanotransduction and YAP-dependent matrix remodelling is required for the generation and maintenance of cancer-associated fibroblasts
inferredcites →https://doi.org/10.1038/ncb2777openalex-snapshot
YAP forces fibroblasts to feel the tension
inferredcites →https://doi.org/10.1038/ncomms13817openalex-snapshot
Hepcidin inhibits Smad3 phosphorylation in hepatic stellate cells by impeding ferroportin-mediated regulation of Akt
inferredcites →https://doi.org/10.1038/nrc1586openalex-snapshot
Immunosuppressive networks in the tumour environment and their therapeutic relevance
inferredcites →https://doi.org/10.1038/nrm809openalex-snapshot
Myofibroblasts and mechano-regulation of connective tissue remodelling
inferredcites →https://doi.org/10.1038/onc.2009.299openalex-snapshot
Matrix density-induced mechanoregulation of breast cell phenotype, signaling and gene expression through a FAK–ERK linkage
inferredcites →https://doi.org/10.1038/s41467-018-04121-yopenalex-snapshot
TAK1 activation of alpha-TAT1 and microtubule hyperacetylation control AKT signaling and cell growth
inferredcites →https://doi.org/10.1038/s41598-017-01116-5openalex-snapshot
Transforming growth factor β plays an important role in enhancing wound healing by topical application of Povidone-iodine
inferredcites →https://doi.org/10.1038/s41598-017-07126-7openalex-snapshot
DDR2 controls the epithelial-mesenchymal-transition-related gene expression via c-Myb acetylation upon matrix stiffening
inferredcites →https://doi.org/10.1038/sj.emboj.7601421openalex-snapshot
Snail activation disrupts tissue homeostasis and induces fibrosis in the adult kidney
inferredcites →https://doi.org/10.1038/sj.jid.5700613openalex-snapshot
Formation and Function of the Myofibroblast during Tissue Repair
inferredcites →https://doi.org/10.1053/j.gastro.2004.09.014openalex-snapshot
Hepatocellular carcinoma in cirrhosis: Incidence and risk factors
inferredcites →https://doi.org/10.1073/pnas.0608030104openalex-snapshot
Microtubule function in fibroblast spreading is modulated according to the tension state of cell–matrix interactions
inferredcites →https://doi.org/10.1074/jbc.274.11.7391openalex-snapshot
Importin β Recognizes Parathyroid Hormone-related Protein with High Affinity and Mediates Its Nuclear Import in the Absence of Importin α
inferredcites →https://doi.org/10.1074/jbc.274.2.918openalex-snapshot
Differences in the Regulation of Fibroblast Contraction of Floating Versus Stressed Collagen Matrices
inferredcites →https://doi.org/10.1074/jbc.m109.075218openalex-snapshot
Force-induced Myofibroblast Differentiation through Collagen Receptors Is Dependent on Mammalian Diaphanous (mDia)
inferredcites →https://doi.org/10.1074/jbc.m115.700823openalex-snapshot
Importin α1 Mediates Yorkie Nuclear Import via an N-terminal Non-canonical Nuclear Localization Signal
inferredcites →https://doi.org/10.1074/jbc.m115.713123openalex-snapshot
Loss of α-Tubulin Acetylation Is Associated with TGF-β-induced Epithelial-Mesenchymal Transition
inferredcites →https://doi.org/10.1083/jcb.121.4.811openalex-snapshot
Differential regulation of tropomyosin isoform organization and gene expression in response to altered actin gene expression.
inferredcites →https://doi.org/10.1083/jcb.139.2.469openalex-snapshot
Overexpression of the Dynamitin (p50) Subunit of the Dynactin Complex Disrupts Dynein-dependent Maintenance of Membrane Organelle Distribution
inferredcites →https://doi.org/10.1091/mbc.12.9.2730openalex-snapshot
Alpha-Smooth Muscle Actin Expression Upregulates Fibroblast Contractile Activity
inferredcites →https://doi.org/10.1093/emboj/16.17.5353openalex-snapshot
TGF‐β receptor‐mediated signalling through Smad2, Smad3 and Smad4
inferredcites →https://doi.org/10.1101/gad.12.11.1587openalex-snapshot
Smad2 transduces common signals from receptor serine–threonine and tyrosine kinases
inferredcites →https://doi.org/10.1101/gad.239327.114openalex-snapshot
Rho-actin signaling to the MRTF coactivators dominates the immediate transcriptional response to serum in fibroblasts
inferredcites →https://doi.org/10.1111/j.1432-1033.1992.tb16875.xopenalex-snapshot
Calponin and SM 22 isoforms in avian and mammalian smooth muscle
inferredcites →https://doi.org/10.1111/j.1600-0854.2007.00564.xopenalex-snapshot
A Microtubule‐Facilitated Nuclear Import Pathway for Cancer Regulatory Proteins
inferredcites →https://doi.org/10.1111/j.1600-0854.2009.00937.xopenalex-snapshot
Importins and Beyond: Non‐Conventional Nuclear Transport Mechanisms
inferredcites →https://doi.org/10.1126/science.aar1968openalex-snapshot
Asymmetric distribution and spatial switching of dynein activity generates ciliary motility
inferredcites →https://doi.org/10.1152/ajplung.00300.2014openalex-snapshot
Mechanosignaling through YAP and TAZ drives fibroblast activation and fibrosis
inferredcites →https://doi.org/10.1152/ajplung.00390.2011openalex-snapshot
Neuronal Wiskott-Aldrich syndrome protein (N-WASP) is critical for formation of α-smooth muscle actin filaments during myofibroblast differentiation
inferredcites →https://doi.org/10.1158/0008-5472.can-17-0657openalex-snapshot
SPIN90 Depletion and Microtubule Acetylation Mediate Stromal Fibroblast Activation in Breast Cancer Progression
inferredcites →https://doi.org/10.1165/rcmb.2012-0050ocopenalex-snapshot
Matrix Stiffness–Induced Myofibroblast Differentiation Is Mediated by Intrinsic Mechanotransduction
inferredcites →https://doi.org/10.1172/jci200524282openalex-snapshot
Liver fibrosis
inferredcites →https://doi.org/10.1172/jci66369openalex-snapshot
Hepatic stellate cells in liver development, regeneration, and cancer
inferredcites →https://doi.org/10.1242/jcs.108886openalex-snapshot
Matrix stiffness reverses the effect of actomyosin tension on cell proliferation
inferredcites →https://doi.org/10.1371/journal.pone.0070196openalex-snapshot
Myofibroblast Differentiation and Enhanced Tgf-B Signaling in Cystic Fibrosis Lung Disease
inferredcites →https://doi.org/10.1371/journal.pone.0074342openalex-snapshot
CK2 Inhibitor CX-4945 Blocks TGF-β1-Induced Epithelial-to-Mesenchymal Transition in A549 Human Lung Adenocarcinoma Cells
inferredcites →https://doi.org/10.1371/journal.pone.0077166openalex-snapshot
Smooth Muscle α Actin (Acta2) and Myofibroblast Function during Hepatic Wound Healing
inferredcites →https://doi.org/10.1371/journal.pone.0135519openalex-snapshot
Extracellular Matrix Stiffness Regulates Osteogenic Differentiation through MAPK Activation
inferredcites →https://doi.org/10.1681/asn.2015050499openalex-snapshot
YAP/TAZ Are Mechanoregulators of TGF-β-Smad Signaling and Renal Fibrogenesis
inferredcites →https://doi.org/10.2353/ajpath.2007.070112openalex-snapshot
The Myofibroblast
inferredcites →https://doi.org/10.2353/ajpath.2009.081170openalex-snapshot
Emerging Concepts in the Pathogenesis of Lung Fibrosis
inferredcites →https://doi.org/10.7554/elife.21768openalex-snapshot
Lissencephaly-1 is a context-dependent regulator of the human dynein complex

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.jare.2025.08.006openalex-snapshot
Innovative applications of multidimensional engineered hydrogels in wound healing
inferred← citeshttps://doi.org/10.3390/biomedicines8090338openalex-snapshot
Potent Small-Molecule Inhibitors Targeting Acetylated Microtubules as Anticancer Agents Against Triple-Negative Breast Cancer
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