U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination
    • Showing Current items.

    WIPF1 WAS/WASL interacting protein family member 1 [ Homo sapiens (human) ]

    Gene ID: 7456, updated on 3-Apr-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    DNA Methylation-Mediated Modulation of Endocytosis as Potential Mechanism for Synaptic Function Regulation in Murine Inhibitory Cortical Interneurons.

    DNA Methylation-Mediated Modulation of Endocytosis as Potential Mechanism for Synaptic Function Regulation in Murine Inhibitory Cortical Interneurons.
    Pensold D, Reichard J, Van Loo KMJ, Ciganok N, Hahn A, Bayer C, Liebmann L, Groß J, Tittelmeier J, Lingner T, Salinas-Riester G, Symmank J, Halfmann C, González-Bermúdez L, Urbach A, Gehrmann J, Costa I, Pieler T, Hübner CA, Vatter H, Kampa B, Becker AJ, Zimmer-Bensch G., Free PMC Article

    12/18/2021
    Crosstalk between WIP and Rho family GTPases.

    Crosstalk between WIP and Rho family GTPases.
    Antón IM, Gómez-Oro C, Rivas S, Wandosell F., Free PMC Article

    07/17/2021
    PD-L1 promotes tumor growth and progression by activating WIP and beta-catenin signaling pathways and predicts poor prognosis in lung cancer.

    PD-L1 promotes tumor growth and progression by activating WIP and β-catenin signaling pathways and predicts poor prognosis in lung cancer.
    Yu W, Hua Y, Qiu H, Hao J, Zou K, Li Z, Hu S, Guo P, Chen M, Sui S, Xiong Y, Li F, Lu J, Guo W, Luo G, Deng W., Free PMC Article

    03/27/2021
    The Disordered Cellular Multi-Tasker WIP and Its Protein-Protein Interactions: A Structural View.

    The Disordered Cellular Multi-Tasker WIP and Its Protein-Protein Interactions: A Structural View.
    Sokolik CG, Qassem N, Chill JH., Free PMC Article

    02/13/2021
    Authors identified WIPF1 as an oncoprotein in PDAC and a direct target of miR-141/miR-200c. They also defined the miR-141/200c-WIPF1-YAP/TAZ as a novel signaling pathway that is involved in the regulation of the invasion and metastasis of human PDAC cells.

    WIPF1 antagonizes the tumor suppressive effect of miR-141/200c and is associated with poor survival in patients with PDAC.
    Pan Y, Lu F, Xiong P, Pan M, Zhang Z, Lin X, Pan M, Huang H., Free PMC Article

    03/30/2019
    WIP deficiency should be considered as a cause for autosomal-recessive immunodeficiency

    Hematopoietic stem cell transplantation corrects WIP deficiency.
    Al-Mousa H, Hawwari A, Al-Ghonaium A, Al-Saud B, Al-Dhekri H, Al-Muhsen S, Elshorbagi S, Dasouki M, El-Baik L, Alseraihy A, Ayas M, Arnaout R.

    12/22/2018
    WIP residues 454-456 are the major contributor to WASp affinity, and residues 449-451 were found to have the largest effect upon WASp ubiquitylation and, presumably, degradation.

    New Structural Insights into Formation of the Key Actin Regulating WIP-WASp Complex Determined by NMR and Molecular Imaging.
    Halle-Bikovski A, Fried S, Rozentur-Shkop E, Biber G, Shaked H, Joseph N, Barda-Saad M, Chill JH.

    05/5/2018
    the present study identifies the WIPF1 gene as having novel oncogenic functions and playing an important role in the invasiveness and aggressiveness of thyroid cancer when aberrantly up-regulated by the BRAF V600E/MAPK pathway through its promoter demethylation.

    Epigenetically upregulated WIPF1 plays a major role in BRAF V600E-promoted papillary thyroid cancer aggressiveness.
    Zhang T, Shen X, Liu R, Zhu G, Bishop J, Xing M., Free PMC Article

    03/10/2018
    WIP controls tumor growth by boosting signals that stabilize the YAP/TAZ complex via a mechanism mediated by the endocytic/endosomal system.

    WIP Drives Tumor Progression through YAP/TAZ-Dependent Autonomous Cell Growth.
    Gargini R, Escoll M, García E, García-Escudero R, Wandosell F, Antón IM.

    11/25/2017
    Results suggest that local invasiveness of ameloblastoma is dependent upon the migratory potential of its tumour cells as defined by their distribution of cortactin, N-WASP and WIP in correlation with F-actin cytoskeletal dynamics.

    Invadopodia proteins, cortactin, N-WASP and WIP differentially promote local invasiveness in ameloblastoma.
    Siar CH, Rahman ZA, Tsujigiwa H, Mohamed Om Alblazi K, Nagatsuka H, Ng KH.

    09/23/2017
    establish a new cancer stem cell signalling pathway downstream of mtp53 in which AKT2 regulates WIP and controls YAP/TAZ stability.

    Mutant p53 oncogenic functions in cancer stem cells are regulated by WIP through YAP/TAZ.
    Escoll M, Gargini R, Cuadrado A, Anton IM, Wandosell F.

    09/16/2017
    Knocking down WIP expression in A549 cells significantly reduced RhoA levels and WIP was found to interact with RhoA suggesting that WIP might be executing its function by regulating RhoA.

    WIP promotes in-vitro invasion ability, anchorage independent growth and EMT progression of A549 lung adenocarcinoma cells by regulating RhoA levels.
    Salvi A, Thanabalu T.

    06/10/2017
    Study provides evidence that WIP and WIRE contribute to breast cancer cell invasiveness through coordinated roles. WIP seems necessary for the assembly of invasive protrusions, whereas WIRE regulates their maturation, which leads to matrix degradation.

    WIP and WICH/WIRE co-ordinately control invadopodium formation and maturation in human breast cancer cell invasion.
    García E, Ragazzini C, Yu X, Cuesta-García E, Bernardino de la Serna J, Zech T, Sarrió D, Machesky LM, Antón IM., Free PMC Article

    02/4/2017
    conclude that tyrosine phosphorylation of WIP is a crucial regulator of WASP stability and function as an actin-nucleation-promoting factor

    Tyrosine phosphorylation of WIP releases bound WASP and impairs podosome assembly in macrophages.
    Vijayakumar V, Monypenny J, Chen XJ, Machesky LM, Lilla S, Thrasher AJ, Antón IM, Calle Y, Jones GE., Free PMC Article

    03/5/2016
    WIP was shown to interact with various binding partners, including the signaling proteins Nck, CrkL and cortactin.

    WIP remodeling actin behind the scenes: how WIP reshapes immune and other functions.
    Noy E, Fried S, Matalon O, Barda-Saad M., Free PMC Article

    08/15/2015
    Data indicate the WASp-interacting protein (WIP)-Wiskott-Aldrich syndrome protein (WASp) interaction in the regulation of actin-dependent processes.

    Triple-color FRET analysis reveals conformational changes in the WIP-WASp actin-regulating complex.
    Fried S, Reicher B, Pauker MH, Eliyahu S, Matalon O, Noy E, Chill J, Barda-Saad M.

    02/21/2015
    These findings reveal WIP as a previously unreported regulator of neuronal maturation and synaptic activity

    WIP is a negative regulator of neuronal maturation and synaptic activity.
    Franco A, Knafo S, Banon-Rodriguez I, Merino-Serrais P, Fernaud-Espinosa I, Nieto M, Garrido JJ, Esteban JA, Wandosell F, Anton IM.

    08/11/2012
    These findings indicate that WIP deficiency should be suspected in patients with features of WAS in whom WAS sequence and mRNA levels are normal.

    A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP.
    Lanzi G, Moratto D, Vairo D, Masneri S, Delmonte O, Paganini T, Parolini S, Tabellini G, Mazza C, Savoldi G, Montin D, Martino S, Tovo P, Pessach IM, Massaad MJ, Ramesh N, Porta F, Plebani A, Notarangelo LD, Geha RS, Giliani S., Free PMC Article

    04/14/2012
    The results suggest that some of the mutations in the WH1 domain cause the Wiskott-Aldrich syndrome syndrome in humans by perturbing the WASP-WIP complex formation.

    Characterization of Wiskott-Aldrich syndrome (WAS) mutants using Saccharomyces cerevisiae.
    Rajmohan R, Raodah A, Wong MH, Thanabalu T.

    02/22/2010
    Groups of colorectal cancer, breast cancer, and glioma patients with low expression of the WIPF1 co-expression module generally had a favorable prognosis.

    An expression module of WIPF1-coexpressed genes identifies patients with favorable prognosis in three tumor types.
    Staub E, Groene J, Heinze M, Mennerich D, Roepcke S, Klaman I, Hinzmann B, Castanos-Velez E, Pilarsky C, Mann B, Brümmendorf T, Weber B, Buhr HJ, Rosenthal A., Free PMC Article

    01/21/2010
    formin-binding protein 17 (FBP17) recruits WASP, WASP-interacting protein (WIP), and dynamin-2 to the plasma membrane and that this recruitment is necessary for the formation of podosomes and phagocytic cups.

    FBP17 Mediates a Common Molecular Step in the Formation of Podosomes and Phagocytic Cups in Macrophages.
    Tsuboi S, Takada H, Hara T, Mochizuki N, Funyu T, Saitoh H, Terayama Y, Yamaya K, Ohyama C, Nonoyama S, Ochs HD., Free PMC Article

    01/21/2010
    WIP is involved in lytic granule transport and is essential for regulation of Natural killer cell cytotoxic function

    WIP is essential for lytic granule polarization and NK cell cytotoxicity.
    Krzewski K, Chen X, Strominger JL., Free PMC Article

    01/21/2010
    that WASP and WASP-interacting protein (WIP) form a complex at the phagocytic cup and that the WASP.WIP complex plays a critical role in the phagocytic cup formation.

    Wiskott-Aldrich syndrome protein is a key regulator of the phagocytic cup formation in macrophages.
    Tsuboi S, Meerloo J.

    01/21/2010
    In this review, in addition to its WASP-independent functions, the role of WIP is to regulate the activity and stability of WASP and shuttle WASP to areas of actin assembly.

    WASP-interacting protein (WIP): working in polymerisation and much more.
    Antón IM, Jones GE, Wandosell F, Geha R, Ramesh N.

    01/21/2010
    the WIP-WASP complex plays an important role in WASP stabilization and NFAT activation

    Structure-function analysis of the WIP role in T cell receptor-stimulated NFAT activation: evidence that WIP-WASP dissociation is not required and that the WIP NH2 terminus is inhibitory.
    Dong X, Patino-Lopez G, Candotti F, Shaw S., Free PMC Article

    01/21/2010
    firstprevious page of 2 nextlast