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LASP1 in cellular signaling and gene expression: more than just a cytoskeletal regulator

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-297447
  • LIM and SH3 protein 1 was originally identified as a structural cytoskeletal protein with scaffolding function. However, recent data suggest additional roles in cell signaling and gene expression, especially in tumor cells. These novel functions are primarily regulated by the site-specific phosphorylation of LASP1. This review will focus on specific phosphorylation-dependent interaction between LASP1 and cellular proteins that orchestrate primary tumor progression and metastasis. More specifically, we will describe the role of LASP1 inLIM and SH3 protein 1 was originally identified as a structural cytoskeletal protein with scaffolding function. However, recent data suggest additional roles in cell signaling and gene expression, especially in tumor cells. These novel functions are primarily regulated by the site-specific phosphorylation of LASP1. This review will focus on specific phosphorylation-dependent interaction between LASP1 and cellular proteins that orchestrate primary tumor progression and metastasis. More specifically, we will describe the role of LASP1 in chemokine receptor, and PI3K/AKT signaling. We outline the nuclear role for LASP1 in terms of epigenetics and transcriptional regulation and modulation of oncogenic mRNA translation. Finally, newly identified roles for the cytoskeletal function of LASP1 next to its known canonical F-actin binding properties are included.zeige mehrzeige weniger

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Metadaten
Autor(en): Elke Butt, Cory M. Howard, Dayanidhi Raman
URN:urn:nbn:de:bvb:20-opus-297447
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Institut für Experimentelle Biomedizin
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Cells
ISSN:2073-4409
Erscheinungsjahr:2022
Band / Jahrgang:11
Heft / Ausgabe:23
Aufsatznummer:3817
Originalveröffentlichung / Quelle:Cells (2022) 11:23, 3817. https://doi.org/10.3390/cells11233817
DOI:https://doi.org/10.3390/cells11233817
Allgemeine fachliche Zuordnung (DDC-Klassifikation):5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Freie Schlagwort(e):AKT; CXCR4; LASP1; cytoskeleton; epigenetics; nucleus; phosphorylation; structure; transcriptional regulation
Datum der Freischaltung:16.10.2023
Datum der Erstveröffentlichung:29.11.2022
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International