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Chitinase-like proteins promoting tumorigenesis through disruption of cell polarity via enlarged endosomal vesicles
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.ORCID iD: 0000-0002-9785-9641
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.ORCID iD: 0000-0001-5297-2846
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
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Number of Authors: 52023 (English)In: Frontiers in Oncology, E-ISSN 2234-943X, Vol. 13, article id 1170122Article in journal (Refereed) Published
Abstract [en]

Introduction: Chitinase-like proteins (CLPs) are associated with tissue-remodeling and inflammation but also with several disorders, including fibrosis, atherosclerosis, allergies, and cancer. However, CLP’s role in tumors is far from clear.

Methods: Here, we utilize Drosophila melanogaster and molecular genetics to investigate the function of CLPs (imaginal disc growth factors; Idgf’s) in RasV12 dysplastic salivary glands.

Results and discussion: We find one of the Idgf’s members, Idgf3, is transcriptionally induced in a JNK-dependent manner via a positive feedback loop mediated by reactive oxygen species (ROS). Moreover, Idgf3 accumulates in enlarged endosomal vesicles (EnVs) that promote tumor progression by disrupting cytoskeletal organization. The process is mediated via the downstream component, aSpectrin, which localizes to the EnVs. Our data provide new insight into CLP function in tumors and identifies specific targets for tumor control.

Place, publisher, year, edition, pages
2023. Vol. 13, article id 1170122
Keywords [en]
Drosophila, immunity, tumor, endosomal vesicles, salivary glands, chitinase, insect immunity
National Category
Cell and Molecular Biology
Identifiers
URN: urn:nbn:se:su:diva-218037DOI: 10.3389/fonc.2023.1170122ISI: 000986003400001PubMedID: 37188187Scopus ID: 2-s2.0-85159168083OAI: oai:DiVA.org:su-218037DiVA, id: diva2:1784307
Available from: 2023-07-26 Created: 2023-07-26 Last updated: 2024-01-17Bibliographically approved

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Khalili, DilanKunc, MartinTheopold, Ulrich

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