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Chitinase-like proteins promoting tumorigenesis through disruption of cell polarity via enlarged endosomal vesicles
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för molekylär biovetenskap, Wenner-Grens institut.ORCID-id: 0000-0002-9785-9641
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för molekylär biovetenskap, Wenner-Grens institut.ORCID-id: 0000-0001-5297-2846
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för molekylär biovetenskap, Wenner-Grens institut.
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för molekylär biovetenskap, Wenner-Grens institut.
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Rekke forfattare: 52023 (engelsk)Inngår i: Frontiers in Oncology, E-ISSN 2234-943X, Vol. 13, artikkel-id 1170122Artikkel i tidsskrift (Fagfellevurdert) 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.

sted, utgiver, år, opplag, sider
2023. Vol. 13, artikkel-id 1170122
Emneord [en]
Drosophila, immunity, tumor, endosomal vesicles, salivary glands, chitinase, insect immunity
HSV kategori
Identifikatorer
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
Tilgjengelig fra: 2023-07-26 Laget: 2023-07-26 Sist oppdatert: 2024-01-17bibliografisk kontrollert

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Khalili, DilanKunc, MartinTheopold, Ulrich

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