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Status: Bibliographieeintrag

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Verfasst von:Sun, Yifeng [VerfasserIn]   i
 Qiao, Yina [VerfasserIn]   i
 Niu, Yiqi [VerfasserIn]   i
 Madhavan, Bindhu Kollivayal [VerfasserIn]   i
 Fang, Chao [VerfasserIn]   i
 Hu, Jingxiong [VerfasserIn]   i
 Schuck, Kathleen [VerfasserIn]   i
 Traub, Benno [VerfasserIn]   i
 Friess, Helmut [VerfasserIn]   i
 Herr, Ingrid [VerfasserIn]   i
 Michalski, Christoph [VerfasserIn]   i
 Kong, Bo [VerfasserIn]   i
Titel:ARP2/3 complex affects myofibroblast differentiation and migration in pancreatic ductal adenocarcinoma
Verf.angabe:Yifeng Sun, Yina Qiao, Yiqi Niu, Bindhu Kollivayal Madhavan, Chao Fang, Jingxiong Hu, Kathleen Schuck, Benno Traub, Helmut Friess, Ingrid Herr, Christoph W. Michalski, Bo Kong
E-Jahr:2025
Jahr:29 October 2024
Umfang:10 S.
Fussnoten:Gesehen am 16.05.2025
Titel Quelle:Enthalten in: International journal of cancer
Ort Quelle:Bognor Regis : Wiley-Liss, 1966
Jahr Quelle:2025
Band/Heft Quelle:156(2025), 6, Seite 1272-1281
ISSN Quelle:1097-0215
Abstract:The ARP2/3 complex, which orchestrates actin cytoskeleton organization and lamellipodia formation, has been implicated in the initiation of pancreatic ductal adenocarcinoma (PDAC). This study aims to clarify its impact on the activity of cancer-associated fibroblasts (CAFs), key players in PDAC progression, and patient outcomes. Early pancreatic carcinogenesis was modeled in p48Cre; LSL-KrasG12D mice with caerulein-induced pancreatitis, complemented by in vitro studies on human immortalized pancreatic stellate cells (PSCs) and primary PDAC-derived CAFs. Data were gained from microarray analysis, RNA sequencing (RNA-seq), and single-cell RNA sequencing (sc-RNA-seq), with subsequent bioinformatics analysis. We uncovered a specific transcriptional signature associated with fibroblast migration in early pancreatic carcinogenesis and linked it to poor survival in patients with PDAC. A pivotal role of the ARP2/3 complex in CAF migration was identified. Inhibition of the ARP2/3 complex markedly decreased CAF motility and induced significant morphological changes in vitro. Furthermore, its inhibition also hindered TGFβ1-mediated myofibroblastic CAF differentiation but had no effect on IL-1-mediated inflammatory CAF differentiation. Our findings position the ARP2/3 complex as central to the migration and differentiation of myofibroblastic CAF. Targeting this complex presents a promising new therapeutic avenue for PDAC treatment.
DOI:doi:10.1002/ijc.35246
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.1002/ijc.35246
 kostenfrei: Volltext: https://onlinelibrary.wiley.com/doi/10.1002/ijc.35246
 DOI: https://doi.org/10.1002/ijc.35246
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Actin-Related Protein 2-3 Complex
 Animals
 Cancer-Associated Fibroblasts
 cancer‐associated fibroblasts
 Carcinogenesis
 Carcinoma, Pancreatic Ductal
 Cell Movement
 Ceruletide
 Gene Expression Profiling
 Humans
 Mice
 myCAFs
 Myofibroblasts
 pancreatic carcinogenesis
 Pancreatic Stellate Cells
 Prognosis
 transcriptional signature
 transforming growth factor β
 Tumor Microenvironment
K10plus-PPN:1925852148
Verknüpfungen:→ Zeitschrift

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