Blocking the angiopoietin-2-dependent integrin β-1 signaling axis abrogates small cell lung cancer invasion and metastasis

Meder, Lydia and Orschel, Charlotte Isabelle and Otto, Christoph Julius and Koker, Mirjam and Braegelmann, Johannes and Ercanoglu, Meryem S. and Daehling, Sabrina and Compes, Anik and Selenz, Carolin and Nill, Marieke and Dietlein, Felix and Florin, Alexandra and Eich, Marie-Lisa and Borchmann, Sven and Odenthal, Margarete and Blazquez, Raquel and Hilberg, Frank and Klein, Florian and Hallek, Michael and Buettner, Reinhard and Reinhardt, H. Christian and Ullrich, Roland T. (2024) Blocking the angiopoietin-2-dependent integrin β-1 signaling axis abrogates small cell lung cancer invasion and metastasis. JCI INSIGHT, 9 (10): e166402. ISSN , 2379-3708

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Abstract

Small cell lung cancer (SCLC) is the most aggressive lung cancer entity with an extremely limited therapeutic outcome. Most patients are diagnosed at an extensive stage. However, the molecular mechanisms driving SCLC invasion and metastasis remain largely elusive. We used an autochthonous SCLC mouse model and matched samples from patients with primary and metastatic SCLC to investigate the molecular characteristics of tumor metastasis. We demonstrate that tumor cell invasion and liver metastasis in SCLC are triggered by an Angiopoietin-2 (ANG-2)/ Integrin beta-1-dependent pathway in tumor cells, mediated by focal adhesion kinase/Src kinase signaling. Strikingly, CRISPR-Cas9 KO of Integrin beta-1 or blocking Integrin beta-1 signaling by an anti- ANG-2 treatment abrogates liver metastasis formation in vivo. Interestingly, analysis of a unique collection of matched samples from patients with primary and metastatic SCLC confirmed a strong increase of Integrin beta-1 in liver metastasis in comparison with the primary tumor. We further show that ANG-2 blockade combined with PD-1-targeted by anti -PD -1 treatment displays synergistic treatment effects in SCLC. Together, our data demonstrate a fundamental role of ANG-2/Integrin beta-1 signaling in SCLC cells for tumor cell invasion and liver metastasis and provide a potentially new effective treatment strategy for patients with SCLC.

Item Type: Article
Uncontrolled Keywords: POOR PROGNOSTIC-FACTOR; EXPRESSION; BETA-1-INTEGRIN; INDUCTION; GROWTH;
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Innere Medizin III (Hämatologie und Internistische Onkologie)
Depositing User: Dr. Gernot Deinzer
Date Deposited: 20 Aug 2025 07:48
Last Modified: 20 Aug 2025 07:48
URI: https://pred.uni-regensburg.de/id/eprint/65574

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