Microenvironment matters: insights from the FOSTER consortium on microenvironment-driven approaches to osteosarcoma therapy

被引:0
|
作者
Aurelie Dutour [1 ]
Michela Pasello [2 ]
Luke Farrow [3 ]
Mahetab H. Amer [4 ]
Natacha Entz-Werlé [5 ]
Michaela Nathrath [6 ]
Katia Scotlandi [7 ]
Sibylle Mittnacht [8 ]
Anne Gomez-Mascard [2 ]
机构
[1] Université Claude Bernard Lyon 1,Childhood Cancer & Cell Death Team, Centre de Recherche en Cancérologie de Lyon (CRCL), Centre Léon Bérard
[2] IRCCS Istituto Ortopedico Rizzoli,Laboratory of Experimental Oncology
[3] University College London Cancer Institute,Division of Cell Matrix & Regenerative Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health
[4] University College London,Pediatric Onco
[5] University of Manchester,Hematology Unit
[6] University Hospitals of Strasbourg,Translational, Transversal and Therapeutic Oncology Team, Laboratory of Bioimaging and Pathologies
[7] Faculty of Pharmacy,Department of Pediatric Hemato
[8] Children’s Hospital Kassel,Oncology, Psychosomatics and Systemic Diseases
[9] Technical University of Munich,Department of Pediatrics, Children’S Cancer Research Center, School of Medicine
[10] University of Toulouse,Department of Pathology, CHU, IUCT
关键词
Tumor microenvironment; Osteosarcoma; Hypoxia; Mesenchymal stroma; Immunotherapy; Therapeutic strategy;
D O I
10.1007/s10555-025-10257-3
中图分类号
学科分类号
摘要
Osteosarcoma (OS), a prevalent malignant bone tumor, has seen limited progress in treatment efficacy and patient outcomes over decades. Recent insights into the tumor microenvironment (TME) have revealed its crucial role in tumor progression and therapeutic resistance, particularly in OS. This review offers a comprehensive exploration of the OS microenvironment, meticulously dissecting its crucial components: the mesenchymal stromal TME, the immune microenvironment, hypoxia-induced adaptations, and the impact of the physical microenvironment. By demonstrating how these elements collectively drive tumor proliferation, immune evasion, and invasion, this review explores the intricate molecular and cellular dynamics at play. Furthermore, innovative approaches targeting the OS microenvironment, such as immunotherapies, are presented. This review highlights the importance of the TME in OS progression and its potential as a source of novel therapeutic strategies, offering new hope for improved patient outcomes.
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