| Literature DB >> 29759564 |
Benoîte Mery1, Sophie Espenel2, Jean-Baptiste Guy2, Chloé Rancoule2, Alexis Vallard2, Marie-Thérèse Aloy3, Claire Rodriguez-Lafrasse3, Nicolas Magné2.
Abstract
Chondrosarcomas are characterized by their chemo- and radioresistance leading to a therapeutic surgical approach which remains the only available treatment with a 10-year survival between 30% and 80% depending on the grade. Non-surgical treatments are under investigation and rely on an accurate biological understanding of drug resistance mechanisms. Novel targeted therapy which represents a new relevant therapeutic approach will open new treatment options by targeting several pathways responsible for processes of proliferation and invasion. Survival pathways such as PI3K, AKT, mTOR and VEGF have been shown to be involved in proliferation of chondrosarcoma cells and antiapoptotic proteins may also play a relevant role. Other proteins such as p53 or COX2 have been identified as potential new targets. This review provides an insight into the biological substantial treatment challenges of CHS and focuses on improving our understanding of CH biology through an overview of major signaling pathways that could represent targets for new therapeutic approaches.Entities:
Keywords: Biology; Chemo and radiation resistance; Chondrosarcoma; Signaling pathways
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Year: 2018 PMID: 29759564 DOI: 10.1016/j.critrevonc.2018.03.009
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312