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Verfasst von:Machiraju, Devayani [VerfasserIn]   i
 Hassel, Jessica C. [VerfasserIn]   i
Titel:Targeting the cMET pathway to enhance immunotherapeutic approaches for mUM patients
Verf.angabe:Devayani Machiraju and Jessica C. Hassel
E-Jahr:2023
Jahr:24 January 2023
Umfang:7 S.
Fussnoten:Gesehen am 06.02.2023
Titel Quelle:Enthalten in: Frontiers in oncology
Ort Quelle:Lausanne : Frontiers Media, 2011
Jahr Quelle:2023
Band/Heft Quelle:12(2023) vom: Jan., Artikel-ID 1068029, Seite 1-7
ISSN Quelle:2234-943X
Abstract:The liver is the most preferential initial site of metastasis for uveal melanoma (mUM), and this preference is associated with rapid mortality in mUM patients. Despite the significant clinical benefits of Immune checkpoint inhibitors (ICIs) in metastatic cutaneous melanoma patients, ICIs have shown little to no benefit in mUM patients. A potential reason for this inefficiency of ICI could be partly devoted to the involvement of the liver itself, thanks to its rich source of growth factors and immunosuppressive microenvironment. Uveal melanoma cells show increased expression of a transmembrane protein called cMET, which is known as the sole receptor for the Hepatocyte growth factor (HGF). Hyperactivation of cMET by HGF contributes to mUM development, and the liver, being the major source of HGF, may partially explain the metastasis of uveal melanoma cells to the liver. In addition, cMET/HGF signaling has also been shown to mediate resistance to ICI treatment, directly and indirectly, involving tumor and immune cell populations. Therefore, targeting the cMET/HGF interaction may enhance the efficacy of immunotherapeutic regimes for mUM patients. Hence in this minireview, we will discuss the rationale for combining cMET inhibitors/antibodies with leading immune checkpoint inhibitors for treating mUM. We will also briefly highlight the challenges and opportunities in targeting cMET in mUM.
DOI:doi:10.3389/fonc.2022.1068029
URL:kostenfrei: Volltext: https://doi.org/10.3389/fonc.2022.1068029
 kostenfrei: Volltext: https://www.frontiersin.org/articles/10.3389/fonc.2022.1068029
 DOI: https://doi.org/10.3389/fonc.2022.1068029
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1833277406
Verknüpfungen:→ Zeitschrift
 
 
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