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1000 Titel
  • Drug prioritization identifies panobinostat as a tailored treatment element for patients with metastatic hepatoblastoma
1000 Autor/in
  1. Demir, Salih |
  2. Hotes, Alina |
  3. Schmid, Tanja |
  4. Cairo, Stefano |
  5. Indersie, Emilie |
  6. Pisano, Claudio |
  7. Hiyama, Eiso |
  8. Hishiki, Tomoro |
  9. Vokuhl, Christian |
  10. Branchereau, Sophie |
  11. Brock, Penelope |
  12. Schmid, Irene |
  13. Zsiros, József |
  14. Kappler, Roland |
1000 Verlag BioMed Central
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-11-12
1000 Erschienen in
1000 Quellenangabe
  • 43(1):299
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13046-024-03221-6 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556140/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>Patients with metastatic hepatoblastoma are treated with severely toxic first-line chemotherapies in combination with surgery. Yet, inadequate response of lung metastases to neo-adjuvant chemotherapy still compromises patient outcomes making new treatment strategies, tailored to more efficient lung clearance, mandatory.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>We harnessed a comprehensive patient-derived xenograft platform and a variety of in vitro and in vivo assays to establish the preclinical and biological rationale for a new drug for patients with metastatic hepatoblastoma.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>The testing of a library of established drugs on patient-derived xenografts identified histone deacetylase inhibitors, most notably panobinostat, to be highly efficacious on hepatoblastoma cells, as compared to non-cancerous cells. Molecularly, the anti-tumor effect of panobinostat is mediated by posttranslational obstruction of the MYC oncoprotein as a result of dual specificity phosphatase 1 upregulation, thereby leading to growth inhibition and programmed cell death. Of clinical importance, upregulation of the MYC target gene nucleophosmin 1 is indicative of response to panobinostat and associated with metastatic disease in patients with hepatoblastoma. The combination of panobinostat with the current SIOPEL 4 induction protocol, consisting of cisplatin and doxorubicin, revealed high synergies already at low nanomolar levels. The simulation of a clinical trial, with this combination therapy, in patient-derived xenograft models, and ultimately heterotypic lung metastasis mimics clearly underscored the potency of this approach.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusion</jats:title> <jats:p>Integrated studies define MYC inhibition by panobinostat as a novel treatment element to be introduced into the therapeutic strategy for patients with metastatic hepatoblastoma.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Hepatoblastoma/drug therapy [MeSH]
lokal Histone Deacetylase Inhibitors/therapeutic use [MeSH]
lokal Cell Line, Tumor [MeSH]
lokal Metastasis
lokal Therapy
lokal Antineoplastic Agents/pharmacology [MeSH]
lokal Liver Neoplasms/pathology [MeSH]
lokal Panobinostat
lokal Xenograft Model Antitumor Assays [MeSH]
lokal Hepatoblastoma/metabolism [MeSH]
lokal Female [MeSH]
lokal MYC
lokal Histone Deacetylase Inhibitors/pharmacology [MeSH]
lokal Humans [MeSH]
lokal Animals [MeSH]
lokal Hepatoblastoma/pathology [MeSH]
lokal Antineoplastic Combined Chemotherapy Protocols/therapeutic use [MeSH]
lokal Mice [MeSH]
lokal Antineoplastic Combined Chemotherapy Protocols/pharmacology [MeSH]
lokal Liver Neoplasms/secondary [MeSH]
lokal Research
lokal Antineoplastic Agents/therapeutic use [MeSH]
lokal Lung Neoplasms/pathology [MeSH]
lokal Panobinostat/pharmacology [MeSH]
lokal Lung Neoplasms/drug therapy [MeSH]
lokal Panobinostat/therapeutic use [MeSH]
lokal Hepatoblastoma
lokal Lung Neoplasms/secondary [MeSH]
lokal Liver Neoplasms/drug therapy [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/RGVtaXIsIFNhbGlo|https://frl.publisso.de/adhoc/uri/SG90ZXMsIEFsaW5h|https://frl.publisso.de/adhoc/uri/U2NobWlkLCBUYW5qYQ==|https://frl.publisso.de/adhoc/uri/Q2Fpcm8sIFN0ZWZhbm8=|https://frl.publisso.de/adhoc/uri/SW5kZXJzaWUsIEVtaWxpZQ==|https://frl.publisso.de/adhoc/uri/UGlzYW5vLCBDbGF1ZGlv|https://frl.publisso.de/adhoc/uri/SGl5YW1hLCBFaXNv|https://frl.publisso.de/adhoc/uri/SGlzaGlraSwgVG9tb3Jv|https://frl.publisso.de/adhoc/uri/Vm9rdWhsLCBDaHJpc3RpYW4=|https://frl.publisso.de/adhoc/uri/QnJhbmNoZXJlYXUsIFNvcGhpZQ==|https://frl.publisso.de/adhoc/uri/QnJvY2ssIFBlbmVsb3Bl|https://frl.publisso.de/adhoc/uri/U2NobWlkLCBJcmVuZQ==|https://frl.publisso.de/adhoc/uri/WnNpcm9zLCBKw7N6c2Vm|https://orcid.org/0000-0002-8581-2803
1000 Hinweis
  • DeepGreen-ID: 5c645f770e1d4acc95eb3fca13508348 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
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  1. Klinikum der Universität München |
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1000 Dateien
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    1000 Förderer Klinikum der Universität München |
    1000 Förderprogramm -
    1000 Fördernummer -
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1000 Erstellt am 2025-07-04T07:05:52.202+0200
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1000 Objekt bearb. Fri Aug 15 19:48:10 CEST 2025
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