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1000 Titel
  • Therapeutical interference with the epigenetic landscape of germ cell tumors: a comparative drug study and new mechanistical insights
1000 Autor/in
  1. Müller, Melanie R. |
  2. Burmeister, Aaron |
  3. Skowron, Margaretha A. |
  4. Stephan, Alexa |
  5. Bremmer, Felix |
  6. Wakileh, Gamal A. |
  7. Petzsch, Patrick |
  8. Köhrer, Karl |
  9. Albers, Peter |
  10. Nettersheim, Daniel |
1000 Verlag
  • BioMed Central
1000 Erscheinungsjahr 2022
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2022-01-07
1000 Erschienen in
1000 Quellenangabe
  • 14(1):5
1000 Copyrightjahr
  • 2022
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13148-021-01223-1 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742467/ |
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>Type II germ cell tumors (GCT) are the most common solid cancers in males of age 15 to 35 years. Treatment of these tumors includes cisplatin-based therapy achieving high cure rates, but also leading to late toxicities. As mainly young men are suffering from GCTs, late toxicities play a major role regarding life expectancy, and the development of therapy resistance emphasizes the need for alternative therapeutic options. GCTs are highly susceptible to interference with the epigenetic landscape; therefore, this study focuses on screening of drugs against epigenetic factors as a treatment option for GCTs. </jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>We present seven different epigenetic inhibitors efficiently decreasing cell viability in GCT cell lines including cisplatin-resistant subclones at low concentrations by targeting epigenetic modifiers and interactors, like histone deacetylases (Quisinostat), histone demethylases (JIB-04), histone methyltransferases (Chaetocin), epigenetic readers (MZ-1, LP99) and polycomb-repressive complexes (PRT4165, GSK343). Mass spectrometry-based analyses of the histone modification landscape revealed effects beyond the expected mode-of-action of each drug, suggesting a wider spectrum of activity than initially assumed. Moreover, we characterized the effects of each drug on the transcriptome of GCT cells by RNA sequencing and found common deregulations in gene expression of ion transporters and DNA-binding factors. A kinase array revealed deregulations of signaling pathways, like cAMP, JAK-STAT and WNT.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusion</jats:title> <jats:p>Our study identified seven drugs against epigenetic modifiers to treat cisplatin-resistant GCTs. Further, we extensively analyzed off-target effects and modes-of-action, which are important for risk assessment of the individual drugs.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Epigenetic modifier
lokal Histone methyltransferase inhibitor
lokal Histone demethylase inhibitor
lokal Therapy
lokal Neoplasms, Germ Cell and Embryonal/drug therapy [MeSH]
lokal Cisplatin/therapeutic use [MeSH]
lokal Male [MeSH]
lokal Germ cell tumor
lokal PROTAC
lokal Epi-drugs
lokal Adolescent [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Cell Survival/drug effects [MeSH]
lokal Cell Line/drug effects [MeSH]
lokal Cisplatin/toxicity [MeSH]
lokal Histone deacetylase inhibitor
lokal Molecular Targeted Therapy [MeSH]
lokal Antineoplastic Agents/toxicity [MeSH]
lokal Epigenetics
lokal Research
lokal Young Adult [MeSH]
lokal Antineoplastic Agents/therapeutic use [MeSH]
lokal Testicular Neoplasms/drug therapy [MeSH]
lokal Epigenesis, Genetic/drug effects [MeSH]
lokal Histone modification
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/TcO8bGxlciwgTWVsYW5pZSBSLg==|https://frl.publisso.de/adhoc/uri/QnVybWVpc3RlciwgQWFyb24=|https://frl.publisso.de/adhoc/uri/U2tvd3JvbiwgTWFyZ2FyZXRoYSBBLg==|https://frl.publisso.de/adhoc/uri/U3RlcGhhbiwgQWxleGE=|https://frl.publisso.de/adhoc/uri/QnJlbW1lciwgRmVsaXg=|https://frl.publisso.de/adhoc/uri/V2FraWxlaCwgR2FtYWwgQS4=|https://frl.publisso.de/adhoc/uri/UGV0enNjaCwgUGF0cmljaw==|https://frl.publisso.de/adhoc/uri/S8O2aHJlciwgS2FybA==|https://frl.publisso.de/adhoc/uri/QWxiZXJzLCBQZXRlcg==|https://orcid.org/0000-0002-4483-845X
1000 Hinweis
  • DeepGreen-ID: 5d0b32ad97d946bbaeff5787b4cd0337 ; 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)
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1000 Erstellt am 2024-10-02T12:06:30.678+0200
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1000 Zuletzt bearbeitet 2024-10-02T14:32:12.516+0200
1000 Objekt bearb. Wed Oct 02 14:32:12 CEST 2024
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  1. oai:frl.publisso.de:frl:6484369 |
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