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1000 Titel
  • Drug repurposing using transcriptome sequencing and virtual drug screening in a patient with glioblastoma
1000 Autor/in
  1. Saeed, Mohamed E. M. |
  2. Kadioglu, Onat |
  3. Greten, Henry Johannes |
  4. Yildirim, Adem |
  5. Mayr, Katharina |
  6. Wenz, Frederik |
  7. Giordano, Frank A. |
  8. Efferth, Thomas |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-12-12
1000 Erschienen in
1000 Quellenangabe
  • 39(3):670-685
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s10637-020-01037-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8068653/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background Precision medicine and drug repurposing are attractive strategies, especially for tumors with worse prognosis. Glioblastoma is a highly malignant brain tumor with limited treatment options and short survival times. We identified novel BRAF (47-438del) and PIK3R1 (G376R) mutations in a glioblastoma patient by RNA-sequencing. Methods The protein expression of BRAF and PIK3R1 as well as the lack of EGFR expression as analyzed by immunohistochemistry corroborated RNA-sequencing data. The expression of additional markers (AKT, SRC, mTOR, NF-κB, Ki-67) emphasized the aggressiveness of the tumor. Then, we screened a chemical library of > 1500 FDA-approved drugs and > 25,000 novel compounds in the ZINC database to find established drugs targeting BRAF47-438del and PIK3R1-G376R mutated proteins. Results Several compounds (including anthracyclines) bound with higher affinities than the control drugs (sorafenib and vemurafenib for BRAF and PI-103 and LY-294,002 for PIK3R1). Subsequent cytotoxicity analyses showed that anthracyclines might be suitable drug candidates. Aclarubicin revealed higher cytotoxicity than both sorafenib and vemurafenib, whereas idarubicin and daunorubicin revealed higher cytotoxicity than LY-294,002. Liposomal formulations of anthracyclines may be suitable to cross the blood brain barrier. Conclusions In conclusion, we identified novel small molecules via a drug repurposing approach that could be effectively used for personalized glioblastoma therapy especially for patients carrying BRAF47-438del and PIK3R1-G376R mutations.
1000 Sacherschließung
lokal Cell Line, Tumor [MeSH]
lokal Aged [MeSH]
lokal Proto-Oncogene Proteins B-raf/genetics [MeSH]
lokal Anthracyclines/pharmacology [MeSH]
lokal Antineoplastic Agents/pharmacology [MeSH]
lokal Glioblastoma/metabolism [MeSH]
lokal Targeted chemotherapy
lokal Proto-Oncogene Proteins B-raf/metabolism [MeSH]
lokal Glioblastoma/drug therapy [MeSH]
lokal Preclinical Studies
lokal Class Ia Phosphatidylinositol 3-Kinase/metabolism [MeSH]
lokal Glioblastoma/genetics [MeSH]
lokal Temozolomide/pharmacology [MeSH]
lokal Mutation [MeSH]
lokal Brain Neoplasms/genetics [MeSH]
lokal Drug repurposing
lokal Class Ia Phosphatidylinositol 3-Kinase/genetics [MeSH]
lokal Humans [MeSH]
lokal Anthracyclines/therapeutic use [MeSH]
lokal Precision medicine
lokal Drug Repositioning [MeSH]
lokal Antineoplastic Agents/therapeutic use [MeSH]
lokal Temozolomide/therapeutic use [MeSH]
lokal Transcriptome [MeSH]
lokal Genotype [MeSH]
lokal Brain Neoplasms/drug therapy [MeSH]
lokal Virtual drug screening
lokal Brain Neoplasms/metabolism [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/U2FlZWQsIE1vaGFtZWQgRS4gTS4=|https://frl.publisso.de/adhoc/uri/S2FkaW9nbHUsIE9uYXQ=|https://frl.publisso.de/adhoc/uri/R3JldGVuLCBIZW5yeSBKb2hhbm5lcw==|https://frl.publisso.de/adhoc/uri/WWlsZGlyaW0sIEFkZW0=|https://frl.publisso.de/adhoc/uri/TWF5ciwgS2F0aGFyaW5h|https://frl.publisso.de/adhoc/uri/V2VueiwgRnJlZGVyaWs=|https://frl.publisso.de/adhoc/uri/R2lvcmRhbm8sIEZyYW5rIEEu|https://orcid.org/0000-0002-2637-1681
1000 Hinweis
  • DeepGreen-ID: 8d1741180cc74fe89d03a0e6b3091c30 ; 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 2023-11-17T16:07:35.584+0100
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1000 Zuletzt bearbeitet Fri Dec 01 07:50:10 CET 2023
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