Cyclin-dependent kinase inhibitors exert distinct effects on patient-derived 2D and 3D glioblastoma cell culture models.


Journal

Cell death discovery
ISSN: 2058-7716
Titre abrégé: Cell Death Discov
Pays: United States
ID NLM: 101665035

Informations de publication

Date de publication:
15 Mar 2021
Historique:
received: 29 09 2020
accepted: 23 12 2020
revised: 23 11 2020
entrez: 16 3 2021
pubmed: 17 3 2021
medline: 17 3 2021
Statut: epublish

Résumé

Current therapeutic approaches have met limited clinical success for glioblastoma multiforme (GBM). Since GBM harbors genomic alterations in cyclin-dependent kinases (CDKs), targeting these structures with specific inhibitors (CDKis) is promising. Here, we describe the antitumoral potential of selective CDKi on low-passage GBM 2D- and 3D models, cultured as neurospheres (NSCs) or glioma stem-like cells (GSCs). By applying selective CDK4/6i abemaciclib and palbociclib, and the more global CDK1/2/5/9-i dinaciclib, different effects were seen. Abemaciclib and dinaciclib significantly affected viability in 2D- and 3D models with clearly visible changes in morphology. Palbociclib had weaker and cell line-specific effects. Motility and invasion were highly affected. Abemaciclib and dinaciclib additionally induced senescence. Also, mitochondrial dysfunction and generation of mitochondrial reactive oxygen species (ROS) were seen. While autophagy was predominantly visible after abemaciclib treatment, dinaciclib evoked γ-H2AX-positive double-strand breaks that were boosted by radiation. Notably, dual administration of dinaciclib and abemaciclib yielded synergistic effects in most cases, but the simultaneous combination with standard chemotherapeutic agent temozolomide (TMZ) was antagonistic. RNA-based microarray analysis showed that gene expression was significantly altered by dinaciclib: genes involved in cell-cycle regulation (different CDKs and their cyclins, SMC3), mitosis (PLK1, TTK), transcription regulation (IRX3, MEN1), cell migration/division (BCAR1), and E3 ubiquitination ligases (RBBP6, FBXO32) were downregulated, whereas upregulation was seen in genes mediating chemotaxis (CXCL8, IL6, CCL2), and DNA-damage or stress (EGR1, ARC, GADD45A/B). In a long-term experiment, resistance development was seen in 1/5 cases treated with dinaciclib, but this could be prevented by abemaciclib. Vice versa, adding TMZ abrogated therapeutic effects of dinaciclib and growth was comparable to controls. With this comprehensive analysis, we confirm the therapeutic activity of selective CDKi in GBM. In addition to the careful selection of individual drugs, the timing of each combination partner needs to be considered to prevent resistance.

Identifiants

pubmed: 33723248
doi: 10.1038/s41420-021-00423-1
pii: 10.1038/s41420-021-00423-1
pmc: PMC7961149
doi:

Types de publication

Journal Article

Langues

eng

Pagination

54

Références

Cell Mol Life Sci. 2013 Feb;70(4):661-87
pubmed: 22864622
Cancer Med. 2019 Aug;8(9):4348-4358
pubmed: 31207099
Biochim Biophys Acta. 2010 Jun-Jul;1797(6-7):1171-7
pubmed: 20153717
Nucleic Acids Res. 2017 Oct 13;45(18):10564-10582
pubmed: 28985345
Anal Biochem. 2018 Jul 1;552:50-59
pubmed: 28711444
Cell Oncol (Dordr). 2018 Dec;41(6):663-675
pubmed: 30178167
Transl Oncol. 2015 Aug;8(4):295-307
pubmed: 26310376
Cells. 2019 Jan 03;8(1):
pubmed: 30609792
J Exp Clin Cancer Res. 2018 Sep 20;37(1):233
pubmed: 30236142
PLoS One. 2013 Aug 07;8(8):e71070
pubmed: 23951083
Signal Transduct Target Ther. 2018 Apr 13;3:9
pubmed: 29666673
EBioMedicine. 2019 Jan;39:182-193
pubmed: 30579871
Cells. 2019 Apr 06;8(4):
pubmed: 30959874
Cancer Discov. 2016 Apr;6(4):353-67
pubmed: 26658964
Drug Metab Dispos. 2015 Sep;43(9):1360-71
pubmed: 26149830
Cell Death Dis. 2019 Jan 25;10(2):73
pubmed: 30683840
Cancer Res. 2008 Nov 1;68(21):8657-60
pubmed: 18974105
Pharm Res. 2010 Oct;27(10):2162-74
pubmed: 20668920
Biochim Biophys Acta. 2003 Sep 30;1606(1-3):137-46
pubmed: 14507434
Cancer Sci. 2020 Feb;111(2):749-759
pubmed: 31849147
Proc Natl Acad Sci U S A. 2019 Nov 19;116(47):23714-23723
pubmed: 31712430
J Pharmacol Exp Ther. 2016 Feb;356(2):354-65
pubmed: 26585571
Br J Cancer. 2017 Mar 28;116(7):912-922
pubmed: 28222068
Mol Med Rep. 2017 Dec;16(6):9715-9720
pubmed: 29039550
Oncotarget. 2017 Oct 10;8(53):90662-90673
pubmed: 29207595
Oncol Lett. 2014 May;7(5):1673-1678
pubmed: 24765199
J Signal Transduct. 2012;2012:646354
pubmed: 21977319
Semin Cancer Biol. 2020 Feb;60:262-273
pubmed: 31654711
IUBMB Life. 2007 Jul;59(7):419-26
pubmed: 17654117
Chem Biol Interact. 2017 Dec 25;278:179-188
pubmed: 28989041
Cancer Sci. 2020 Jun;111(6):2132-2145
pubmed: 32304130
Sci Rep. 2020 Mar 13;10(1):4714
pubmed: 32170212
Oncogene. 2017 Sep 14;36(37):5321-5330
pubmed: 28534518
Cell Cycle. 2017 Aug 3;16(15):1453-1464
pubmed: 28678584
Oncotarget. 2015 Dec 8;6(39):41794-808
pubmed: 26540629
Free Radic Biol Med. 2016 Nov;100:14-31
pubmed: 27085844
Mol Cancer Ther. 2010 Aug;9(8):2344-53
pubmed: 20663931
Mol Cancer. 2011 Jun 06;10:69
pubmed: 21639944
Cell Rep. 2018 Mar 13;22(11):2978-2994
pubmed: 29539425
Am J Transl Res. 2017 May 15;9(5):2163-2180
pubmed: 28559969
Adv Exp Med Biol. 2013;793:1-19
pubmed: 24104470
Cancer Biol Ther. 2011 Oct 1;12(7):598-609
pubmed: 21768779
Am J Pathol. 2014 Jun;184(6):1630-42
pubmed: 24726643
Mol Cancer Ther. 2020 Jan;19(1):3-12
pubmed: 31909732
Oncotarget. 2014 Jun 30;5(12):4467-79
pubmed: 24962950
Cells. 2019 Aug 09;8(8):
pubmed: 31405017
Gut. 2018 Dec;67(12):2142-2155
pubmed: 29080858
Biochem Pharmacol. 2017 Jan 15;124:29-42
pubmed: 27816545
Int J Cancer. 2018 May 15;142(10):2139-2152
pubmed: 29243224
Mol Cancer Ther. 2015 Sep;14(9):2090-102
pubmed: 26141949
Oncogene. 2007 Jul 19;26(33):4825-32
pubmed: 17297447
Sci Data. 2018 Jul 24;5:180145
pubmed: 30040082
Oncotarget. 2017 May 10;8(41):69493-69507
pubmed: 29050219
Cancer Lett. 2019 Sep 10;459:216-226
pubmed: 31199987
Bioorg Med Chem Lett. 2019 Oct 15;29(20):126637
pubmed: 31477350
Sci Rep. 2017 Mar 31;7:45577
pubmed: 28361959
Cell Rep. 2016 Nov 22;17(9):2367-2381
pubmed: 27880910

Auteurs

Christin Riess (C)

University Children's Hospital, Rostock University Medical Centre, Ernst-Heydemann-Straße 8, 18057, Rostock, Germany.
Department of Medicine Clinic III - Hematology, Oncology, Palliative Medicine, Rostock University Medical Center, Rostock University Medical Centre, Ernst-Heydemann-Str. 6, 18057, Rostock, Germany.

Dirk Koczan (D)

Core Facility for Microarray Analysis, Institute for Immunology, Rostock University Medical Centre, 18057, Rostock, Germany.

Björn Schneider (B)

Institute of Pathology, Strempelstraße 14, 18055 Rostock, Rostock University Medical Centre, 18057, Rostock, Germany.

Charlotte Linke (C)

University Children's Hospital, Rostock University Medical Centre, Ernst-Heydemann-Straße 8, 18057, Rostock, Germany.

Katharina Del Moral (K)

University Children's Hospital, Rostock University Medical Centre, Ernst-Heydemann-Straße 8, 18057, Rostock, Germany.

Carl Friedrich Classen (CF)

University Children's Hospital, Rostock University Medical Centre, Ernst-Heydemann-Straße 8, 18057, Rostock, Germany.

Claudia Maletzki (C)

Department of Medicine Clinic III - Hematology, Oncology, Palliative Medicine, Rostock University Medical Center, Rostock University Medical Centre, Ernst-Heydemann-Str. 6, 18057, Rostock, Germany. claudia.maletzki@med.uni-rostock.de.

Classifications MeSH