Targeting the CALCB/RAMP1 axis inhibits growth of Ewing sarcoma.
Animals
Calcitonin Gene-Related Peptide
/ antagonists & inhibitors
Cell Line, Tumor
Cell Proliferation
/ drug effects
Gene Expression Regulation, Neoplastic
Humans
Mice
Mice, Inbred NOD
Microsatellite Repeats
/ genetics
RNA Interference
RNA, Small Interfering
/ metabolism
Receptor Activity-Modifying Protein 1
/ antagonists & inhibitors
Sarcoma, Ewing
/ drug therapy
Small Molecule Libraries
/ pharmacology
Transplantation, Heterologous
Journal
Cell death & disease
ISSN: 2041-4889
Titre abrégé: Cell Death Dis
Pays: England
ID NLM: 101524092
Informations de publication
Date de publication:
11 02 2019
11 02 2019
Historique:
received:
09
12
2018
accepted:
17
01
2019
revised:
16
01
2019
entrez:
12
2
2019
pubmed:
12
2
2019
medline:
13
2
2020
Statut:
epublish
Résumé
Ewing sarcoma (EwS) is an aggressive cancer characterized by chromosomal translocations generating fusions of the EWSR1 gene with ETS transcription factors (in 85% FLI1). EWSR1-FLI1 induces gene expression via binding to enhancer-like GGAA-microsatellites, whose activity correlates with the number of consecutive GGAA-repeats. Herein we investigate the role of the secretory neuropeptide CALCB (calcitonin-related polypeptide β) in EwS, which signals via the CGRP (calcitonin gene-related peptide) receptor complex, containing RAMP1 (receptor activity modifying protein 1) as crucial part for receptor specificity. Analysis of 2678 gene expression microarrays comprising 50 tumor entities and 71 normal tissue types revealed that CALCB is specifically and highly overexpressed in EwS. Time-course knockdown experiments showed that CALCB expression is tightly linked to that of EWSR1-FLI1. Consistently, gene set enrichment analyses of genes whose expression in primary EwS is correlated to that of CALCB indicated that it is co-expressed with other EWSR1-FLI1 target genes and associated with signatures involved in stemness and proliferation. Chromatin immunoprecipitation followed by sequencing (ChIP-seq) data for FLI1 and histone marks from EwS cell lines demonstrated that EWSR1-FLI1 binds to a GGAA-microsatellite close to CALCB, which exhibits characteristics of an active enhancer. Reporter assays confirmed the strong EWSR1-FLI1- and length-dependent enhancer activity of this GGAA-microsatellite. Mass spectrometric analyses of EwS cell culture supernatants demonstrated that CALCB is secreted by EwS cells. While short-term RNA interference-mediated CALCB knockdown had no effect on proliferation and clonogenic growth of EwS cells in vitro, its long-term knockdown decreased EwS growth in vitro and in vivo. Similarly, knockdown of RAMP1 reduced clonogenic/spheroidal growth and tumorigenicity, and small-molecule inhibitors directed against the RAMP1-comprising CGRP receptor reduced growth of EwS. Collectively, our findings suggest that CALCB is a direct EWSR1-FLI1 target and that targeting the CALCB/RAMP1 axis may offer a new therapeutic strategy for inhibition of EwS growth.
Identifiants
pubmed: 30741933
doi: 10.1038/s41419-019-1372-0
pii: 10.1038/s41419-019-1372-0
pmc: PMC6370763
doi:
Substances chimiques
CALCB protein, human
0
RAMP1 protein, human
0
RNA, Small Interfering
0
Receptor Activity-Modifying Protein 1
0
Small Molecule Libraries
0
Calcitonin Gene-Related Peptide
JHB2QIZ69Z
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
116Références
J Clin Oncol. 2010 Jul 10;28(20):3284-91
pubmed: 20547982
Nature. 1998 May 28;393(6683):333-9
pubmed: 9620797
Proc Natl Acad Sci U S A. 2008 Jul 22;105(29):10149-54
pubmed: 18626011
J Hypertens Suppl. 1986 Dec;4(5):S102-5
pubmed: 3553470
Endocr Rev. 1996 Oct;17(5):533-85
pubmed: 8897024
Molecules. 2018 Jun 19;23(6):
pubmed: 29921764
J Mol Endocrinol. 1989 Nov;3(3):247-52
pubmed: 2590386
PLoS One. 2011 Apr 29;6(4):e19305
pubmed: 21559395
Proc Natl Acad Sci U S A. 2005 Oct 25;102(43):15545-50
pubmed: 16199517
Mol Cancer Res. 2012 Jan;10(1):52-65
pubmed: 22080479
Nat Commun. 2018 Aug 9;9(1):3184
pubmed: 30093639
Oncotarget. 2017 May 23;8(21):34141-34163
pubmed: 27191748
Nat Rev Neurol. 2018 Jun;14(6):338-350
pubmed: 29691490
Genomics. 1993 Mar;15(3):525-9
pubmed: 8468047
Cancer Res. 2005 Jun 1;65(11):4633-44
pubmed: 15930281
Cancer Cell. 2014 Nov 10;26(5):668-681
pubmed: 25453903
Biostatistics. 2003 Apr;4(2):249-64
pubmed: 12925520
Cancer Cell. 2007 May;11(5):421-9
pubmed: 17482132
Nucleic Acids Res. 2005 Nov 10;33(20):e175
pubmed: 16284200
Nat Genet. 2015 Sep;47(9):1073-8
pubmed: 26214589
Nature. 1992 Sep 10;359(6391):162-5
pubmed: 1522903
Oncoimmunology. 2018 Jul 23;7(9):e1481558
pubmed: 30228952
Science. 2018 Aug 31;361(6405):
pubmed: 30166462
FEBS Lett. 1989 Oct 9;256(1-2):170-4
pubmed: 2553478
Clin Exp Pharmacol Physiol. 2007 Oct;34(10):963-71
pubmed: 17714080
J Clin Endocrinol Metab. 1987 Apr;64(4):809-17
pubmed: 3493259
Nature. 2012 Sep 6;489(7414):57-74
pubmed: 22955616
Clin Cancer Res. 2007 Apr 15;13(8):2429-40
pubmed: 17438102
Nat Rev Dis Primers. 2018 Jul 5;4(1):5
pubmed: 29977059
FEBS Lett. 1986 Dec 1;209(1):97-103
pubmed: 3492393
Cell Cycle. 2009 Feb 1;8(3):498-504
pubmed: 19177017
Methods. 2001 Dec;25(4):402-8
pubmed: 11846609
Oncogene. 2016 Jun 16;35(24):3092-102
pubmed: 26455317
Clin Cancer Res. 2000 Jan;6(1):139-46
pubmed: 10656442
Cancer Discov. 2014 Nov;4(11):1326-41
pubmed: 25186949
Cancer Discov. 2014 Nov;4(11):1342-53
pubmed: 25223734
Cell Rep. 2015 Feb 24;10(7):1082-95
pubmed: 25704812
Pathologe. 1987 May;8(3):138-40
pubmed: 3303008
Oncotarget. 2017 Aug 4;9(2):1587-1601
pubmed: 29416716
FEBS Lett. 1985 Apr 22;183(2):403-7
pubmed: 2985435