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Identification of a novel quinoline-based DNA demethylating compound highly potent in cancer cells

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dc.contributor.authorZwergel, Clemens-
dc.contributor.authorSchnekenburger, Michael-
dc.contributor.authorSarno, Federica-
dc.contributor.authorBattistelli, Cecilia-
dc.contributor.authorManara, Maria C-
dc.contributor.authorStazi, Giulia-
dc.contributor.authorMazzone, Roberta-
dc.contributor.authorFioravanti, Rossella-
dc.contributor.authorGros, Christina-
dc.contributor.authorAusseil, Frédéric-
dc.contributor.authorFlorean, Cristina-
dc.contributor.authorNebbioso, Angela-
dc.contributor.authorStrippoli, Raffaele-
dc.contributor.authorUshijima, Toshikazu-
dc.contributor.authorScotlandi, Katia-
dc.contributor.authorTripodi, Marco-
dc.contributor.authorArimondo, Paola B-
dc.contributor.authorAltucci, Lucia-
dc.contributor.authorDiederich, Marc-
dc.contributor.authorMai, Antonello-
dc.contributor.authorValente, Sergio-
dc.date.accessioned2019-06-12T08:16:31Z-
dc.date.available2019-06-12T17:17:48Z-
dc.date.issued2019-05-06-
dc.identifier.citationClinical Epigenetics. 11(1):68ko_KR
dc.identifier.issn1868-7083-
dc.identifier.urihttp://hdl.handle.net/10371/153911-
dc.description.abstractBackground
DNA methyltransferases (DNMTs) are epigenetic enzymes involved in embryonic development, cell differentiation, epithelial to mesenchymal transition, and control of gene expression, whose overexpression or enhanced catalytic activity has been widely reported in cancer initiation and progression. To date, two DNMT inhibitors (DNMTi), 5-azacytidine (5-AZA) and 5-aza-2′-deoxycytidine (DAC), are approved for the treatment of myelodysplastic syndromes and acute myeloid leukemia. Nevertheless, they are chemically instable and quite toxic for healthy cells; thus, the discovery of novel DNMTi is urgent.

Results
Here, we report the identification of a new quinoline-based molecule, MC3353, as a non-nucleoside inhibitor and downregulator of DNMT. This compound was able, in promoter demethylating assays, to induce enhanced green fluorescence protein (EGFP) gene expression in HCT116 cells and transcription in a cytomegalovirus (CMV) promoter-driven luciferase reporter system in KG-1 cells. Moreover, MC3353 displayed a strong antiproliferative activity when tested on HCT116 colon cancer cells after 48 h of treatment at 0.5 μM. At higher doses, this compound provided a cytotoxic effect in double DNMT knockout HCT116 cells. MC3353 was also screened on a different panel of cancer cells (KG-1 and U-937 acute myeloid leukemia, RAJI Burkitt’s lymphoma, PC-3 prostate cancer, and MDA-MB-231 breast cancer), where it arrested cell proliferation and reduced viability after 48 h of treatment with IC50 values ranging from 0.3 to 0.9 μM. Compared to healthy cell models, MC3353 induced apoptosis (e.g., U-937 and KG-1 cells) or necrosis (e.g., RAJI cells) at lower concentrations. Importantly, together with the main DNMT3A enzyme inhibition, MC3353 was also able to downregulate the DNMT3A protein level in selected HCT116 and PC-3 cell lines. Additionally, this compound provided impairment of the epithelial-to-mesenchymal transition (EMT) by inducing E-cadherin while reducing matrix metalloproteinase (MMP2) mRNA and protein levels in PC-3 and HCT116 cells. Last, tested on a panel of primary osteosarcoma cell lines, MC3353 markedly inhibited cell growth with low single-digit micromolar IC50 ranging from 1.1 to 2.4 μM. Interestingly, in Saos-2 osteosarcoma cells, MC3353 induced both expression of genes and mineralized the matrix as evidence of osteosarcoma to osteoblast differentiation.

Conclusions
The present work describes MC3353 as a novel DNMTi displaying a stronger in cell demethylating ability than both 5-AZA and DAC, providing re-activation of the silenced ubiquitin C-terminal hydrolase L1 (UCHL1) gene. MC3353 displayed dose- and time-dependent antiproliferative activity in several cancer cell types, inducing cell death and affecting EMT through E-cadherin and MMP2 modulation. In addition, this compound proved efficacy even in primary osteosarcoma cell models, through the modulation of genes involved in osteoblast differentiation.
ko_KR
dc.description.sponsorshipThis work was supported by COST Action CM1406 (PBA, LA, AM, SV); by Ricerca Finalizzata 2013 PE-2013-02355271 (AM); by PRIN 2016 (prot. 20152TE5PK) (AM, LA); by AIRC grants n. 19162 (AM), 17217 (LA), and 18843 (MT); by NIH funds n. R01GM114306 (AM) and BLUEPRINT n. 282510 (AM, LA); by Programma VALERE: Vanvitelli per la Ricerca (LA) and the Italian-Flag Project-EPIGEN (LA); and by Pasteur Institute-Cenci Bolognetti Foundation (MT). MS was supported by a “Waxweiler grant for cancer prevention
research” from the Action Lions “Vaincre le Cancer.” CF is a recipient of a Télévie Luxembourg fellowship. The work at LBMCC was supported by the “Recherche Cancer et Sang” foundation, by the “Recherches Scientifiques Luxembourg” association, by the “Een Häerz fir kriibskrank Kanner” association, by the Action LIONS “Vaincre le Cancer” association, and by Télévie Luxembourg. MD was supported by the Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Korea; the Tumor Microenvironment GCRC (2011-0030001) from the National Research Foundation funded by the Ministry of Science and ICT of Korea; the Creative-Pioneering Researchers Program through Seoul National University (SNU) [Funding number: 370C-20160062]; and Brain Korea (BK) 21 Plus program, Korea.
ko_KR
dc.language.isoenko_KR
dc.publisherBioMed Centralko_KR
dc.subjectEpigeneticsko_KR
dc.subjectCancerko_KR
dc.subjectDNMT inhibitorko_KR
dc.subjectQuinoline-based compoundko_KR
dc.subjectGene expressionko_KR
dc.titleIdentification of a novel quinoline-based DNA demethylating compound highly potent in cancer cellsko_KR
dc.typeArticleko_KR
dc.identifier.doi10.1186/s13148-019-0663-8-
dc.language.rfc3066en-
dc.rights.holderThe Author(s).-
dc.date.updated2019-05-12T20:36:01Z-
Appears in Collections:
College of Pharmacy (약학대학)Dept. of Pharmacy (약학과)Journal Papers (저널논문_약학과)
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