Anticancer Effects of the Novel Pyrazolyl-Urea GeGe-3

Author:

Williams Ashleigh1,Cooper Emma1,Clark Bethany1,Perry Laura1,Ponassi Marco2,Iervasi Erika2ORCID,Brullo Chiara3ORCID,Greenhough Alexander1,Ladomery Michael1

Affiliation:

1. Centre for Research in Biosciences, School of Applied Sciences, University of the West of England, Coldharbour Lane, Frenchay, Bristol BS16 1QY, UK

2. Proteomics and Mass Spectrometry Unit, IRCCS Ospedale Policlinico San Martino, L.go. R. Benzi 10, 16132 Genova, Italy

3. Department of Pharmacy, Medicinal Chemistry Section, University of Genova, Viale Benedetto XV, 3, 16132 Genova, Italy

Abstract

In a screen of over 200 novel pyrazole compounds, ethyl 1-(2-hydroxypentyl)-5-(3-(3-(trifluoromethyl) phenyl)ureido)-1H-pyrazole-4-carboxylate (named GeGe-3) has emerged as a potential anticancer compound. GeGe-3 displays potent anti-angiogenic properties through the presumptive targeting of the protein kinase DMPK1 and the Ca2+-binding protein calreticulin. We further explored the anticancer potential of GeGe-3 on a range of established cancer cell lines, including PC3 (prostate adenocarcinoma), SKMEL-28 (cutaneous melanoma), SKOV-3 (ovarian adenocarcinoma), Hep-G2 (hepatocellular carcinoma), MDA-MB231, SKBR3, MCF7 (breast adenocarcinoma), A549 (lung carcinoma), and HeLa (cervix epithelioid carcinoma). At concentrations in the range of 10 μM, GeGe-3 significantly restricted cell proliferation and metabolism. GeGe-3 also reduced PC3 cell migration in a standard wound closure and trans-well assay. Together, these results confirm the anticancer potential of GeGe-3 and underline the need for more detailed pre-clinical investigations into its molecular targets and mechanisms of action.

Funder

Wellcome Trust

Bowel Cancer UK

Sosei Heptares

Italian Ministry of Health

Publisher

MDPI AG

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