| Literature DB >> 30900116 |
Ludovica Taglieri1, Francesco Saccoliti2, Alice Nicolai1,3, Giovanna Peruzzi4, Valentina Noemi Madia2, Valeria Tudino2, Antonella Messore2, Roberto Di Santo2, Marco Artico3, Samanta Taurone3, Maurizio Salvati5, Roberta Costi6, Susanna Scarpa1.
Abstract
Recently, some synthetic nitrogen-based heterocyclic molecules, such as PJ34, have shown pronounced antitumor activity. Therefore, we designed and synthesized new derivatives characterized by a nitrogen-containing scaffold and evaluated their antiproliferative properties in tumor cells. We herein report the effects of three newly synthesized compounds on cell lines from three different human cancers: triple-negative breast cancer, colon carcinoma and glioblastoma. We found that two of these compounds did not affect proliferation, while the third significantly inhibited replication of the three cell lines. Moreover, this third molecule at 20 μM led to the upregulation of p21 and p27 and blockage of the cell cycle at G0/G1; in addition, it induced apoptosis in all three cell lines when used at higher concentrations (30-50 μM). The results demonstrate that this compound is a potent inhibitor of replication, an inducer of apoptosis and a negative regulator of cell cycle progression for cancer cells of different histotypes. Our data suggest a potential role for this new molecule as an interesting and powerful tool for new approaches in treating various cancers.Entities:
Keywords: Breast cancer; Colon carcinoma; Glioblastoma multiforme; PJ34; Phenathridinone; Pyrimidine
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Year: 2019 PMID: 30900116 DOI: 10.1007/s10637-019-00762-y
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850