Literature DB >> 16886598

Antiproliferative and proapoptotic activities of pyranoxanthenones, pyranothioxanthenones and their pyrazole-fused derivatives in HL-60 cells.

Elisabeth M Perchellet1, Mary M Ward, Alexios-Leandros Skaltsounis, Ioannis K Kostakis, Nicole Pouli, Panagiotis Marakos, Jean-Pierre H Perchellet.   

Abstract

BACKGROUND: Synthetic pyranoxanthenones, pyranothioxanthenones and their pyrazole-fused derivatives, which bind to DNA, block the G2 + M-phases of the cell cycle and inhibit the proliferation of ascitic and solid tumor cell lines in vitro, were tested for their ability to induce apoptosis in the HL-60 cell system.
MATERIALS AND METHODS: Various markers of tumor cell metabolism, apoptosis induction and mitochondrial permeability transition (MPT) were assayed in vitro to evaluate drug cytotoxicity.
RESULTS: All these compounds, and especially the pyrazole-fused pyranoxanthenones 7, 8 and 10, which were effective in the 3-5 microM range and were more potent than the pyranoxanthenones, reduced the proliferation of HL-60 cells at 2 and 4 days. These antitumor drugs inhibited DNA synthesis at 2 h in relation to their ability to block the cellular uptake of purine and pyrimidine nucleosides within 15 min. Internmucleosomal DNA fragmentation, a late marker of apoptosis, was induced in a concentration-dependent manner by 7 and 10 at 24 h. Poly(ADP-ribose) polymerase-1 (PARP-1) cleavage, an early event required for cells committed to apoptosis, was detected within 12 h in HL-60 cells treated with 7 and 10. In accord with the fact that the caspase cascade is responsible for PARP-1 cleavage, 7 and 10 induced the activities of initiator caspases-2 and -9 and effector caspase-3 within 9 h in HL-60 cells. The release of mitochondrial cytochrome c (Cyt c) was also detected within 9 h in HL-60 cells treated with 7 and 10, consistent with the fact that Cyt c is the apoptotic trigger that activates caspase-9. However, 7 and 10 neither caused the rapid collapse of mitochondrial transmembrane potential, nor the mitochondrial swelling linked to MPT.
CONCLUSION: Pyrazole-fused pyranoxanthenones are DNA-interacting antiproliferative drugs that do not directly target mitochondria in cell and cell-free systems to induce the intrinsic pathway of apoptosis.

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Year:  2006        PMID: 16886598

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  3 in total

1.  Antitumor effects of synthetic 6,7-annulated-4-substituted indole compounds in L1210 leukemic cells in vitro.

Authors:  Jean-Pierre H Perchellet; Andrew M Waters; Elisabeth M Perchellet; Paul D Thornton; Neil Brown; David Hill; Ben Neuenswander; Gerald H Lushington; Conrad Santini; Nalin Chandrasoma; Keith R Buszek
Journal:  Anticancer Res       Date:  2012-11       Impact factor: 2.480

2.  Crystal structure of 6-amino-4-(3-bromo-4-meth-oxy-phen-yl)-3-methyl-2,4-di-hydro-pyrano[2,3-c]pyrazole-5-carbo-nitrile dimethyl sulfoxide monosolvate.

Authors:  Sammer Yousuf; Huma Bano; Munira Taj Muhammad; Khalid Mohammed Khan
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2015-06-06

3.  Biological Validation of Novel Polysubstituted Pyrazole Candidates with in Vitro Anticancer Activities.

Authors:  Hoda H Fahmy; Nagy M Khalifa; Magda M F Ismail; Hend M El-Sahrawy; Eman S Nossier
Journal:  Molecules       Date:  2016-02-26       Impact factor: 4.411

  3 in total

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