Cargando…

3-Bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo

In search for new anticancer agents, we have evaluated the antiinvasive and antimigrative properties of recently developed synthetic coumarin derivatives among which two compounds revealed important activity: 3-chlorophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate and 3-bromophenyl 6-acet...

Descripción completa

Detalles Bibliográficos
Autores principales: Kempen, I, Papapostolou, D, Thierry, N, Pochet, L, Counerotte, S, Masereel, B, Foidart, J-M, Reboud-Ravaux, M, Noël, A, Pirotte, B
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376372/
https://www.ncbi.nlm.nih.gov/pubmed/12671713
http://dx.doi.org/10.1038/sj.bjc.6600856
_version_ 1782154731257331712
author Kempen, I
Papapostolou, D
Thierry, N
Pochet, L
Counerotte, S
Masereel, B
Foidart, J-M
Reboud-Ravaux, M
Noël, A
Pirotte, B
author_facet Kempen, I
Papapostolou, D
Thierry, N
Pochet, L
Counerotte, S
Masereel, B
Foidart, J-M
Reboud-Ravaux, M
Noël, A
Pirotte, B
author_sort Kempen, I
collection PubMed
description In search for new anticancer agents, we have evaluated the antiinvasive and antimigrative properties of recently developed synthetic coumarin derivatives among which two compounds revealed important activity: 3-chlorophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate and 3-bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate. Both drugs were able to inhibit cell invasion markedly in a Boyden chamber assay, the bromo derivative being more potent than the reference matrix metalloprotease (MMP) inhibitor GI 129471. In vivo, tumour growth was reduced when nude mice grafted with HT1080 or MDA-MB231 cells were treated i.p. 3 days week(−1) with the bromo coumarin derivative. These effects were not associated with the inhibition of urokinase, plasmin, MMP-2 or MMP-9. The mechanism of action of the drugs remains to be elucidated. However, these two coumarin derivatives may serve as new lead compounds of an original class of antitumour agents.
format Text
id pubmed-2376372
institution National Center for Biotechnology Information
language English
publishDate 2003
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-23763722009-09-10 3-Bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo Kempen, I Papapostolou, D Thierry, N Pochet, L Counerotte, S Masereel, B Foidart, J-M Reboud-Ravaux, M Noël, A Pirotte, B Br J Cancer Experimental Therapeutics In search for new anticancer agents, we have evaluated the antiinvasive and antimigrative properties of recently developed synthetic coumarin derivatives among which two compounds revealed important activity: 3-chlorophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate and 3-bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate. Both drugs were able to inhibit cell invasion markedly in a Boyden chamber assay, the bromo derivative being more potent than the reference matrix metalloprotease (MMP) inhibitor GI 129471. In vivo, tumour growth was reduced when nude mice grafted with HT1080 or MDA-MB231 cells were treated i.p. 3 days week(−1) with the bromo coumarin derivative. These effects were not associated with the inhibition of urokinase, plasmin, MMP-2 or MMP-9. The mechanism of action of the drugs remains to be elucidated. However, these two coumarin derivatives may serve as new lead compounds of an original class of antitumour agents. Nature Publishing Group 2003-04-07 2003-04-01 /pmc/articles/PMC2376372/ /pubmed/12671713 http://dx.doi.org/10.1038/sj.bjc.6600856 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Experimental Therapeutics
Kempen, I
Papapostolou, D
Thierry, N
Pochet, L
Counerotte, S
Masereel, B
Foidart, J-M
Reboud-Ravaux, M
Noël, A
Pirotte, B
3-Bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo
title 3-Bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo
title_full 3-Bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo
title_fullStr 3-Bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo
title_full_unstemmed 3-Bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo
title_short 3-Bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo
title_sort 3-bromophenyl 6-acetoxymethyl-2-oxo-2h-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo
topic Experimental Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376372/
https://www.ncbi.nlm.nih.gov/pubmed/12671713
http://dx.doi.org/10.1038/sj.bjc.6600856
work_keys_str_mv AT kempeni 3bromophenyl6acetoxymethyl2oxo2h1benzopyran3carboxylateinhibitscancercellinvasioninvitroandtumourgrowthinvivo
AT papapostoloud 3bromophenyl6acetoxymethyl2oxo2h1benzopyran3carboxylateinhibitscancercellinvasioninvitroandtumourgrowthinvivo
AT thierryn 3bromophenyl6acetoxymethyl2oxo2h1benzopyran3carboxylateinhibitscancercellinvasioninvitroandtumourgrowthinvivo
AT pochetl 3bromophenyl6acetoxymethyl2oxo2h1benzopyran3carboxylateinhibitscancercellinvasioninvitroandtumourgrowthinvivo
AT counerottes 3bromophenyl6acetoxymethyl2oxo2h1benzopyran3carboxylateinhibitscancercellinvasioninvitroandtumourgrowthinvivo
AT masereelb 3bromophenyl6acetoxymethyl2oxo2h1benzopyran3carboxylateinhibitscancercellinvasioninvitroandtumourgrowthinvivo
AT foidartjm 3bromophenyl6acetoxymethyl2oxo2h1benzopyran3carboxylateinhibitscancercellinvasioninvitroandtumourgrowthinvivo
AT reboudravauxm 3bromophenyl6acetoxymethyl2oxo2h1benzopyran3carboxylateinhibitscancercellinvasioninvitroandtumourgrowthinvivo
AT noela 3bromophenyl6acetoxymethyl2oxo2h1benzopyran3carboxylateinhibitscancercellinvasioninvitroandtumourgrowthinvivo
AT pirotteb 3bromophenyl6acetoxymethyl2oxo2h1benzopyran3carboxylateinhibitscancercellinvasioninvitroandtumourgrowthinvivo