Epanorin, a lichen secondary metabolite, inhibits proliferation of MCF-7 breast cancer cells

Abstract Background: Epanorin (EP) is a secondary metabolite of the Acarospora lichenic species. EP has been found in lichenic extracts with antimicrobial activity, and UV-absorption properties have been described for closely related molecules; however, its antiproliferative activity in cancer cells has not yet been explored. It has been hypothesized that EP inhibits cancer cell growth. MCF-7 breast cancer cells, normal fibroblasts, and the non-transformed HEK-293 cell line were exposed to increasing concentrations of EP, and proliferation was assessed by the sulforhodamine-B assay. Results: MCF-7 cells exposed to EP were examined for cell cycle progression using flow cytometry, and DNA fragmentation was examined using the TUNEL assay. In addition, EP's mutagenic activity was assessed using the Salmonella typhimurium reverse mutation assay. The data showed that EP inhibits proliferation of MCF-7 cells, and it induces cell cycle arrest in G0/G1 through a DNA fragmentation-independent mechanism. Furthermore, EP's lack of overt cytotoxicity in the normal cell line HEK-293 and human fibroblasts in cell culture is supported by the absence of mutagenic activity of EP. Conclusion: EP emerges as a suitable molecule for further studies as a potential antineoplastic agent.

Saved in:
Bibliographic Details
Main Authors: Palacios-Moreno,Juan, Rubio,Cecilia, Quilhot,Wanda, Cavieres,M. Fernanda, Peña,Eduardo de la, Quiñones,Natalia V., Díaz,Hugo, Carrión,Flavio, Henríquez-Roldán,Carlos F., Weinstein-Oppenheimer,Caroline R.
Format: Digital revista
Language:English
Published: Sociedad de Biología de Chile 2019
Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602019000100251
Tags: Add Tag
No Tags, Be the first to tag this record!
id oai:scielo:S0716-97602019000100251
record_format ojs
spelling oai:scielo:S0716-976020190001002512019-12-02Epanorin, a lichen secondary metabolite, inhibits proliferation of MCF-7 breast cancer cellsPalacios-Moreno,JuanRubio,CeciliaQuilhot,WandaCavieres,M. FernandaPeña,Eduardo de laQuiñones,Natalia V.Díaz,HugoCarrión,FlavioHenríquez-Roldán,Carlos F.Weinstein-Oppenheimer,Caroline R. Epanorin Cancer Cytotoxicity Mutagenesis Cell cycle Apoptosis Abstract Background: Epanorin (EP) is a secondary metabolite of the Acarospora lichenic species. EP has been found in lichenic extracts with antimicrobial activity, and UV-absorption properties have been described for closely related molecules; however, its antiproliferative activity in cancer cells has not yet been explored. It has been hypothesized that EP inhibits cancer cell growth. MCF-7 breast cancer cells, normal fibroblasts, and the non-transformed HEK-293 cell line were exposed to increasing concentrations of EP, and proliferation was assessed by the sulforhodamine-B assay. Results: MCF-7 cells exposed to EP were examined for cell cycle progression using flow cytometry, and DNA fragmentation was examined using the TUNEL assay. In addition, EP's mutagenic activity was assessed using the Salmonella typhimurium reverse mutation assay. The data showed that EP inhibits proliferation of MCF-7 cells, and it induces cell cycle arrest in G0/G1 through a DNA fragmentation-independent mechanism. Furthermore, EP's lack of overt cytotoxicity in the normal cell line HEK-293 and human fibroblasts in cell culture is supported by the absence of mutagenic activity of EP. Conclusion: EP emerges as a suitable molecule for further studies as a potential antineoplastic agent.info:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.52 20192019-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602019000100251en10.1186/s40659-019-0261-4
institution SCIELO
collection OJS
country Chile
countrycode CL
component Revista
access En linea
databasecode rev-scielo-cl
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Palacios-Moreno,Juan
Rubio,Cecilia
Quilhot,Wanda
Cavieres,M. Fernanda
Peña,Eduardo de la
Quiñones,Natalia V.
Díaz,Hugo
Carrión,Flavio
Henríquez-Roldán,Carlos F.
Weinstein-Oppenheimer,Caroline R.
spellingShingle Palacios-Moreno,Juan
Rubio,Cecilia
Quilhot,Wanda
Cavieres,M. Fernanda
Peña,Eduardo de la
Quiñones,Natalia V.
Díaz,Hugo
Carrión,Flavio
Henríquez-Roldán,Carlos F.
Weinstein-Oppenheimer,Caroline R.
Epanorin, a lichen secondary metabolite, inhibits proliferation of MCF-7 breast cancer cells
author_facet Palacios-Moreno,Juan
Rubio,Cecilia
Quilhot,Wanda
Cavieres,M. Fernanda
Peña,Eduardo de la
Quiñones,Natalia V.
Díaz,Hugo
Carrión,Flavio
Henríquez-Roldán,Carlos F.
Weinstein-Oppenheimer,Caroline R.
author_sort Palacios-Moreno,Juan
title Epanorin, a lichen secondary metabolite, inhibits proliferation of MCF-7 breast cancer cells
title_short Epanorin, a lichen secondary metabolite, inhibits proliferation of MCF-7 breast cancer cells
title_full Epanorin, a lichen secondary metabolite, inhibits proliferation of MCF-7 breast cancer cells
title_fullStr Epanorin, a lichen secondary metabolite, inhibits proliferation of MCF-7 breast cancer cells
title_full_unstemmed Epanorin, a lichen secondary metabolite, inhibits proliferation of MCF-7 breast cancer cells
title_sort epanorin, a lichen secondary metabolite, inhibits proliferation of mcf-7 breast cancer cells
description Abstract Background: Epanorin (EP) is a secondary metabolite of the Acarospora lichenic species. EP has been found in lichenic extracts with antimicrobial activity, and UV-absorption properties have been described for closely related molecules; however, its antiproliferative activity in cancer cells has not yet been explored. It has been hypothesized that EP inhibits cancer cell growth. MCF-7 breast cancer cells, normal fibroblasts, and the non-transformed HEK-293 cell line were exposed to increasing concentrations of EP, and proliferation was assessed by the sulforhodamine-B assay. Results: MCF-7 cells exposed to EP were examined for cell cycle progression using flow cytometry, and DNA fragmentation was examined using the TUNEL assay. In addition, EP's mutagenic activity was assessed using the Salmonella typhimurium reverse mutation assay. The data showed that EP inhibits proliferation of MCF-7 cells, and it induces cell cycle arrest in G0/G1 through a DNA fragmentation-independent mechanism. Furthermore, EP's lack of overt cytotoxicity in the normal cell line HEK-293 and human fibroblasts in cell culture is supported by the absence of mutagenic activity of EP. Conclusion: EP emerges as a suitable molecule for further studies as a potential antineoplastic agent.
publisher Sociedad de Biología de Chile
publishDate 2019
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602019000100251
work_keys_str_mv AT palaciosmorenojuan epanorinalichensecondarymetaboliteinhibitsproliferationofmcf7breastcancercells
AT rubiocecilia epanorinalichensecondarymetaboliteinhibitsproliferationofmcf7breastcancercells
AT quilhotwanda epanorinalichensecondarymetaboliteinhibitsproliferationofmcf7breastcancercells
AT cavieresmfernanda epanorinalichensecondarymetaboliteinhibitsproliferationofmcf7breastcancercells
AT penaeduardodela epanorinalichensecondarymetaboliteinhibitsproliferationofmcf7breastcancercells
AT quinonesnataliav epanorinalichensecondarymetaboliteinhibitsproliferationofmcf7breastcancercells
AT diazhugo epanorinalichensecondarymetaboliteinhibitsproliferationofmcf7breastcancercells
AT carrionflavio epanorinalichensecondarymetaboliteinhibitsproliferationofmcf7breastcancercells
AT henriquezroldancarlosf epanorinalichensecondarymetaboliteinhibitsproliferationofmcf7breastcancercells
AT weinsteinoppenheimercaroliner epanorinalichensecondarymetaboliteinhibitsproliferationofmcf7breastcancercells
_version_ 1755990968247517184