Antitumor activity of new chemical compounds in triple negative mammary adenocarcinoma models

Aim: According to the need for the development of new anticancer agents, we have synthetized novel bioactive compounds and aimed to determine their antitumor action. Materials & methods: We describe in vitro studies evaluating the effect of 35 novel chemical compounds on two triple negative muri...

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Autores principales: Giolito, Maria Virginia, Camacho, Cristian M., Martinez-Amezaga, Maitena, Traficante, Carla Inés, Giordano, Rocío A., Cornier, Patricia G., Mata, Ernesto G., Delpiccolo, Carina M.L., Boggián, Dora G., Del Giúdice, Antonela, Mainetti, Leandro Ernesto, Scharovsky, Olga Graciela, Rozados, Viviana R., Rico, María José
Formato: article artículo publishedVersion
Lenguaje:Inglés
Publicado: Future Science Group 2020
Materias:
Acceso en línea:http://hdl.handle.net/2133/19381
http://hdl.handle.net/2133/19381
Aporte de:
id I15-R121-2133-19381
record_format dspace
institution Universidad Nacional de Rosario
institution_str I-15
repository_str R-121
collection Repositorio Hipermedial de la Universidad Nacional de Rosario (UNR)
language Inglés
orig_language_str_mv eng
topic Antitumor effect
Chemical agents
In vitro assays
Triple negative mammary adenocarcinoma
spellingShingle Antitumor effect
Chemical agents
In vitro assays
Triple negative mammary adenocarcinoma
Giolito, Maria Virginia
Camacho, Cristian M.
Martinez-Amezaga, Maitena
Traficante, Carla Inés
Giordano, Rocío A.
Cornier, Patricia G.
Mata, Ernesto G.
Delpiccolo, Carina M.L.
Boggián, Dora G.
Del Giúdice, Antonela
Mainetti, Leandro Ernesto
Scharovsky, Olga Graciela
Rozados, Viviana R.
Rico, María José
Antitumor activity of new chemical compounds in triple negative mammary adenocarcinoma models
topic_facet Antitumor effect
Chemical agents
In vitro assays
Triple negative mammary adenocarcinoma
description Aim: According to the need for the development of new anticancer agents, we have synthetized novel bioactive compounds and aimed to determine their antitumor action. Materials & methods: We describe in vitro studies evaluating the effect of 35 novel chemical compounds on two triple negative murine mammary adenocarcinoma tumors. Results & conclusion: Three compounds were selected because of their high antitumor activity and their low toxicity to normal cells. Their effect on tumor cells apoptosis, clonogenicity and migratory capacity, were determined. We found that the selected compounds showed inhibition of viability and clonogenic capacity, and promotion of apoptosis. They also decreased the migratory capacity of tumor cells. The results obtained suggest the likelihood of their future use as antitumor and/or antimetastatic agents.
format article
artículo
publishedVersion
author Giolito, Maria Virginia
Camacho, Cristian M.
Martinez-Amezaga, Maitena
Traficante, Carla Inés
Giordano, Rocío A.
Cornier, Patricia G.
Mata, Ernesto G.
Delpiccolo, Carina M.L.
Boggián, Dora G.
Del Giúdice, Antonela
Mainetti, Leandro Ernesto
Scharovsky, Olga Graciela
Rozados, Viviana R.
Rico, María José
author_facet Giolito, Maria Virginia
Camacho, Cristian M.
Martinez-Amezaga, Maitena
Traficante, Carla Inés
Giordano, Rocío A.
Cornier, Patricia G.
Mata, Ernesto G.
Delpiccolo, Carina M.L.
Boggián, Dora G.
Del Giúdice, Antonela
Mainetti, Leandro Ernesto
Scharovsky, Olga Graciela
Rozados, Viviana R.
Rico, María José
author_sort Giolito, Maria Virginia
title Antitumor activity of new chemical compounds in triple negative mammary adenocarcinoma models
title_short Antitumor activity of new chemical compounds in triple negative mammary adenocarcinoma models
title_full Antitumor activity of new chemical compounds in triple negative mammary adenocarcinoma models
title_fullStr Antitumor activity of new chemical compounds in triple negative mammary adenocarcinoma models
title_full_unstemmed Antitumor activity of new chemical compounds in triple negative mammary adenocarcinoma models
title_sort antitumor activity of new chemical compounds in triple negative mammary adenocarcinoma models
publisher Future Science Group
publishDate 2020
url http://hdl.handle.net/2133/19381
http://hdl.handle.net/2133/19381
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