The genotoxic potential of alugbati leaf extracts on MCF-7 cells

To determine the genotoxicity of alugbati (Basella alba Linn. var. rubra) leaf extracts on breast adenocarcinoma, the Comet assay was employed on MCF-7 cells incubated with the following: lyophilized alugbati juice extracts reconstituted with 2 % DMSO (AJ) and in aqueous media (AJ2), and lyophilized...

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Main Authors: Garza, Darcy L., Arcilla, Rechel G., Enriquez, Ma Luisa D., Tan, Maria Carmen S., Noel, Marissa G.
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Published: Animo Repository 2019
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Online Access:https://animorepository.dlsu.edu.ph/faculty_research/1610
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Institution: De La Salle University
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spelling oai:animorepository.dlsu.edu.ph:faculty_research-26092021-07-07T07:13:30Z The genotoxic potential of alugbati leaf extracts on MCF-7 cells Garza, Darcy L. Arcilla, Rechel G. Enriquez, Ma Luisa D. Tan, Maria Carmen S. Noel, Marissa G. To determine the genotoxicity of alugbati (Basella alba Linn. var. rubra) leaf extracts on breast adenocarcinoma, the Comet assay was employed on MCF-7 cells incubated with the following: lyophilized alugbati juice extracts reconstituted with 2 % DMSO (AJ) and in aqueous media (AJ2), and lyophilized alugbati hydrolysate (exogenous myrosinase (E.C. 3.2.3.1) assisted) re- dissolved with 2 % DMSO in culture media (AH). Untreated MCF-7 cells in 2 % DMSO served as the negative control. MANOVA and Post hoc Tukey's HSD were employed to determine statistically significant differences among the samples. First, mutant cells in AJ and AH formed pronounced comet tails indicating that DNA damage had occurred significantly compared to that of the control. Post hoc comparisons between AJ and AH indicated that both samples exhibited comparable effects to MCF-7 cells. Due to the similarity of AJ to AH, it was presumed that hydrolysis occurred during the mechanical process of juice extraction. Second, AJ2 exhibited analogous results with the control; whereas, AJ was found to be statistically different. Aberrant cells incubated with the control and AJ2 trials exhibited relatively minimal genotoxicity as evidenced by intact nuclei. Overall, multiple comparisons illustrated that the most prominent DNA damage was observed by extracts AJ and AH in all parameters. The results of this study suggested that alugbati leaves subjected to enzyme-assisted hydrolysis or juice extractions prepared in DMSO caused considerable DNA damage in MCF-7 cells. © 2019 Jordan Journal of Biological Sciences. 2019-06-01T07:00:00Z text https://animorepository.dlsu.edu.ph/faculty_research/1610 Faculty Research Work Animo Repository Basellaceae—Toxicology Genetic toxicology Chemistry
institution De La Salle University
building De La Salle University Library
continent Asia
country Philippines
Philippines
content_provider De La Salle University Library
collection DLSU Institutional Repository
topic Basellaceae—Toxicology
Genetic toxicology
Chemistry
spellingShingle Basellaceae—Toxicology
Genetic toxicology
Chemistry
Garza, Darcy L.
Arcilla, Rechel G.
Enriquez, Ma Luisa D.
Tan, Maria Carmen S.
Noel, Marissa G.
The genotoxic potential of alugbati leaf extracts on MCF-7 cells
description To determine the genotoxicity of alugbati (Basella alba Linn. var. rubra) leaf extracts on breast adenocarcinoma, the Comet assay was employed on MCF-7 cells incubated with the following: lyophilized alugbati juice extracts reconstituted with 2 % DMSO (AJ) and in aqueous media (AJ2), and lyophilized alugbati hydrolysate (exogenous myrosinase (E.C. 3.2.3.1) assisted) re- dissolved with 2 % DMSO in culture media (AH). Untreated MCF-7 cells in 2 % DMSO served as the negative control. MANOVA and Post hoc Tukey's HSD were employed to determine statistically significant differences among the samples. First, mutant cells in AJ and AH formed pronounced comet tails indicating that DNA damage had occurred significantly compared to that of the control. Post hoc comparisons between AJ and AH indicated that both samples exhibited comparable effects to MCF-7 cells. Due to the similarity of AJ to AH, it was presumed that hydrolysis occurred during the mechanical process of juice extraction. Second, AJ2 exhibited analogous results with the control; whereas, AJ was found to be statistically different. Aberrant cells incubated with the control and AJ2 trials exhibited relatively minimal genotoxicity as evidenced by intact nuclei. Overall, multiple comparisons illustrated that the most prominent DNA damage was observed by extracts AJ and AH in all parameters. The results of this study suggested that alugbati leaves subjected to enzyme-assisted hydrolysis or juice extractions prepared in DMSO caused considerable DNA damage in MCF-7 cells. © 2019 Jordan Journal of Biological Sciences.
format text
author Garza, Darcy L.
Arcilla, Rechel G.
Enriquez, Ma Luisa D.
Tan, Maria Carmen S.
Noel, Marissa G.
author_facet Garza, Darcy L.
Arcilla, Rechel G.
Enriquez, Ma Luisa D.
Tan, Maria Carmen S.
Noel, Marissa G.
author_sort Garza, Darcy L.
title The genotoxic potential of alugbati leaf extracts on MCF-7 cells
title_short The genotoxic potential of alugbati leaf extracts on MCF-7 cells
title_full The genotoxic potential of alugbati leaf extracts on MCF-7 cells
title_fullStr The genotoxic potential of alugbati leaf extracts on MCF-7 cells
title_full_unstemmed The genotoxic potential of alugbati leaf extracts on MCF-7 cells
title_sort genotoxic potential of alugbati leaf extracts on mcf-7 cells
publisher Animo Repository
publishDate 2019
url https://animorepository.dlsu.edu.ph/faculty_research/1610
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