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An In Vitro Estimation of the Cytotoxicity and Genotoxicity of Root Extract from Leonurus sibiricus L. Overexpressing AtPAP1 against Different Cancer Cell Lines
As the current cancer treatment success rate is not sufficient, interest has grown in plants as possible sources of anti-cancer compounds. One such plant with a broad spectrum of activity is of the family Lamiaceae. This study investigates for the first time both the genotoxic and cytotoxic activiti...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2018-08, Vol.23 (8), p.2049 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | As the current cancer treatment success rate is not sufficient, interest has grown in plants as possible sources of anti-cancer compounds. One such plant with a broad spectrum of activity is
of the family Lamiaceae. This study investigates for the first time both the genotoxic and cytotoxic activities of TR (transformed) and AtPAP1 TR (with over-expression of transcriptional factor) root extracts of
against various cancer cell lines (CCRF-CEM, K-562 and A549). Both tested extracts showed a cytotoxic effect on CCRF-CEM and K-562 cell lines, but strongest activity was observed for the AtPAP1 TR extract. No cytotoxic effect was observed against the A549 cell line in the tested concentration range, and it was found that both tested extracts may induce apoptosis by decreasing mitochondrial membrane potential and inducing nDNA damage lesion in the
region and mtDNA in
(mitochondrially encoded NADH: ubiquinone oxidoreductase core subunit 1) and
(mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5) regions in K-562 and CCRF-CEM. Our results confirmed that TR and AtPAP1 TR root extracts from
are cytotoxic and genotoxic against different model cell lines (CCRF-CEM and K-562)
However, the observed genotoxicity of both extracts needs to be confirmed by additional studies. These preclinical observations support the use of
with other pharmacological purposes. |
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ISSN: | 1420-3049 1420-3049 |
DOI: | 10.3390/molecules23082049 |