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In vitro studies of the anticancer action of Tectaria cicutaria in human cancer cell lines: G(0)/G(1) p53-associated cell cycle arrest-Part I

OBJECTIVE: The rhizome of Tectaria cicutaria has been used in Indian traditional medicine for the treatment of various disorders. The objective of present investigation is to screen various extracts of the rhizomes of Tectaria cicutaria for anti-cancer activity and to investigate the mechanism invol...

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Autores principales: Karade, Preeti Gajendra, Jadhav, Namdeo Ramhari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174258/
https://www.ncbi.nlm.nih.gov/pubmed/30302326
http://dx.doi.org/10.1016/j.jtcme.2017.07.003
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author Karade, Preeti Gajendra
Jadhav, Namdeo Ramhari
author_facet Karade, Preeti Gajendra
Jadhav, Namdeo Ramhari
author_sort Karade, Preeti Gajendra
collection PubMed
description OBJECTIVE: The rhizome of Tectaria cicutaria has been used in Indian traditional medicine for the treatment of various disorders. The objective of present investigation is to screen various extracts of the rhizomes of Tectaria cicutaria for anti-cancer activity and to investigate the mechanism involved. MATERIALS AND METHODS: The rhizomes of Tectaria cicutaria were extracted with different solvents. In vitro anti-cancer activity of different rhizome extracts were studied in Human cancer Cell Lines using Sulphorodamine B (SRB) colorimetric cytotoxicity assay. The effect of ethanolic extract (TCe) on cell growth inhibition, modulation in gene expression, and induction of apoptosis using the K562 human leukemia cell line were studied. The extract was analyzed by GC-MS to identify their major chemical compounds. RESULTS: TCe shows antioxidant potential in both DPPH scavenging assay and reducing capacity. Flow cytometric analysis showed that 11 μg/ml of TCe arrested cell cycle progression at the G(0)/G(1) phase. In the TCe treated K562 cells, the mRNA and protein expression level of p53 was strongly up-regulated in reverse transcription polymerase chain reaction. Furthermore, its downstream target p21 level was also increased. The GC-MS study has depicted results with the presence of twelve different compounds which will require significant further efforts for structure and putative identification. CONCLUSION: The present work has for the first time, tried to elucidate the anti leukemic potential of Tectaria cicutaria. TCe was more potent in K562 cells, altering the cell cycle progression and inducing apoptosis.
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spelling pubmed-61742582018-10-09 In vitro studies of the anticancer action of Tectaria cicutaria in human cancer cell lines: G(0)/G(1) p53-associated cell cycle arrest-Part I Karade, Preeti Gajendra Jadhav, Namdeo Ramhari J Tradit Complement Med Original Article OBJECTIVE: The rhizome of Tectaria cicutaria has been used in Indian traditional medicine for the treatment of various disorders. The objective of present investigation is to screen various extracts of the rhizomes of Tectaria cicutaria for anti-cancer activity and to investigate the mechanism involved. MATERIALS AND METHODS: The rhizomes of Tectaria cicutaria were extracted with different solvents. In vitro anti-cancer activity of different rhizome extracts were studied in Human cancer Cell Lines using Sulphorodamine B (SRB) colorimetric cytotoxicity assay. The effect of ethanolic extract (TCe) on cell growth inhibition, modulation in gene expression, and induction of apoptosis using the K562 human leukemia cell line were studied. The extract was analyzed by GC-MS to identify their major chemical compounds. RESULTS: TCe shows antioxidant potential in both DPPH scavenging assay and reducing capacity. Flow cytometric analysis showed that 11 μg/ml of TCe arrested cell cycle progression at the G(0)/G(1) phase. In the TCe treated K562 cells, the mRNA and protein expression level of p53 was strongly up-regulated in reverse transcription polymerase chain reaction. Furthermore, its downstream target p21 level was also increased. The GC-MS study has depicted results with the presence of twelve different compounds which will require significant further efforts for structure and putative identification. CONCLUSION: The present work has for the first time, tried to elucidate the anti leukemic potential of Tectaria cicutaria. TCe was more potent in K562 cells, altering the cell cycle progression and inducing apoptosis. Elsevier 2017-07-26 /pmc/articles/PMC6174258/ /pubmed/30302326 http://dx.doi.org/10.1016/j.jtcme.2017.07.003 Text en © 2017 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Karade, Preeti Gajendra
Jadhav, Namdeo Ramhari
In vitro studies of the anticancer action of Tectaria cicutaria in human cancer cell lines: G(0)/G(1) p53-associated cell cycle arrest-Part I
title In vitro studies of the anticancer action of Tectaria cicutaria in human cancer cell lines: G(0)/G(1) p53-associated cell cycle arrest-Part I
title_full In vitro studies of the anticancer action of Tectaria cicutaria in human cancer cell lines: G(0)/G(1) p53-associated cell cycle arrest-Part I
title_fullStr In vitro studies of the anticancer action of Tectaria cicutaria in human cancer cell lines: G(0)/G(1) p53-associated cell cycle arrest-Part I
title_full_unstemmed In vitro studies of the anticancer action of Tectaria cicutaria in human cancer cell lines: G(0)/G(1) p53-associated cell cycle arrest-Part I
title_short In vitro studies of the anticancer action of Tectaria cicutaria in human cancer cell lines: G(0)/G(1) p53-associated cell cycle arrest-Part I
title_sort in vitro studies of the anticancer action of tectaria cicutaria in human cancer cell lines: g(0)/g(1) p53-associated cell cycle arrest-part i
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174258/
https://www.ncbi.nlm.nih.gov/pubmed/30302326
http://dx.doi.org/10.1016/j.jtcme.2017.07.003
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