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In Vitro Anticancer Effect of Gedunin on Human Teratocarcinomal (NTERA-2) Cancer Stem-Like Cells
Gedunin is one of the major compounds found in the neem tree (Azadirachta indica). In the present study, antiproliferative potential of gedunin was evaluated in human embryonal carcinoma cells (NTERA-2, a cancer stem cell model) and peripheral blood mononuclear cells (PBMCs), using Sulforhodamine (S...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478822/ https://www.ncbi.nlm.nih.gov/pubmed/28680880 http://dx.doi.org/10.1155/2017/2413197 |
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author | Tharmarajah, Luxmiga Samarakoon, Sameera Ranganath Ediriweera, Meran Keshawa Piyathilaka, Poorna Tennekoon, Kamani Hemamamla Senathilake, Kanishka Sithira Rajagopalan, Umapriyatharshini Galhena, Prasanna Bandula Thabrew, Ira |
author_facet | Tharmarajah, Luxmiga Samarakoon, Sameera Ranganath Ediriweera, Meran Keshawa Piyathilaka, Poorna Tennekoon, Kamani Hemamamla Senathilake, Kanishka Sithira Rajagopalan, Umapriyatharshini Galhena, Prasanna Bandula Thabrew, Ira |
author_sort | Tharmarajah, Luxmiga |
collection | PubMed |
description | Gedunin is one of the major compounds found in the neem tree (Azadirachta indica). In the present study, antiproliferative potential of gedunin was evaluated in human embryonal carcinoma cells (NTERA-2, a cancer stem cell model) and peripheral blood mononuclear cells (PBMCs), using Sulforhodamine (SRB) and WST-1 assays, respectively. The effects of gedunin on expression of heat shock protein 90 (HSP90), its cochaperone Cdc37, and HSP client proteins (AKT, ErbB2, and HSF1) were evaluated by real-time PCR. Effects of gedunin on apoptosis were evaluated by (a) apoptosis associated morphological changes, (b) caspase 3/7 expression, (c) DNA fragmentation, (d) TUNEL assay, and (e) real-time PCR of apoptosis related genes (Bax, p53, and survivin). Gedunin showed a promising antiproliferative effect in NTERA-2 cells with IC(50) values of 14.59, 8.49, and 6.55 μg/mL at 24, 48, and 72 h after incubations, respectively, while exerting a minimal effect on PBMCs. Expression of HSP90, its client proteins, and survivin was inhibited and Bax and p53 were upregulated by gedunin. Apoptosis related morphological changes, DNA fragmentation, and increased caspase 3/7 activities confirmed the proapoptotic effects of gedunin. Collectively, results indicate that gedunin may be a good drug lead for treatment of chemo and radiotherapy resistant cancer stem cells. |
format | Online Article Text |
id | pubmed-5478822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-54788222017-07-05 In Vitro Anticancer Effect of Gedunin on Human Teratocarcinomal (NTERA-2) Cancer Stem-Like Cells Tharmarajah, Luxmiga Samarakoon, Sameera Ranganath Ediriweera, Meran Keshawa Piyathilaka, Poorna Tennekoon, Kamani Hemamamla Senathilake, Kanishka Sithira Rajagopalan, Umapriyatharshini Galhena, Prasanna Bandula Thabrew, Ira Biomed Res Int Research Article Gedunin is one of the major compounds found in the neem tree (Azadirachta indica). In the present study, antiproliferative potential of gedunin was evaluated in human embryonal carcinoma cells (NTERA-2, a cancer stem cell model) and peripheral blood mononuclear cells (PBMCs), using Sulforhodamine (SRB) and WST-1 assays, respectively. The effects of gedunin on expression of heat shock protein 90 (HSP90), its cochaperone Cdc37, and HSP client proteins (AKT, ErbB2, and HSF1) were evaluated by real-time PCR. Effects of gedunin on apoptosis were evaluated by (a) apoptosis associated morphological changes, (b) caspase 3/7 expression, (c) DNA fragmentation, (d) TUNEL assay, and (e) real-time PCR of apoptosis related genes (Bax, p53, and survivin). Gedunin showed a promising antiproliferative effect in NTERA-2 cells with IC(50) values of 14.59, 8.49, and 6.55 μg/mL at 24, 48, and 72 h after incubations, respectively, while exerting a minimal effect on PBMCs. Expression of HSP90, its client proteins, and survivin was inhibited and Bax and p53 were upregulated by gedunin. Apoptosis related morphological changes, DNA fragmentation, and increased caspase 3/7 activities confirmed the proapoptotic effects of gedunin. Collectively, results indicate that gedunin may be a good drug lead for treatment of chemo and radiotherapy resistant cancer stem cells. Hindawi 2017 2017-06-07 /pmc/articles/PMC5478822/ /pubmed/28680880 http://dx.doi.org/10.1155/2017/2413197 Text en Copyright © 2017 Luxmiga Tharmarajah et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Tharmarajah, Luxmiga Samarakoon, Sameera Ranganath Ediriweera, Meran Keshawa Piyathilaka, Poorna Tennekoon, Kamani Hemamamla Senathilake, Kanishka Sithira Rajagopalan, Umapriyatharshini Galhena, Prasanna Bandula Thabrew, Ira In Vitro Anticancer Effect of Gedunin on Human Teratocarcinomal (NTERA-2) Cancer Stem-Like Cells |
title | In Vitro Anticancer Effect of Gedunin on Human Teratocarcinomal (NTERA-2) Cancer Stem-Like Cells |
title_full | In Vitro Anticancer Effect of Gedunin on Human Teratocarcinomal (NTERA-2) Cancer Stem-Like Cells |
title_fullStr | In Vitro Anticancer Effect of Gedunin on Human Teratocarcinomal (NTERA-2) Cancer Stem-Like Cells |
title_full_unstemmed | In Vitro Anticancer Effect of Gedunin on Human Teratocarcinomal (NTERA-2) Cancer Stem-Like Cells |
title_short | In Vitro Anticancer Effect of Gedunin on Human Teratocarcinomal (NTERA-2) Cancer Stem-Like Cells |
title_sort | in vitro anticancer effect of gedunin on human teratocarcinomal (ntera-2) cancer stem-like cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478822/ https://www.ncbi.nlm.nih.gov/pubmed/28680880 http://dx.doi.org/10.1155/2017/2413197 |
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