Nordamnacanthal induced apoptosis and mitotic-G2/M arrest with downregulation of Bcl-2 in the human breast cancer cell line (MCF-7).

Nordamnacanthal, an anthraquinone extracted from the root of Morindaelliptica from Rubiaceae family has cytotoxic properties towards cancer cell lines and anti tumor promoting activities. This study was conducted to determine the cytotoxic effect of nordamnacanthal towards MOLT-4 and MCF-7 cell line...

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Main Authors: Ishak , Norsyafini, Saiful Yazan , Latifah, Lajis, Nordin
Format: Article
Language:English
English
Published: Prague Development Center. 2010
Online Access:http://psasir.upm.edu.my/id/eprint/15834/1/Nordamnacanthal%20induced%20apoptosis%20and%20mitotic.pdf
http://psasir.upm.edu.my/id/eprint/15834/
http://www.pradec.eu/
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spelling my.upm.eprints.158342015-09-28T08:14:58Z http://psasir.upm.edu.my/id/eprint/15834/ Nordamnacanthal induced apoptosis and mitotic-G2/M arrest with downregulation of Bcl-2 in the human breast cancer cell line (MCF-7). Ishak , Norsyafini Saiful Yazan , Latifah Lajis, Nordin Nordamnacanthal, an anthraquinone extracted from the root of Morindaelliptica from Rubiaceae family has cytotoxic properties towards cancer cell lines and anti tumor promoting activities. This study was conducted to determine the cytotoxic effect of nordamnacanthal towards MOLT-4 and MCF-7 cell lines. Nordamnacanthal was found to be more cytotoxic towards MOLT-4 than MCF-7 with the IC50 of 3.8 μg/ml and 54μg/ml, respectively, as detected by using the trypan blue dye exclusion test. The nordamnacanthal-treated cells showed characteristics of apoptosis such as membrane blebbing, chromatin condensation and formation of apoptotic bodies as observed under an inverted lightmicroscope. Fluorescence analysis of cell death using acridine orange and propidium iodide staining showed that the population of MOLT-4 and MCF-7 cells underwent apoptosis at the IC50 value was 32% and 30.4%,respectively. Cell cycle analysis by flow cytometry indicated that nordamnacanthal did arrest MCF-7 cells at the G2/M phase. For MOLT-4, no cell cycle arrest was observed. Bcl-2 and Bax were downregulated in nordamnacanthal-treated MCF-7 cells. On the other hand, expression of the proteins in MOLT-4 was not from the control. In conclusion, nordamnacanthal was more cytotoxic towards MOLT-4 than MCF-7 cell line. The compound induced apoptosis in both cell lines, but with G2/M arrest and the involvement of Bcl-2 and Bax only in MCF-7. Prague Development Center. 2010 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/15834/1/Nordamnacanthal%20induced%20apoptosis%20and%20mitotic.pdf Ishak , Norsyafini and Saiful Yazan , Latifah and Lajis, Nordin (2010) Nordamnacanthal induced apoptosis and mitotic-G2/M arrest with downregulation of Bcl-2 in the human breast cancer cell line (MCF-7). Medical and Health Science Journal, 2 (2). pp. 27-38. ISSN 1804-1884, ESSN : 1804-5014. http://www.pradec.eu/ English
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
English
description Nordamnacanthal, an anthraquinone extracted from the root of Morindaelliptica from Rubiaceae family has cytotoxic properties towards cancer cell lines and anti tumor promoting activities. This study was conducted to determine the cytotoxic effect of nordamnacanthal towards MOLT-4 and MCF-7 cell lines. Nordamnacanthal was found to be more cytotoxic towards MOLT-4 than MCF-7 with the IC50 of 3.8 μg/ml and 54μg/ml, respectively, as detected by using the trypan blue dye exclusion test. The nordamnacanthal-treated cells showed characteristics of apoptosis such as membrane blebbing, chromatin condensation and formation of apoptotic bodies as observed under an inverted lightmicroscope. Fluorescence analysis of cell death using acridine orange and propidium iodide staining showed that the population of MOLT-4 and MCF-7 cells underwent apoptosis at the IC50 value was 32% and 30.4%,respectively. Cell cycle analysis by flow cytometry indicated that nordamnacanthal did arrest MCF-7 cells at the G2/M phase. For MOLT-4, no cell cycle arrest was observed. Bcl-2 and Bax were downregulated in nordamnacanthal-treated MCF-7 cells. On the other hand, expression of the proteins in MOLT-4 was not from the control. In conclusion, nordamnacanthal was more cytotoxic towards MOLT-4 than MCF-7 cell line. The compound induced apoptosis in both cell lines, but with G2/M arrest and the involvement of Bcl-2 and Bax only in MCF-7.
format Article
author Ishak , Norsyafini
Saiful Yazan , Latifah
Lajis, Nordin
spellingShingle Ishak , Norsyafini
Saiful Yazan , Latifah
Lajis, Nordin
Nordamnacanthal induced apoptosis and mitotic-G2/M arrest with downregulation of Bcl-2 in the human breast cancer cell line (MCF-7).
author_facet Ishak , Norsyafini
Saiful Yazan , Latifah
Lajis, Nordin
author_sort Ishak , Norsyafini
title Nordamnacanthal induced apoptosis and mitotic-G2/M arrest with downregulation of Bcl-2 in the human breast cancer cell line (MCF-7).
title_short Nordamnacanthal induced apoptosis and mitotic-G2/M arrest with downregulation of Bcl-2 in the human breast cancer cell line (MCF-7).
title_full Nordamnacanthal induced apoptosis and mitotic-G2/M arrest with downregulation of Bcl-2 in the human breast cancer cell line (MCF-7).
title_fullStr Nordamnacanthal induced apoptosis and mitotic-G2/M arrest with downregulation of Bcl-2 in the human breast cancer cell line (MCF-7).
title_full_unstemmed Nordamnacanthal induced apoptosis and mitotic-G2/M arrest with downregulation of Bcl-2 in the human breast cancer cell line (MCF-7).
title_sort nordamnacanthal induced apoptosis and mitotic-g2/m arrest with downregulation of bcl-2 in the human breast cancer cell line (mcf-7).
publisher Prague Development Center.
publishDate 2010
url http://psasir.upm.edu.my/id/eprint/15834/1/Nordamnacanthal%20induced%20apoptosis%20and%20mitotic.pdf
http://psasir.upm.edu.my/id/eprint/15834/
http://www.pradec.eu/
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