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Mechanism of Action of the Novel Nickel(II) Complex in Simultaneous Reactivation of the Apoptotic Signaling Networks Against Human Colon Cancer Cells

The aim of this study was to evaluate the cytotoxic potential of a novel nickel(II) complex (NTC) against WiDr and HT-29 human colon cancer cells by determining the IC(50) using the standard MTT assay. The NTC displayed a strong suppressive effect on colon cancer cells with an IC(50) value of 6.07 ±...

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Autores principales: Samie, Nima, Haerian, Batoul Sadat, Muniandy, Sekaran, Marlina, Anita, Kanthimathi, M. S., Abdullah, Norbani B., Ahmadian, Gholamreza, Aziddin, Raja E. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729910/
https://www.ncbi.nlm.nih.gov/pubmed/26858642
http://dx.doi.org/10.3389/fphar.2015.00313
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author Samie, Nima
Haerian, Batoul Sadat
Muniandy, Sekaran
Marlina, Anita
Kanthimathi, M. S.
Abdullah, Norbani B.
Ahmadian, Gholamreza
Aziddin, Raja E. R.
author_facet Samie, Nima
Haerian, Batoul Sadat
Muniandy, Sekaran
Marlina, Anita
Kanthimathi, M. S.
Abdullah, Norbani B.
Ahmadian, Gholamreza
Aziddin, Raja E. R.
author_sort Samie, Nima
collection PubMed
description The aim of this study was to evaluate the cytotoxic potential of a novel nickel(II) complex (NTC) against WiDr and HT-29 human colon cancer cells by determining the IC(50) using the standard MTT assay. The NTC displayed a strong suppressive effect on colon cancer cells with an IC(50) value of 6.07 ± 0.22 μM and 6.26 ± 0.13 μM against WiDr and HT-29 respectively, after 24 h of treatment. Substantial reduction in the mitochondrial membrane potential and increase in the release of cytochrome c from the mitochondria directed the induction of the intrinsic apoptosis pathway by the NTC. Activation of this pathway was further evidenced by significant activation of caspase 3/7 and 9. The NTC was also shown to activate the extrinsic pathway of apoptosis via activation of caspase-8 which is linked to the suppression of NF-κB translocation to the nucleus. Cell cycle arrest in the G1 phase was confirmed by flow cytometry and up-regulation of glutathione reductase expression was quantified by qPCR. Results of the current work indicates that NTC possess a potent cancer cell abolishing activity by simultaneous induction of intrinsic and extrinsic pathways of apoptosis in colon cancer cell lines.
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spelling pubmed-47299102016-02-08 Mechanism of Action of the Novel Nickel(II) Complex in Simultaneous Reactivation of the Apoptotic Signaling Networks Against Human Colon Cancer Cells Samie, Nima Haerian, Batoul Sadat Muniandy, Sekaran Marlina, Anita Kanthimathi, M. S. Abdullah, Norbani B. Ahmadian, Gholamreza Aziddin, Raja E. R. Front Pharmacol Pharmacology The aim of this study was to evaluate the cytotoxic potential of a novel nickel(II) complex (NTC) against WiDr and HT-29 human colon cancer cells by determining the IC(50) using the standard MTT assay. The NTC displayed a strong suppressive effect on colon cancer cells with an IC(50) value of 6.07 ± 0.22 μM and 6.26 ± 0.13 μM against WiDr and HT-29 respectively, after 24 h of treatment. Substantial reduction in the mitochondrial membrane potential and increase in the release of cytochrome c from the mitochondria directed the induction of the intrinsic apoptosis pathway by the NTC. Activation of this pathway was further evidenced by significant activation of caspase 3/7 and 9. The NTC was also shown to activate the extrinsic pathway of apoptosis via activation of caspase-8 which is linked to the suppression of NF-κB translocation to the nucleus. Cell cycle arrest in the G1 phase was confirmed by flow cytometry and up-regulation of glutathione reductase expression was quantified by qPCR. Results of the current work indicates that NTC possess a potent cancer cell abolishing activity by simultaneous induction of intrinsic and extrinsic pathways of apoptosis in colon cancer cell lines. Frontiers Media S.A. 2016-01-28 /pmc/articles/PMC4729910/ /pubmed/26858642 http://dx.doi.org/10.3389/fphar.2015.00313 Text en Copyright © 2016 Samie, Haerian, Muniandy, Marlina, Kanthimathi, Abdullah, Ahmadian and Aziddin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Samie, Nima
Haerian, Batoul Sadat
Muniandy, Sekaran
Marlina, Anita
Kanthimathi, M. S.
Abdullah, Norbani B.
Ahmadian, Gholamreza
Aziddin, Raja E. R.
Mechanism of Action of the Novel Nickel(II) Complex in Simultaneous Reactivation of the Apoptotic Signaling Networks Against Human Colon Cancer Cells
title Mechanism of Action of the Novel Nickel(II) Complex in Simultaneous Reactivation of the Apoptotic Signaling Networks Against Human Colon Cancer Cells
title_full Mechanism of Action of the Novel Nickel(II) Complex in Simultaneous Reactivation of the Apoptotic Signaling Networks Against Human Colon Cancer Cells
title_fullStr Mechanism of Action of the Novel Nickel(II) Complex in Simultaneous Reactivation of the Apoptotic Signaling Networks Against Human Colon Cancer Cells
title_full_unstemmed Mechanism of Action of the Novel Nickel(II) Complex in Simultaneous Reactivation of the Apoptotic Signaling Networks Against Human Colon Cancer Cells
title_short Mechanism of Action of the Novel Nickel(II) Complex in Simultaneous Reactivation of the Apoptotic Signaling Networks Against Human Colon Cancer Cells
title_sort mechanism of action of the novel nickel(ii) complex in simultaneous reactivation of the apoptotic signaling networks against human colon cancer cells
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729910/
https://www.ncbi.nlm.nih.gov/pubmed/26858642
http://dx.doi.org/10.3389/fphar.2015.00313
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