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Antitumor Activity of Noscapine in Combination with Doxorubicin in Triple Negative Breast Cancer

BACKGROUND: The aim of this study was to investigate the anticancer activity and mechanism of action of Noscapine alone and in combination with Doxorubicin against triple negative breast cancer (TNBC). METHODS: TNBC cells were pretreated with Noscapine or Doxorubicin or combination and combination i...

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Autores principales: Chougule, Mahavir B., Patel, Apurva R., Jackson, Tanise, Singh, Mandip
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3057970/
https://www.ncbi.nlm.nih.gov/pubmed/21423660
http://dx.doi.org/10.1371/journal.pone.0017733
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author Chougule, Mahavir B.
Patel, Apurva R.
Jackson, Tanise
Singh, Mandip
author_facet Chougule, Mahavir B.
Patel, Apurva R.
Jackson, Tanise
Singh, Mandip
author_sort Chougule, Mahavir B.
collection PubMed
description BACKGROUND: The aim of this study was to investigate the anticancer activity and mechanism of action of Noscapine alone and in combination with Doxorubicin against triple negative breast cancer (TNBC). METHODS: TNBC cells were pretreated with Noscapine or Doxorubicin or combination and combination index values were calculated using isobolographic method. Apoptosis was assessed by TUNEL staining. Female athymic Nu/nu mice were xenografted with MDA-MB-231 cells and the efficacy of Noscapine, Doxorubicin and combination was determined. Protein expression, immunohistochemical staining were evaluated in harvested tumor tissues. RESULTS: Noscapine inhibited growth of MDA-MB-231 and MDA-MB-468 cells with the IC(50) values of 36.16±3.76 and 42.7±4.3 µM respectively. The CI values (<0.59) were suggestive of strong synergistic interaction between Noscapine and Doxorubicin and combination treatment showed significant increase in apoptotic cells. Noscapine showed dose dependent reduction in the tumor volumes at a dose of 150–550 mg/kg/day compared to controls. Noscapine (300 mg/kg), Doxorubicin (1.5 mg/kg) and combination treatment reduced tumor volume by 39.4±5.8, 34.2±5.7 and 82.9±4.5 percent respectively and showed decreased expression of NF-KB pathway proteins, VEGF, cell survival, and increased expression of apoptotic and growth inhibitory proteins compared to single-agent treatment and control groups. CONCLUSIONS: Noscapine potentiated the anticancer activity of Doxorubicin in a synergistic manner against TNBC tumors via inactivation of NF-KB and anti-angiogenic pathways while stimulating apoptosis. These findings suggest potential benefit for use of oral Noscapine and Doxorubicin combination therapy for treatment of more aggressive TNBC.
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spelling pubmed-30579702011-03-21 Antitumor Activity of Noscapine in Combination with Doxorubicin in Triple Negative Breast Cancer Chougule, Mahavir B. Patel, Apurva R. Jackson, Tanise Singh, Mandip PLoS One Research Article BACKGROUND: The aim of this study was to investigate the anticancer activity and mechanism of action of Noscapine alone and in combination with Doxorubicin against triple negative breast cancer (TNBC). METHODS: TNBC cells were pretreated with Noscapine or Doxorubicin or combination and combination index values were calculated using isobolographic method. Apoptosis was assessed by TUNEL staining. Female athymic Nu/nu mice were xenografted with MDA-MB-231 cells and the efficacy of Noscapine, Doxorubicin and combination was determined. Protein expression, immunohistochemical staining were evaluated in harvested tumor tissues. RESULTS: Noscapine inhibited growth of MDA-MB-231 and MDA-MB-468 cells with the IC(50) values of 36.16±3.76 and 42.7±4.3 µM respectively. The CI values (<0.59) were suggestive of strong synergistic interaction between Noscapine and Doxorubicin and combination treatment showed significant increase in apoptotic cells. Noscapine showed dose dependent reduction in the tumor volumes at a dose of 150–550 mg/kg/day compared to controls. Noscapine (300 mg/kg), Doxorubicin (1.5 mg/kg) and combination treatment reduced tumor volume by 39.4±5.8, 34.2±5.7 and 82.9±4.5 percent respectively and showed decreased expression of NF-KB pathway proteins, VEGF, cell survival, and increased expression of apoptotic and growth inhibitory proteins compared to single-agent treatment and control groups. CONCLUSIONS: Noscapine potentiated the anticancer activity of Doxorubicin in a synergistic manner against TNBC tumors via inactivation of NF-KB and anti-angiogenic pathways while stimulating apoptosis. These findings suggest potential benefit for use of oral Noscapine and Doxorubicin combination therapy for treatment of more aggressive TNBC. Public Library of Science 2011-03-15 /pmc/articles/PMC3057970/ /pubmed/21423660 http://dx.doi.org/10.1371/journal.pone.0017733 Text en Chougule et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chougule, Mahavir B.
Patel, Apurva R.
Jackson, Tanise
Singh, Mandip
Antitumor Activity of Noscapine in Combination with Doxorubicin in Triple Negative Breast Cancer
title Antitumor Activity of Noscapine in Combination with Doxorubicin in Triple Negative Breast Cancer
title_full Antitumor Activity of Noscapine in Combination with Doxorubicin in Triple Negative Breast Cancer
title_fullStr Antitumor Activity of Noscapine in Combination with Doxorubicin in Triple Negative Breast Cancer
title_full_unstemmed Antitumor Activity of Noscapine in Combination with Doxorubicin in Triple Negative Breast Cancer
title_short Antitumor Activity of Noscapine in Combination with Doxorubicin in Triple Negative Breast Cancer
title_sort antitumor activity of noscapine in combination with doxorubicin in triple negative breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3057970/
https://www.ncbi.nlm.nih.gov/pubmed/21423660
http://dx.doi.org/10.1371/journal.pone.0017733
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