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Antineoplastic activity of a nutrient mixture in Y-79 malignant retinoblastoma cells

Retinoblastoma is one of the most common ocular malignancies in children under the age of six. Occasionally, retinoblastoma metastasizes to extraocular organs including the bone, lung and brain. Left untreated, retinoblastoma is fatal. At present, there is no effective treatment for metastatic retin...

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Autores principales: ROOMI, M. WAHEED, ROOMI, NUSRATH, BHANAP, BILWA, NIEDZWIECKI, ALEKSANDRA, RATH, MATTHIAS
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583477/
https://www.ncbi.nlm.nih.gov/pubmed/23129147
http://dx.doi.org/10.3892/or.2012.2110
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author ROOMI, M. WAHEED
ROOMI, NUSRATH
BHANAP, BILWA
NIEDZWIECKI, ALEKSANDRA
RATH, MATTHIAS
author_facet ROOMI, M. WAHEED
ROOMI, NUSRATH
BHANAP, BILWA
NIEDZWIECKI, ALEKSANDRA
RATH, MATTHIAS
author_sort ROOMI, M. WAHEED
collection PubMed
description Retinoblastoma is one of the most common ocular malignancies in children under the age of six. Occasionally, retinoblastoma metastasizes to extraocular organs including the bone, lung and brain. Left untreated, retinoblastoma is fatal. At present, there is no effective treatment for metastatic retinoblastoma. We investigated the antineoplastic activity of a nutrient mixture (NM) (lysine, proline, ascorbic acid and green tea extract) at concentrations of 10, 50, 100, 500 and 1,000 μg/ml in triplicate at each dose in the human malignant retinoblastoma Y-79 cell line. The parameters used were cell proliferation, expression of matrix metalloproteinases (MMPs), invasion through Matrigel, morphology and apoptosis. Cell viability was assessed by trypan blue dye exclusion test. Invasion was evaluated through Matrigel and MMP activity by gelatinase zymography. H&E staining for morphological cell alterations and apoptotic studies using the Live Green Poly Caspase Detection kit were also conducted. The nutrient mixture at 10–100 μg/ml demonstrated approximately 25% toxicity towards Y-79 retinoblastoma cells and significant toxicity at 500 and 1,000 μg/ml. The Y-79 cells secreted only MMP-2 as demonstrated by zymography; the nutrient mixture had no effect on MMP-2 expression up to 100 μg/ml, but completely blocked it at 500 μg/ml. Importantly, Y-79 retinoblastoma cells were not invasive through Matrigel. H&E staining showed cell morphological changes related to apoptosis, which was confirmed using the Live Green Poly Caspase Detection kit. Our results suggest that this nutrient mixture, which inhibited cell proliferation, expression of MMP-2 and induced apoptosis, may be a candidate for further exploration for its therapeutic potential in metastatic retinoblastoma.
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spelling pubmed-35834772013-02-28 Antineoplastic activity of a nutrient mixture in Y-79 malignant retinoblastoma cells ROOMI, M. WAHEED ROOMI, NUSRATH BHANAP, BILWA NIEDZWIECKI, ALEKSANDRA RATH, MATTHIAS Oncol Rep Articles Retinoblastoma is one of the most common ocular malignancies in children under the age of six. Occasionally, retinoblastoma metastasizes to extraocular organs including the bone, lung and brain. Left untreated, retinoblastoma is fatal. At present, there is no effective treatment for metastatic retinoblastoma. We investigated the antineoplastic activity of a nutrient mixture (NM) (lysine, proline, ascorbic acid and green tea extract) at concentrations of 10, 50, 100, 500 and 1,000 μg/ml in triplicate at each dose in the human malignant retinoblastoma Y-79 cell line. The parameters used were cell proliferation, expression of matrix metalloproteinases (MMPs), invasion through Matrigel, morphology and apoptosis. Cell viability was assessed by trypan blue dye exclusion test. Invasion was evaluated through Matrigel and MMP activity by gelatinase zymography. H&E staining for morphological cell alterations and apoptotic studies using the Live Green Poly Caspase Detection kit were also conducted. The nutrient mixture at 10–100 μg/ml demonstrated approximately 25% toxicity towards Y-79 retinoblastoma cells and significant toxicity at 500 and 1,000 μg/ml. The Y-79 cells secreted only MMP-2 as demonstrated by zymography; the nutrient mixture had no effect on MMP-2 expression up to 100 μg/ml, but completely blocked it at 500 μg/ml. Importantly, Y-79 retinoblastoma cells were not invasive through Matrigel. H&E staining showed cell morphological changes related to apoptosis, which was confirmed using the Live Green Poly Caspase Detection kit. Our results suggest that this nutrient mixture, which inhibited cell proliferation, expression of MMP-2 and induced apoptosis, may be a candidate for further exploration for its therapeutic potential in metastatic retinoblastoma. D.A. Spandidos 2012-10-29 2013-01 /pmc/articles/PMC3583477/ /pubmed/23129147 http://dx.doi.org/10.3892/or.2012.2110 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
ROOMI, M. WAHEED
ROOMI, NUSRATH
BHANAP, BILWA
NIEDZWIECKI, ALEKSANDRA
RATH, MATTHIAS
Antineoplastic activity of a nutrient mixture in Y-79 malignant retinoblastoma cells
title Antineoplastic activity of a nutrient mixture in Y-79 malignant retinoblastoma cells
title_full Antineoplastic activity of a nutrient mixture in Y-79 malignant retinoblastoma cells
title_fullStr Antineoplastic activity of a nutrient mixture in Y-79 malignant retinoblastoma cells
title_full_unstemmed Antineoplastic activity of a nutrient mixture in Y-79 malignant retinoblastoma cells
title_short Antineoplastic activity of a nutrient mixture in Y-79 malignant retinoblastoma cells
title_sort antineoplastic activity of a nutrient mixture in y-79 malignant retinoblastoma cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583477/
https://www.ncbi.nlm.nih.gov/pubmed/23129147
http://dx.doi.org/10.3892/or.2012.2110
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