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Liver Pathology in Rats Treated with Newcastle Disease Virus Strains AF2240 and V4-UPM
BACKGROUND: Treatment of cancer with chemo-radiotherapy causes severe side effects due to cytotoxic effects towards normal tissues which often results in morbidity. Therefore, developing anticancer agents which can selectively target the cancer cells and cause less side effects are the main objectiv...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
West Asia Organization for Cancer Prevention
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982671/ https://www.ncbi.nlm.nih.gov/pubmed/31653156 http://dx.doi.org/10.31557/APJCP.2019.20.10.3071 |
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author | Assayaghi, Rowa Mohammed Alabsi, Aied Mohammed Swethadri, Gumballi Ali, Abdul Manaf |
author_facet | Assayaghi, Rowa Mohammed Alabsi, Aied Mohammed Swethadri, Gumballi Ali, Abdul Manaf |
author_sort | Assayaghi, Rowa Mohammed |
collection | PubMed |
description | BACKGROUND: Treatment of cancer with chemo-radiotherapy causes severe side effects due to cytotoxic effects towards normal tissues which often results in morbidity. Therefore, developing anticancer agents which can selectively target the cancer cells and cause less side effects are the main objectives of the new therapeutic strategies for treatment advanced or metastatic cancers. Newcastle disease virus strains AF2240 and V4-UPM were shown to be cytolytic against various cancer cells in-vitro and very effective as antileukemicagents. METHODS: 45 rats at 6 weeks of age, were randomly assigned to nine groups with 5 rats in each group, both azoxymethane (AOM) and 5-Fluorouracil (5-FU) were given to rats according to the body weight. NDV virus strains (AF2240 and V4-UPM) doses were determined to rats according to CD50 resulted from MTT assay. After 8 doses of NDV strians and 5-FU, tissue sections preparations and histopathological study of rats’ organs were done. RESULTS: In this article morphological changes of rats’ organs, especially in livers, after treatment with a colon carcinogen (azoxymethane) and Newcastle disease virus strains have been recorded. We observed liver damage caused by AOM evidenced by morphological changes and enzymatic elevation were protected by the oncolytic viruses sections. Also we found that combination treatment NDV with 5-FU had greater antitumor efficacy than treatment with NDV or 5-FU alone. CONCLUSION: We noted morphological changes in liver and other rats’ organs due to a chemical carcinogen and their protection by NDV AF2240 and NDV V4-UPM seems to be most protective. |
format | Online Article Text |
id | pubmed-6982671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | West Asia Organization for Cancer Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-69826712020-07-07 Liver Pathology in Rats Treated with Newcastle Disease Virus Strains AF2240 and V4-UPM Assayaghi, Rowa Mohammed Alabsi, Aied Mohammed Swethadri, Gumballi Ali, Abdul Manaf Asian Pac J Cancer Prev Research Article BACKGROUND: Treatment of cancer with chemo-radiotherapy causes severe side effects due to cytotoxic effects towards normal tissues which often results in morbidity. Therefore, developing anticancer agents which can selectively target the cancer cells and cause less side effects are the main objectives of the new therapeutic strategies for treatment advanced or metastatic cancers. Newcastle disease virus strains AF2240 and V4-UPM were shown to be cytolytic against various cancer cells in-vitro and very effective as antileukemicagents. METHODS: 45 rats at 6 weeks of age, were randomly assigned to nine groups with 5 rats in each group, both azoxymethane (AOM) and 5-Fluorouracil (5-FU) were given to rats according to the body weight. NDV virus strains (AF2240 and V4-UPM) doses were determined to rats according to CD50 resulted from MTT assay. After 8 doses of NDV strians and 5-FU, tissue sections preparations and histopathological study of rats’ organs were done. RESULTS: In this article morphological changes of rats’ organs, especially in livers, after treatment with a colon carcinogen (azoxymethane) and Newcastle disease virus strains have been recorded. We observed liver damage caused by AOM evidenced by morphological changes and enzymatic elevation were protected by the oncolytic viruses sections. Also we found that combination treatment NDV with 5-FU had greater antitumor efficacy than treatment with NDV or 5-FU alone. CONCLUSION: We noted morphological changes in liver and other rats’ organs due to a chemical carcinogen and their protection by NDV AF2240 and NDV V4-UPM seems to be most protective. West Asia Organization for Cancer Prevention 2019 /pmc/articles/PMC6982671/ /pubmed/31653156 http://dx.doi.org/10.31557/APJCP.2019.20.10.3071 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Assayaghi, Rowa Mohammed Alabsi, Aied Mohammed Swethadri, Gumballi Ali, Abdul Manaf Liver Pathology in Rats Treated with Newcastle Disease Virus Strains AF2240 and V4-UPM |
title | Liver Pathology in Rats Treated with Newcastle Disease Virus Strains AF2240 and V4-UPM |
title_full | Liver Pathology in Rats Treated with Newcastle Disease Virus Strains AF2240 and V4-UPM |
title_fullStr | Liver Pathology in Rats Treated with Newcastle Disease Virus Strains AF2240 and V4-UPM |
title_full_unstemmed | Liver Pathology in Rats Treated with Newcastle Disease Virus Strains AF2240 and V4-UPM |
title_short | Liver Pathology in Rats Treated with Newcastle Disease Virus Strains AF2240 and V4-UPM |
title_sort | liver pathology in rats treated with newcastle disease virus strains af2240 and v4-upm |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982671/ https://www.ncbi.nlm.nih.gov/pubmed/31653156 http://dx.doi.org/10.31557/APJCP.2019.20.10.3071 |
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