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N-myristoyltransferase: A potential novel diagnostic marker for colon cancer

BACKGROUND: Colon cancer is the second leading cause of cancer deaths in the western world. If detected early, colorectal cancer is one of the most treatable forms of cancer. Unfortunately, very few people are screened. N-myristoyltransferase (NMT) catalyzes myristoylation of various proteins includ...

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Autores principales: Shrivastav, Anuraag, Varma, Shailly, Saxena, Anurag, DeCoteau, John, Sharma, Rajendra K
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2203986/
https://www.ncbi.nlm.nih.gov/pubmed/18021392
http://dx.doi.org/10.1186/1479-5876-5-58
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author Shrivastav, Anuraag
Varma, Shailly
Saxena, Anurag
DeCoteau, John
Sharma, Rajendra K
author_facet Shrivastav, Anuraag
Varma, Shailly
Saxena, Anurag
DeCoteau, John
Sharma, Rajendra K
author_sort Shrivastav, Anuraag
collection PubMed
description BACKGROUND: Colon cancer is the second leading cause of cancer deaths in the western world. If detected early, colorectal cancer is one of the most treatable forms of cancer. Unfortunately, very few people are screened. N-myristoyltransferase (NMT) catalyzes myristoylation of various proteins including oncoproteins. We have demonstrated earlier the alteration of NMT activity during the progression of colorectal cancer and established NMT as a putative therapeutic target for cancer. METHODS: Peripheral blood samples and bone marrow were collected from the colon cancer patients and azoxymethane induced colonic tumor rats and their controls respectively. NMT activity and expression was determined as reported earlier. Immunohistochemical studies were carried out using standard procedures. RESULTS: In this study we demonstrate for the first time altered expression and localization of NMT in the peripheral blood and bone marrow in colon cancer patients. Immunohistochemical analysis revealed weak to negative staining for NMT in peripheral blood mononuclear cells (PBMC) of controls, whereas strong positivity was observed in PBMC colon cancer patients. In addition, we observed that NMT was localized mostly in the nuclei of the bone marrow (BM) mononuclear cells of the colon cancer patients, whereas NMT remained cytoplasmic in the control bone marrow specimens. CONCLUSION: The strikingly different NMT expression offers the basis of a potential adjunct investigative tool for screening or diagnosis of patients at risk for or suspected of having colon cancer. Furthermore, altered localization of NMT in BM of tumor bearing hosts may serve as an added investigative tool for the diagnostic purpose.
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spelling pubmed-22039862008-01-17 N-myristoyltransferase: A potential novel diagnostic marker for colon cancer Shrivastav, Anuraag Varma, Shailly Saxena, Anurag DeCoteau, John Sharma, Rajendra K J Transl Med Research BACKGROUND: Colon cancer is the second leading cause of cancer deaths in the western world. If detected early, colorectal cancer is one of the most treatable forms of cancer. Unfortunately, very few people are screened. N-myristoyltransferase (NMT) catalyzes myristoylation of various proteins including oncoproteins. We have demonstrated earlier the alteration of NMT activity during the progression of colorectal cancer and established NMT as a putative therapeutic target for cancer. METHODS: Peripheral blood samples and bone marrow were collected from the colon cancer patients and azoxymethane induced colonic tumor rats and their controls respectively. NMT activity and expression was determined as reported earlier. Immunohistochemical studies were carried out using standard procedures. RESULTS: In this study we demonstrate for the first time altered expression and localization of NMT in the peripheral blood and bone marrow in colon cancer patients. Immunohistochemical analysis revealed weak to negative staining for NMT in peripheral blood mononuclear cells (PBMC) of controls, whereas strong positivity was observed in PBMC colon cancer patients. In addition, we observed that NMT was localized mostly in the nuclei of the bone marrow (BM) mononuclear cells of the colon cancer patients, whereas NMT remained cytoplasmic in the control bone marrow specimens. CONCLUSION: The strikingly different NMT expression offers the basis of a potential adjunct investigative tool for screening or diagnosis of patients at risk for or suspected of having colon cancer. Furthermore, altered localization of NMT in BM of tumor bearing hosts may serve as an added investigative tool for the diagnostic purpose. BioMed Central 2007-11-16 /pmc/articles/PMC2203986/ /pubmed/18021392 http://dx.doi.org/10.1186/1479-5876-5-58 Text en Copyright © 2007 Shrivastav et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Shrivastav, Anuraag
Varma, Shailly
Saxena, Anurag
DeCoteau, John
Sharma, Rajendra K
N-myristoyltransferase: A potential novel diagnostic marker for colon cancer
title N-myristoyltransferase: A potential novel diagnostic marker for colon cancer
title_full N-myristoyltransferase: A potential novel diagnostic marker for colon cancer
title_fullStr N-myristoyltransferase: A potential novel diagnostic marker for colon cancer
title_full_unstemmed N-myristoyltransferase: A potential novel diagnostic marker for colon cancer
title_short N-myristoyltransferase: A potential novel diagnostic marker for colon cancer
title_sort n-myristoyltransferase: a potential novel diagnostic marker for colon cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2203986/
https://www.ncbi.nlm.nih.gov/pubmed/18021392
http://dx.doi.org/10.1186/1479-5876-5-58
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