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Over-Expression of Cyclooxygenase-2 in Colorectal Cancer Patients

BACKGROUND: Colorectal carcinoma (CRC) is the most common neoplasm of the gastrointestinal tract. COX-2 plays an important role in CRC development and is a key target for the regression of colorectal tumorigenesis by non-steroidal anti-inflammatory drugs. The present study was conducted to examine t...

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Autores principales: Negi, Ram Rattan, Rana, Satya Vati, Gupta, Vikas, Gupta, Rajesh, Chadha, Vijayta Dani, Prasad, Kaushal Kishor, Dhawan, Devinder K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021602/
https://www.ncbi.nlm.nih.gov/pubmed/31244287
http://dx.doi.org/10.31557/APJCP.2019.20.6.1675
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author Negi, Ram Rattan
Rana, Satya Vati
Gupta, Vikas
Gupta, Rajesh
Chadha, Vijayta Dani
Prasad, Kaushal Kishor
Dhawan, Devinder K
author_facet Negi, Ram Rattan
Rana, Satya Vati
Gupta, Vikas
Gupta, Rajesh
Chadha, Vijayta Dani
Prasad, Kaushal Kishor
Dhawan, Devinder K
author_sort Negi, Ram Rattan
collection PubMed
description BACKGROUND: Colorectal carcinoma (CRC) is the most common neoplasm of the gastrointestinal tract. COX-2 plays an important role in CRC development and is a key target for the regression of colorectal tumorigenesis by non-steroidal anti-inflammatory drugs. The present study was conducted to examine the relationship of the levels of COX-2 in CRC patients with the clinico-pathological parameters and also to assess its usefulness as a potential biomarker for diagnosis of CRC. METHODS: Prior to surgery, 30 CRC patients were enrolled and the samples from colon tumors and surrounding tissues were taken after they underwent surgical intervention at PGIMER, Chandigarh. mRNA expression levels of COX-2 were examined in 30 CRC and adjacent normal colonic mucosa by quantitative polymerase chain reaction (qPCR). The expression of COX-2 was assessed by immunohistochemical method using rabbit polyclonal antibodies against human COX-2 protein. RESULTS: The quantitative relative expression of COX-2 mRNA was observed to be significantly higher (p<0.05) in colorectal cancer tissues as compared to adjacent normal colon tissues. Also, female CRC patients showed significantly higher (p<0.009) expression of COX-2 mRNA vis-a-vis male colorectal cancer patients. This is the first study which has reported a direct relationship between COX-2 mRNA expressions in male colorectal cancer patients versus females. Further, immunohistochemistry of COX-2 confirmed the quantitative real time-PCR findings. CONCLUSION: Our study shows that COX-2 over expression in colorectal carcinoma patients is closely associated with clinico-pathological parameters and is more pronounced in males versus females. Further, COX-2 mRNA expression can serve as a potential biomarker for the diagnosis of CRC.
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spelling pubmed-70216022020-02-25 Over-Expression of Cyclooxygenase-2 in Colorectal Cancer Patients Negi, Ram Rattan Rana, Satya Vati Gupta, Vikas Gupta, Rajesh Chadha, Vijayta Dani Prasad, Kaushal Kishor Dhawan, Devinder K Asian Pac J Cancer Prev Research Article BACKGROUND: Colorectal carcinoma (CRC) is the most common neoplasm of the gastrointestinal tract. COX-2 plays an important role in CRC development and is a key target for the regression of colorectal tumorigenesis by non-steroidal anti-inflammatory drugs. The present study was conducted to examine the relationship of the levels of COX-2 in CRC patients with the clinico-pathological parameters and also to assess its usefulness as a potential biomarker for diagnosis of CRC. METHODS: Prior to surgery, 30 CRC patients were enrolled and the samples from colon tumors and surrounding tissues were taken after they underwent surgical intervention at PGIMER, Chandigarh. mRNA expression levels of COX-2 were examined in 30 CRC and adjacent normal colonic mucosa by quantitative polymerase chain reaction (qPCR). The expression of COX-2 was assessed by immunohistochemical method using rabbit polyclonal antibodies against human COX-2 protein. RESULTS: The quantitative relative expression of COX-2 mRNA was observed to be significantly higher (p<0.05) in colorectal cancer tissues as compared to adjacent normal colon tissues. Also, female CRC patients showed significantly higher (p<0.009) expression of COX-2 mRNA vis-a-vis male colorectal cancer patients. This is the first study which has reported a direct relationship between COX-2 mRNA expressions in male colorectal cancer patients versus females. Further, immunohistochemistry of COX-2 confirmed the quantitative real time-PCR findings. CONCLUSION: Our study shows that COX-2 over expression in colorectal carcinoma patients is closely associated with clinico-pathological parameters and is more pronounced in males versus females. Further, COX-2 mRNA expression can serve as a potential biomarker for the diagnosis of CRC. West Asia Organization for Cancer Prevention 2019 /pmc/articles/PMC7021602/ /pubmed/31244287 http://dx.doi.org/10.31557/APJCP.2019.20.6.1675 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
Negi, Ram Rattan
Rana, Satya Vati
Gupta, Vikas
Gupta, Rajesh
Chadha, Vijayta Dani
Prasad, Kaushal Kishor
Dhawan, Devinder K
Over-Expression of Cyclooxygenase-2 in Colorectal Cancer Patients
title Over-Expression of Cyclooxygenase-2 in Colorectal Cancer Patients
title_full Over-Expression of Cyclooxygenase-2 in Colorectal Cancer Patients
title_fullStr Over-Expression of Cyclooxygenase-2 in Colorectal Cancer Patients
title_full_unstemmed Over-Expression of Cyclooxygenase-2 in Colorectal Cancer Patients
title_short Over-Expression of Cyclooxygenase-2 in Colorectal Cancer Patients
title_sort over-expression of cyclooxygenase-2 in colorectal cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021602/
https://www.ncbi.nlm.nih.gov/pubmed/31244287
http://dx.doi.org/10.31557/APJCP.2019.20.6.1675
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