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Expression of Septin 2 and Her2/neu in Colorectal Cancer

BACKGROUND: Colorectal cancer (CRC) is a common and lethal disease. Septin 2 belongs to the same class of GTPases as the RAS oncogenes influence the invasion and metastasis of many types of tumor cells. Furthermore, HER2/neu is involved in the tumor genesis and progression of various types of tumors...

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Autores principales: Hanbuli, Hala M. El, Amer, Samar Ibrahim Ismail, Ibrahim, Heba A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846928/
https://www.ncbi.nlm.nih.gov/pubmed/36687331
http://dx.doi.org/10.4103/jmau.jmau_38_21
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author Hanbuli, Hala M. El
Amer, Samar Ibrahim Ismail
Ibrahim, Heba A.
author_facet Hanbuli, Hala M. El
Amer, Samar Ibrahim Ismail
Ibrahim, Heba A.
author_sort Hanbuli, Hala M. El
collection PubMed
description BACKGROUND: Colorectal cancer (CRC) is a common and lethal disease. Septin 2 belongs to the same class of GTPases as the RAS oncogenes influence the invasion and metastasis of many types of tumor cells. Furthermore, HER2/neu is involved in the tumor genesis and progression of various types of tumors. The role of both molecules is still questionable in CRC. AIM: The aim of the study is to examine the expression of septin 2 and Her2/neu in patients with CRC. MATERIALS AND METHODS: The study was conducted on 2 groups; the first group consisted of 70 paraffin blocks for CRC patients and the second group was formed of 24 blocks from patients diagnosed as colorectal adenoma. For each adenoma and carcinoma case, a section was immunohistochemically stained using antihuman SEPT2 polyclonal antibody. For each carcinoma case, another section was immunostained using monoclonal anti-HER2/neu. The results were statistically analyzed and compared with the collected clinicopathologic data of the cases. RESULTS: For the carcinoma patients, there was a significant association between SEPT2 staining intensity and histologic type (P = 0.001) and grade (P < 0.001), tumor T (P = 0.001) and N (P = 0.011) stages and the presence of lymphovascular invasion (P < 0.001) and a significant association between Her2/neu immunoreactivity scores (IRSs) and histologic grade (P = 0.048), tumor T (P < 0.001) and N (P = 0.019) stages and the presence of perineural (P = 0.004) and lymphovascular (P = 0.003) invasion. In colonic adenoma patients, there was a significant relation between septin 2 IRSs and the grade of dysplasia in the adenoma (P < 0.001) and significant relation with its expression in carcinoma group (P < 0.001). CONCLUSION: A potential prognostic role of septin 2 and Her2/neu for patients with CRC is suggested as expression of both markers was associated with many important prognostic clinicopathologic variables in patients of CRC.
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spelling pubmed-98469282023-01-19 Expression of Septin 2 and Her2/neu in Colorectal Cancer Hanbuli, Hala M. El Amer, Samar Ibrahim Ismail Ibrahim, Heba A. J Microsc Ultrastruct Original Article BACKGROUND: Colorectal cancer (CRC) is a common and lethal disease. Septin 2 belongs to the same class of GTPases as the RAS oncogenes influence the invasion and metastasis of many types of tumor cells. Furthermore, HER2/neu is involved in the tumor genesis and progression of various types of tumors. The role of both molecules is still questionable in CRC. AIM: The aim of the study is to examine the expression of septin 2 and Her2/neu in patients with CRC. MATERIALS AND METHODS: The study was conducted on 2 groups; the first group consisted of 70 paraffin blocks for CRC patients and the second group was formed of 24 blocks from patients diagnosed as colorectal adenoma. For each adenoma and carcinoma case, a section was immunohistochemically stained using antihuman SEPT2 polyclonal antibody. For each carcinoma case, another section was immunostained using monoclonal anti-HER2/neu. The results were statistically analyzed and compared with the collected clinicopathologic data of the cases. RESULTS: For the carcinoma patients, there was a significant association between SEPT2 staining intensity and histologic type (P = 0.001) and grade (P < 0.001), tumor T (P = 0.001) and N (P = 0.011) stages and the presence of lymphovascular invasion (P < 0.001) and a significant association between Her2/neu immunoreactivity scores (IRSs) and histologic grade (P = 0.048), tumor T (P < 0.001) and N (P = 0.019) stages and the presence of perineural (P = 0.004) and lymphovascular (P = 0.003) invasion. In colonic adenoma patients, there was a significant relation between septin 2 IRSs and the grade of dysplasia in the adenoma (P < 0.001) and significant relation with its expression in carcinoma group (P < 0.001). CONCLUSION: A potential prognostic role of septin 2 and Her2/neu for patients with CRC is suggested as expression of both markers was associated with many important prognostic clinicopathologic variables in patients of CRC. Wolters Kluwer - Medknow 2021-11-22 /pmc/articles/PMC9846928/ /pubmed/36687331 http://dx.doi.org/10.4103/jmau.jmau_38_21 Text en Copyright: © 2021 Journal of Microscopy and Ultrastructure https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Hanbuli, Hala M. El
Amer, Samar Ibrahim Ismail
Ibrahim, Heba A.
Expression of Septin 2 and Her2/neu in Colorectal Cancer
title Expression of Septin 2 and Her2/neu in Colorectal Cancer
title_full Expression of Septin 2 and Her2/neu in Colorectal Cancer
title_fullStr Expression of Septin 2 and Her2/neu in Colorectal Cancer
title_full_unstemmed Expression of Septin 2 and Her2/neu in Colorectal Cancer
title_short Expression of Septin 2 and Her2/neu in Colorectal Cancer
title_sort expression of septin 2 and her2/neu in colorectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846928/
https://www.ncbi.nlm.nih.gov/pubmed/36687331
http://dx.doi.org/10.4103/jmau.jmau_38_21
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