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Original Article
129 (
1
); 89-94
doi:
10.25259/IJMR_20091291_89

Expression of class III β-tubulin in colorectal carcinomas: an immunohistochemical study using TU-20 & TuJ-1 antibody

Department of Pathology, 3rd Faculty of Medicine, Charles University, Prague, Czech Republic
Department of Radiotherapy & Oncology, 3rd Faculty of Medicine, Charles University, Prague, Czech Republic

Reprint requests: Dr Tomáš Jirásek, Department of Pathology, 3rd Faculty of Medicine, Šrobárova 50, 10034 Prague, Czech Republic e-mail: tjirasek@fnkv.cz

Licence
This open access article is licensed under Creative Commons Attribution 4.0 International (CC BY 4.0). http://creativecommons.org/licenses/by/4.0

Abstract

Background & objectives:

Expression of class III β-tubulin represents newly discovered marker of resistance to taxol-based chemotherapy in a wide spectra of carcinomas. However, very little is known about its expression in colorectal carcinomas. This study was done to determine class III β-tubulin expression in a large series of colonic carcinomas, covering tumours with different degree of differentiation in order to evaluate its prospective significance in resistance to taxol-based chemotherapeutics and to compare the immunostaining profile of two widely used monoclonal antibodies, TU-20 and TuJ-1.

Methods:

Sixty patients with colorectal carcinoma were enrolled; all of them were treated surgically by the resection. Twenty tumours were histologically assessed as G1, 20 as G2 and 20 as G3. Routine immunohistochemical procedure using TU-20 and TuJ-1 mouse monoclonal antibodies was applied to all 60 specimen and slides were evaluated using an optical microscope.

Results:

Expression of class III β-tubulin was detected in 14 tumours (23.3%), while remaining tumours were negative. Relatively higher frequency of class III β-tubulin expression was observed in G3 tumours (10 cases) in comparison with G1 (3 cases) and G2 (1 case), respectively. Seven tumours displayed positive immunostaining with both tested antibodies TU-20 and TuJ-1. Six tumours showed expression of class III β- tubulin in more than 1 per cent of neoplastic cell population. In remaining 8 tumours only individual scattered neoplastic cells exhibited class III β-tubulin expression either with TU-20, or with TuJ-1 antibody.

Interpretation & conclusion:

Higher frequency of immunoreactivity was observed in poorly differentiated tumours. However, more than 90 per cent of neoplastic cell population did not express class III β-tubulin in almost all tumours. These negative cells of colonic cancer could represent the potential target for taxane-based chemotherapy in the future. Our results indicate that TU-20 and TuJ-1 antibodies exhibit very similar immunoreactivity in neoplastic tissue.

Keywords

Class III β-tubulin
colorectal cancer

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