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TRAIL protein expression in breast cancer cells correlates with nuclear grade

INTRODUCTION: TRAIL protein may serve as an escape mechanism for cancer cells from the immune response. The aim of the study was to assess whether the presence of TRAIL protein correlates with unfavourable prognostic factors in breast carcinoma. MATERIAL AND METHODS: The study group was composed of...

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Autores principales: Bilski, Adam, Pasz-Walczak, Grażyna, Kubiak, Robert, Sek, Piotr, Chalubinska, Justyna, Fendler, Wojciech, Wronski, Konrad, Piekarska, Anna, Pluta, Piotr, Potemski, Piotr, Jeziorski, Arkadiusz, Piekarski, Janusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284069/
https://www.ncbi.nlm.nih.gov/pubmed/22371798
http://dx.doi.org/10.5114/aoms.2010.14466
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author Bilski, Adam
Pasz-Walczak, Grażyna
Kubiak, Robert
Sek, Piotr
Chalubinska, Justyna
Fendler, Wojciech
Wronski, Konrad
Piekarska, Anna
Pluta, Piotr
Potemski, Piotr
Jeziorski, Arkadiusz
Piekarski, Janusz
author_facet Bilski, Adam
Pasz-Walczak, Grażyna
Kubiak, Robert
Sek, Piotr
Chalubinska, Justyna
Fendler, Wojciech
Wronski, Konrad
Piekarska, Anna
Pluta, Piotr
Potemski, Piotr
Jeziorski, Arkadiusz
Piekarski, Janusz
author_sort Bilski, Adam
collection PubMed
description INTRODUCTION: TRAIL protein may serve as an escape mechanism for cancer cells from the immune response. The aim of the study was to assess whether the presence of TRAIL protein correlates with unfavourable prognostic factors in breast carcinoma. MATERIAL AND METHODS: The study group was composed of breast cancer patients treated surgically in the Department of Surgical Oncology, Medical University of Lodz, Poland, from January to December 2003. Inclusion criteria for the study were fulfilled by 117 women. The immunohistochemical study of TRAIL protein expression was performed in 118 breast carcinomas diagnosed in the study group. TRAIL protein expression was correlated with other variables: tumour size, lymph node status, grade, histological type of carcinoma, oestrogen and progesterone receptor status, HER2 expression, presence of lymphovascular invasion and age of the patient. RESULTS: Expression of TRAIL protein was present in 73% of breast carcinomas. The percentage of TRAIL-expressing breast carcinoma cells correlated with the nuclear grade (τ = 0.26, p < 0.05; Tau Kendall test). The intensity of TRAIL expression (intensity of staining) in breast carcinoma cells correlated with the nuclear grade (τ = 0.15, p < 0.05; Tau Kendall test). TRAIL expression in breast carcinoma did not correlate with other studied variables. CONCLUSIONS: Our analysis revealed that expression of TRAIL protein in breast carcinoma cells correlates with nuclear grade of carcinoma.
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spelling pubmed-32840692012-02-27 TRAIL protein expression in breast cancer cells correlates with nuclear grade Bilski, Adam Pasz-Walczak, Grażyna Kubiak, Robert Sek, Piotr Chalubinska, Justyna Fendler, Wojciech Wronski, Konrad Piekarska, Anna Pluta, Piotr Potemski, Piotr Jeziorski, Arkadiusz Piekarski, Janusz Arch Med Sci Clinical Research INTRODUCTION: TRAIL protein may serve as an escape mechanism for cancer cells from the immune response. The aim of the study was to assess whether the presence of TRAIL protein correlates with unfavourable prognostic factors in breast carcinoma. MATERIAL AND METHODS: The study group was composed of breast cancer patients treated surgically in the Department of Surgical Oncology, Medical University of Lodz, Poland, from January to December 2003. Inclusion criteria for the study were fulfilled by 117 women. The immunohistochemical study of TRAIL protein expression was performed in 118 breast carcinomas diagnosed in the study group. TRAIL protein expression was correlated with other variables: tumour size, lymph node status, grade, histological type of carcinoma, oestrogen and progesterone receptor status, HER2 expression, presence of lymphovascular invasion and age of the patient. RESULTS: Expression of TRAIL protein was present in 73% of breast carcinomas. The percentage of TRAIL-expressing breast carcinoma cells correlated with the nuclear grade (τ = 0.26, p < 0.05; Tau Kendall test). The intensity of TRAIL expression (intensity of staining) in breast carcinoma cells correlated with the nuclear grade (τ = 0.15, p < 0.05; Tau Kendall test). TRAIL expression in breast carcinoma did not correlate with other studied variables. CONCLUSIONS: Our analysis revealed that expression of TRAIL protein in breast carcinoma cells correlates with nuclear grade of carcinoma. Termedia Publishing House 2010-09-07 2010-08-30 /pmc/articles/PMC3284069/ /pubmed/22371798 http://dx.doi.org/10.5114/aoms.2010.14466 Text en Copyright © 2010 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research
Bilski, Adam
Pasz-Walczak, Grażyna
Kubiak, Robert
Sek, Piotr
Chalubinska, Justyna
Fendler, Wojciech
Wronski, Konrad
Piekarska, Anna
Pluta, Piotr
Potemski, Piotr
Jeziorski, Arkadiusz
Piekarski, Janusz
TRAIL protein expression in breast cancer cells correlates with nuclear grade
title TRAIL protein expression in breast cancer cells correlates with nuclear grade
title_full TRAIL protein expression in breast cancer cells correlates with nuclear grade
title_fullStr TRAIL protein expression in breast cancer cells correlates with nuclear grade
title_full_unstemmed TRAIL protein expression in breast cancer cells correlates with nuclear grade
title_short TRAIL protein expression in breast cancer cells correlates with nuclear grade
title_sort trail protein expression in breast cancer cells correlates with nuclear grade
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284069/
https://www.ncbi.nlm.nih.gov/pubmed/22371798
http://dx.doi.org/10.5114/aoms.2010.14466
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