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Fibrillin-1 (FBN-1) a new marker of germ cell neoplasia in situ

BACKGROUND: Germ cell neoplasia in situ (GCNIS), is preinvasive stage of testicular germ cell tumours (TGCTs). Fibrillins, which are integral components of microfibrils are suggested to be involved in cancer pathogenesis and maintenance of embryonic stem cells pluripotency. The aim of this study was...

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Autores principales: Cierna, Z., Mego, M., Jurisica, I., Machalekova, K., Chovanec, M., Miskovska, V., Svetlovska, D., Kalavska, K., Rejlekova, K., Kajo, K., Mardiak, J., Babal, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973050/
https://www.ncbi.nlm.nih.gov/pubmed/27487789
http://dx.doi.org/10.1186/s12885-016-2644-z
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author Cierna, Z.
Mego, M.
Jurisica, I.
Machalekova, K.
Chovanec, M.
Miskovska, V.
Svetlovska, D.
Kalavska, K.
Rejlekova, K.
Kajo, K.
Mardiak, J.
Babal, P.
author_facet Cierna, Z.
Mego, M.
Jurisica, I.
Machalekova, K.
Chovanec, M.
Miskovska, V.
Svetlovska, D.
Kalavska, K.
Rejlekova, K.
Kajo, K.
Mardiak, J.
Babal, P.
author_sort Cierna, Z.
collection PubMed
description BACKGROUND: Germ cell neoplasia in situ (GCNIS), is preinvasive stage of testicular germ cell tumours (TGCTs). Fibrillins, which are integral components of microfibrils are suggested to be involved in cancer pathogenesis and maintenance of embryonic stem cells pluripotency. The aim of this study was to examine fibrillin-1 (FBN-1) expression in TGCTs patients. METHODS: Surgical specimens from 203 patients with TGCTs were included into the translational study. FBN-1 expression was evaluated in the tumour tissue, in GCNIS and in adjacent non-neoplastic testicular tissue in all available cases. Tissue samples were processed by the tissue microarray method. FBN-1 was detected by immunohistochemistry using goat polyclonal antibody and the expression was evaluated by the multiplicative quickscore (QS). RESULTS: The highest FBN-1 positivity was detected in GCNIS (mean QS = 11.30), with overexpression of FBN-1 (QS >9) in the majority (77.1 %) of cases. Expression of FBN-1 in all subtypes of TGCTs was significantly lower in comparison to expression in GCNIS (all p <0.001). Seminoma had significantly higher expression compared to EC, ChC and TER (all p <0.05), but not to YST (p = 0.84). In non-neoplastic testicular tissue the FBN-1 positivity was very low (mean QS = 0.02). Sensitivity, specificity, positive and negative predictive value of FBN-1 expression for diagnosis of GCNIS were 97.1, 98.8, 98.6 and 97.7 %. CONCLUSIONS: FBN-1 is overexpressed in TGCTs and especially in GCNIS when compared to non-neoplastic testicular tissue in patients with germ cell tumors and could be involved in germ cell neoplasia in situ development.
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spelling pubmed-49730502016-08-05 Fibrillin-1 (FBN-1) a new marker of germ cell neoplasia in situ Cierna, Z. Mego, M. Jurisica, I. Machalekova, K. Chovanec, M. Miskovska, V. Svetlovska, D. Kalavska, K. Rejlekova, K. Kajo, K. Mardiak, J. Babal, P. BMC Cancer Research Article BACKGROUND: Germ cell neoplasia in situ (GCNIS), is preinvasive stage of testicular germ cell tumours (TGCTs). Fibrillins, which are integral components of microfibrils are suggested to be involved in cancer pathogenesis and maintenance of embryonic stem cells pluripotency. The aim of this study was to examine fibrillin-1 (FBN-1) expression in TGCTs patients. METHODS: Surgical specimens from 203 patients with TGCTs were included into the translational study. FBN-1 expression was evaluated in the tumour tissue, in GCNIS and in adjacent non-neoplastic testicular tissue in all available cases. Tissue samples were processed by the tissue microarray method. FBN-1 was detected by immunohistochemistry using goat polyclonal antibody and the expression was evaluated by the multiplicative quickscore (QS). RESULTS: The highest FBN-1 positivity was detected in GCNIS (mean QS = 11.30), with overexpression of FBN-1 (QS >9) in the majority (77.1 %) of cases. Expression of FBN-1 in all subtypes of TGCTs was significantly lower in comparison to expression in GCNIS (all p <0.001). Seminoma had significantly higher expression compared to EC, ChC and TER (all p <0.05), but not to YST (p = 0.84). In non-neoplastic testicular tissue the FBN-1 positivity was very low (mean QS = 0.02). Sensitivity, specificity, positive and negative predictive value of FBN-1 expression for diagnosis of GCNIS were 97.1, 98.8, 98.6 and 97.7 %. CONCLUSIONS: FBN-1 is overexpressed in TGCTs and especially in GCNIS when compared to non-neoplastic testicular tissue in patients with germ cell tumors and could be involved in germ cell neoplasia in situ development. BioMed Central 2016-08-04 /pmc/articles/PMC4973050/ /pubmed/27487789 http://dx.doi.org/10.1186/s12885-016-2644-z Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Cierna, Z.
Mego, M.
Jurisica, I.
Machalekova, K.
Chovanec, M.
Miskovska, V.
Svetlovska, D.
Kalavska, K.
Rejlekova, K.
Kajo, K.
Mardiak, J.
Babal, P.
Fibrillin-1 (FBN-1) a new marker of germ cell neoplasia in situ
title Fibrillin-1 (FBN-1) a new marker of germ cell neoplasia in situ
title_full Fibrillin-1 (FBN-1) a new marker of germ cell neoplasia in situ
title_fullStr Fibrillin-1 (FBN-1) a new marker of germ cell neoplasia in situ
title_full_unstemmed Fibrillin-1 (FBN-1) a new marker of germ cell neoplasia in situ
title_short Fibrillin-1 (FBN-1) a new marker of germ cell neoplasia in situ
title_sort fibrillin-1 (fbn-1) a new marker of germ cell neoplasia in situ
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973050/
https://www.ncbi.nlm.nih.gov/pubmed/27487789
http://dx.doi.org/10.1186/s12885-016-2644-z
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