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ADAM 12: A Putative Marker of Oligodendrogliomas?

ADAM 12 (meltrin alpha) belongs to a large family of molecules, consisting of members with both disintegrin and metalloproteinase properties. ADAMs have been implicated in several cell physiological processes including cell adhesion, cell fusion, proteolysis and signalling. ADAM 12 is widely express...

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Autores principales: Kanakis, Dimitrios, Lendeckel, Uwe, Theodosiou, Paraskevi, Dobrowolny, Henrik, Mawrin, Christian, Keilhoff, Gerburg, Bukowska, Alicia, Dietzmann, Knut, Bogerts, Bernhard, Bernstein, Hans-Gert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810230/
https://www.ncbi.nlm.nih.gov/pubmed/23324579
http://dx.doi.org/10.3233/DMA-120953
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author Kanakis, Dimitrios
Lendeckel, Uwe
Theodosiou, Paraskevi
Dobrowolny, Henrik
Mawrin, Christian
Keilhoff, Gerburg
Bukowska, Alicia
Dietzmann, Knut
Bogerts, Bernhard
Bernstein, Hans-Gert
author_facet Kanakis, Dimitrios
Lendeckel, Uwe
Theodosiou, Paraskevi
Dobrowolny, Henrik
Mawrin, Christian
Keilhoff, Gerburg
Bukowska, Alicia
Dietzmann, Knut
Bogerts, Bernhard
Bernstein, Hans-Gert
author_sort Kanakis, Dimitrios
collection PubMed
description ADAM 12 (meltrin alpha) belongs to a large family of molecules, consisting of members with both disintegrin and metalloproteinase properties. ADAMs have been implicated in several cell physiological processes including cell adhesion, cell fusion, proteolysis and signalling. ADAM 12 is widely expressed, including skeletal muscle, testis, bone, intestine, heart and kidney. In addition, a variety of tumours show elevated expression of ADAM12; among them being breast-, colon-, gastric- and lung-carcinoma. As to the brain, ADAM 12 has been shown previously to be expressed in rat and human oligodendrocytes. However, little is known about the expression of this protease in brain tumours. This study demonstrates the presence of ADAM 12 in non-neoplastic oligodendroglial cells of normal human brain as well as in neoplastic oligodendroglia and minigemistocytes arising from four pure oligodendrogliomas and three mixed oligoastrocytomas. Double stainings revealed a notable preference of ADAM 12 for the oligodendroglial over astroglial components. The results of immunohistochemistry are in accordance with the results obtained from the RT-PCR, which further demonstrated a mild difference concerning the mRNA concentration of ADAM 12 between similar grades of eight astrocytomas and eight oligodendrogliomas (namely four astrocytomas grade II versus four oligodendrogliomas grade II and four astrocytomas grade III versus four oligodendrogliomas grade III). Both cellular immunostaining for ADAM 12 and ADAM 12 mRNA content decrease with higher histologic grade of the tumour. Surprisingly, the latter parameter (ADAM12 mRNA) showed a significant opposite correlation to the degree of histologic tumour malignancy. From our data showing that ADAM 12 is highly expressed in, but not restricted to, oligodendrogliomas, we conclude that ADAM 12 immunohistochemistry may be a helpful tool in the diagnosis of brain tumours.
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spelling pubmed-38102302013-12-02 ADAM 12: A Putative Marker of Oligodendrogliomas? Kanakis, Dimitrios Lendeckel, Uwe Theodosiou, Paraskevi Dobrowolny, Henrik Mawrin, Christian Keilhoff, Gerburg Bukowska, Alicia Dietzmann, Knut Bogerts, Bernhard Bernstein, Hans-Gert Dis Markers Other ADAM 12 (meltrin alpha) belongs to a large family of molecules, consisting of members with both disintegrin and metalloproteinase properties. ADAMs have been implicated in several cell physiological processes including cell adhesion, cell fusion, proteolysis and signalling. ADAM 12 is widely expressed, including skeletal muscle, testis, bone, intestine, heart and kidney. In addition, a variety of tumours show elevated expression of ADAM12; among them being breast-, colon-, gastric- and lung-carcinoma. As to the brain, ADAM 12 has been shown previously to be expressed in rat and human oligodendrocytes. However, little is known about the expression of this protease in brain tumours. This study demonstrates the presence of ADAM 12 in non-neoplastic oligodendroglial cells of normal human brain as well as in neoplastic oligodendroglia and minigemistocytes arising from four pure oligodendrogliomas and three mixed oligoastrocytomas. Double stainings revealed a notable preference of ADAM 12 for the oligodendroglial over astroglial components. The results of immunohistochemistry are in accordance with the results obtained from the RT-PCR, which further demonstrated a mild difference concerning the mRNA concentration of ADAM 12 between similar grades of eight astrocytomas and eight oligodendrogliomas (namely four astrocytomas grade II versus four oligodendrogliomas grade II and four astrocytomas grade III versus four oligodendrogliomas grade III). Both cellular immunostaining for ADAM 12 and ADAM 12 mRNA content decrease with higher histologic grade of the tumour. Surprisingly, the latter parameter (ADAM12 mRNA) showed a significant opposite correlation to the degree of histologic tumour malignancy. From our data showing that ADAM 12 is highly expressed in, but not restricted to, oligodendrogliomas, we conclude that ADAM 12 immunohistochemistry may be a helpful tool in the diagnosis of brain tumours. IOS Press 2013 2013-01-24 /pmc/articles/PMC3810230/ /pubmed/23324579 http://dx.doi.org/10.3233/DMA-120953 Text en Copyright © 2013 Hindawi Publishing Corporation.
spellingShingle Other
Kanakis, Dimitrios
Lendeckel, Uwe
Theodosiou, Paraskevi
Dobrowolny, Henrik
Mawrin, Christian
Keilhoff, Gerburg
Bukowska, Alicia
Dietzmann, Knut
Bogerts, Bernhard
Bernstein, Hans-Gert
ADAM 12: A Putative Marker of Oligodendrogliomas?
title ADAM 12: A Putative Marker of Oligodendrogliomas?
title_full ADAM 12: A Putative Marker of Oligodendrogliomas?
title_fullStr ADAM 12: A Putative Marker of Oligodendrogliomas?
title_full_unstemmed ADAM 12: A Putative Marker of Oligodendrogliomas?
title_short ADAM 12: A Putative Marker of Oligodendrogliomas?
title_sort adam 12: a putative marker of oligodendrogliomas?
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810230/
https://www.ncbi.nlm.nih.gov/pubmed/23324579
http://dx.doi.org/10.3233/DMA-120953
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