open access

Vol 68, No 4 (2017)
Original paper
Submitted: 2016-04-20
Accepted: 2016-10-13
Published online: 2017-05-26
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The “game” of glial fibrillary acidic and S100 proteins in pituitary adenomas: two players or several?

Anca Maria Cimpean1, Amalia Raluca Ceausu2, Ana Corlan3, Eugen Melnic4, Andreea Adriana Jitariu2, Marius Raica2
·
Pubmed: 28660986
·
Endokrynol Pol 2017;68(4):380-389.
Affiliations
  1. Department of Microscopic Morphology/Histology, Angiogenesis Research Centre, “Victor Babes” University of Medicine and Pharmacy Timişoara, Romania, Romania
  2. Department of Microscopic Morphology/Histology, Angiogenesis Research Centre, “Victor Babes” University of Medicine and Pharmacy Timişoara, Romania
  3. Department of Endocrinology, VAsile Goldis University, Arad, Romania, Romania
  4. Department of Pathology, Nicolae Testemitanu University of Medicine and Pharmacy Chisinau, Moldova, Moldova, Republic Of

open access

Vol 68, No 4 (2017)
Original Paper
Submitted: 2016-04-20
Accepted: 2016-10-13
Published online: 2017-05-26

Abstract

Introduction: S100 protein and GFAP expression in pituitary adenomas tumour cells is not well known; few correlations with other prognostic or therapeutic factors have previously been reported in pituitary adenomas. We aim to elucidate their involvement in the pathogenesis of pituitary adenomas and to establish the correlation of their expression with different growth factors and growth factor receptors known to have a prognostic and/or therapeutic role.

Material and methods: Sixty-one cases of pituitary adenomas were immunohistochemically assessed for the expression of GFAP and S100 protein in both tumour cells and FS cells, in close relationship with hormone profile, and correlated with vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR) expression, previously studied by our team.

Results: GFAP and S100 protein were expressed both in tumour cells and FS cells. Differences between morphology, distribution, and density of GFAP+ FS cells and S100+ FS cells were observed according to the hormone profile of pituitary adenomas. GFAP and S100 protein expression in tumour cells was significantly related to hormone profile of pituitary adenomas and also with VEGF and EGFR expression.

Conclusions: GFAP and S100 protein expressions in tumour cells from pituitary adenomas are influenced by hormone profile. Our re­sults support the presence of two molecular subtypes of FS cells GFAP+/VEGF+/S100 respectively and another one that is GFAP-/S100+/EGFR+ simultaneously with the classical variant GFAP+/S100+. It is possible that S100+/EGFR+ pituitary adenomas represent a group of pituitary adenomas with an aggressive behaviour and a high ability of invasion and recurrence.

Abstract

Introduction: S100 protein and GFAP expression in pituitary adenomas tumour cells is not well known; few correlations with other prognostic or therapeutic factors have previously been reported in pituitary adenomas. We aim to elucidate their involvement in the pathogenesis of pituitary adenomas and to establish the correlation of their expression with different growth factors and growth factor receptors known to have a prognostic and/or therapeutic role.

Material and methods: Sixty-one cases of pituitary adenomas were immunohistochemically assessed for the expression of GFAP and S100 protein in both tumour cells and FS cells, in close relationship with hormone profile, and correlated with vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR) expression, previously studied by our team.

Results: GFAP and S100 protein were expressed both in tumour cells and FS cells. Differences between morphology, distribution, and density of GFAP+ FS cells and S100+ FS cells were observed according to the hormone profile of pituitary adenomas. GFAP and S100 protein expression in tumour cells was significantly related to hormone profile of pituitary adenomas and also with VEGF and EGFR expression.

Conclusions: GFAP and S100 protein expressions in tumour cells from pituitary adenomas are influenced by hormone profile. Our re­sults support the presence of two molecular subtypes of FS cells GFAP+/VEGF+/S100 respectively and another one that is GFAP-/S100+/EGFR+ simultaneously with the classical variant GFAP+/S100+. It is possible that S100+/EGFR+ pituitary adenomas represent a group of pituitary adenomas with an aggressive behaviour and a high ability of invasion and recurrence.

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Keywords

S100 protein, GFAP, folliculostellate cells, pituitary adenomas

About this article
Title

The “game” of glial fibrillary acidic and S100 proteins in pituitary adenomas: two players or several?

Journal

Endokrynologia Polska

Issue

Vol 68, No 4 (2017)

Article type

Original paper

Pages

380-389

Published online

2017-05-26

Page views

2069

Article views/downloads

1670

DOI

10.5603/EP.a2017.0029

Pubmed

28660986

Bibliographic record

Endokrynol Pol 2017;68(4):380-389.

Keywords

S100 protein
GFAP
folliculostellate cells
pituitary adenomas

Authors

Anca Maria Cimpean
Amalia Raluca Ceausu
Ana Corlan
Eugen Melnic
Andreea Adriana Jitariu
Marius Raica

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