Expression of the Annexin A1 and its correlation with matrix metalloproteinases and the receptor for formylated peptide-2 in diffuse astrocytic tumors

Astrocytomas represent the majority of cerebral gliomas. Studies show that the anti-inflammatory protein Annexin-A1 (ANXA1) is associated with the tumor invasion process and that its actions can be mediated by the receptor for formylated peptides (FPR). Therefore, we evaluated the expression of ANXA...

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Published in:Annals of diagnostic pathology Vol. 37; pp. 62 - 66
Main Authors: Tadei, Maryam Buainain, Mayorquim, Matheus Vicente, de Souza, Camila Brambilla, de Souza Costa, Sara, Possebon, Lucas, Souza, Helena Ribeiro, Iyomasa-Pilon, Melina Mizusaki, Geromel, Mairto Roberis, Girol, Ana Paula
Format: Journal Article
Language:English
Published: United States Elsevier Inc 01-12-2018
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Abstract Astrocytomas represent the majority of cerebral gliomas. Studies show that the anti-inflammatory protein Annexin-A1 (ANXA1) is associated with the tumor invasion process and that its actions can be mediated by the receptor for formylated peptides (FPR). Therefore, we evaluated the expression of ANXA1, the receptor FPR2 and matrix metalloproteinases 2 and 9 (MMP-2 and MMP-9) in brain astrocytomas. Detection of proteins was performed in sections of diffuse astrocytomas (grade II), anaplastic astrocytomas (grade III) and glioblastomas (GBM, grade IV) and quantifications were made by densitometry. Our analyses showed increased expression of ANXA1 in astrocytomas of all grades, but especially in GBM. The expression of FPR2 is similar to that found for ANXA1, being higher in GBM. Immunostaining for MMPs is also stronger as the degree of malignancy increases, especially with respect to MMP-9. The positive correlation between ANXA1/FPR2 and ANXA1/MMP-9 was observed in all tumors studied. The data indicate the possible action of ANXA1 and FPR2 on the development and progression of astrocytomas, related to increased expression of MMP-9. Thereby, ANXA1 and FPR2 are involved in the biology and malignancy of diffuse astrocytic tumors. •ANXA1, FPR2, MMP2 and MMP9 increase accordingly the malignant grade in diffuse astrocytic tumors.•ANXA1, FPR2, MMP2 and MMP9 are overexpressed in GBM.•ANXA1/FPR2 and ANXA1/MMP9 are positively correlated in diffuse astrocytic tumors grades II, III and IV.•ANXA1 is related to increased expression of MMPs in diffuse astrocytic tumors.•ANXA1 and FPR2 may be associated with malignancy phenotype in GBM.
AbstractList Astrocytomas represent the majority of cerebral gliomas. Studies show that the anti-inflammatory protein Annexin-A1 (ANXA1) is associated with the tumor invasion process and that its actions can be mediated by the receptor for formylated peptides (FPR). Therefore, we evaluated the expression of ANXA1, the receptor FPR2 and matrix metalloproteinases 2 and 9 (MMP-2 and MMP-9) in brain astrocytomas. Detection of proteins was performed in sections of diffuse astrocytomas (grade II), anaplastic astrocytomas (grade III) and glioblastomas (GBM, grade IV) and quantifications were made by densitometry. Our analyses showed increased expression of ANXA1 in astrocytomas of all grades, but especially in GBM. The expression of FPR2 is similar to that found for ANXA1, being higher in GBM. Immunostaining for MMPs is also stronger as the degree of malignancy increases, especially with respect to MMP-9. The positive correlation between ANXA1/FPR2 and ANXA1/MMP-9 was observed in all tumors studied. The data indicate the possible action of ANXA1 and FPR2 on the development and progression of astrocytomas, related to increased expression of MMP-9. Thereby, ANXA1 and FPR2 are involved in the biology and malignancy of diffuse astrocytic tumors.
Astrocytomas represent the majority of cerebral gliomas. Studies show that the anti-inflammatory protein Annexin-A1 (ANXA1) is associated with the tumor invasion process and that its actions can be mediated by the receptor for formylated peptides (FPR). Therefore, we evaluated the expression of ANXA1, the receptor FPR2 and matrix metalloproteinases 2 and 9 (MMP-2 and MMP-9) in brain astrocytomas. Detection of proteins was performed in sections of diffuse astrocytomas (grade II), anaplastic astrocytomas (grade III) and glioblastomas (GBM, grade IV) and quantifications were made by densitometry. Our analyses showed increased expression of ANXA1 in astrocytomas of all grades, but especially in GBM. The expression of FPR2 is similar to that found for ANXA1, being higher in GBM. Immunostaining for MMPs is also stronger as the degree of malignancy increases, especially with respect to MMP-9. The positive correlation between ANXA1/FPR2 and ANXA1/MMP-9 was observed in all tumors studied. The data indicate the possible action of ANXA1 and FPR2 on the development and progression of astrocytomas, related to increased expression of MMP-9. Thereby, ANXA1 and FPR2 are involved in the biology and malignancy of diffuse astrocytic tumors. •ANXA1, FPR2, MMP2 and MMP9 increase accordingly the malignant grade in diffuse astrocytic tumors.•ANXA1, FPR2, MMP2 and MMP9 are overexpressed in GBM.•ANXA1/FPR2 and ANXA1/MMP9 are positively correlated in diffuse astrocytic tumors grades II, III and IV.•ANXA1 is related to increased expression of MMPs in diffuse astrocytic tumors.•ANXA1 and FPR2 may be associated with malignancy phenotype in GBM.
Author de Souza Costa, Sara
Possebon, Lucas
Iyomasa-Pilon, Melina Mizusaki
Mayorquim, Matheus Vicente
Geromel, Mairto Roberis
Tadei, Maryam Buainain
Souza, Helena Ribeiro
de Souza, Camila Brambilla
Girol, Ana Paula
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/30286327$$D View this record in MEDLINE/PubMed
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Keywords FPR
Glioblastomas
Astrocytomas
Annexin A1
Metalloproteinases
Language English
License Copyright © 2018 Elsevier Inc. All rights reserved.
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Snippet Astrocytomas represent the majority of cerebral gliomas. Studies show that the anti-inflammatory protein Annexin-A1 (ANXA1) is associated with the tumor...
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SubjectTerms Annexin A1
Astrocytomas
FPR
Glioblastomas
Metalloproteinases
Title Expression of the Annexin A1 and its correlation with matrix metalloproteinases and the receptor for formylated peptide-2 in diffuse astrocytic tumors
URI https://dx.doi.org/10.1016/j.anndiagpath.2018.08.002
https://www.ncbi.nlm.nih.gov/pubmed/30286327
https://search.proquest.com/docview/2116849561
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