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Preliminary study of hypoxia markers in diffuse large B-cell lymphoma
While the association of hypoxia has been established in various types of solid cancers, little is known about its presence and existence in diffuse large B-cell lymphoma (DLBCL). The purpose of the present study was to evaluate the expression of hypoxia-inducible factor-1α (HIF-1α) and vascular end...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353874/ https://www.ncbi.nlm.nih.gov/pubmed/35949890 http://dx.doi.org/10.3892/mco.2022.2573 |
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author | Pangarsa, Eko A. Wuryantoro, Probo Naibaho, Ridho M. Setiawan, Budi Santosa, Damai Istiadi, Hermawan Puspasari, Dik Suharti, Catharina |
author_facet | Pangarsa, Eko A. Wuryantoro, Probo Naibaho, Ridho M. Setiawan, Budi Santosa, Damai Istiadi, Hermawan Puspasari, Dik Suharti, Catharina |
author_sort | Pangarsa, Eko A. |
collection | PubMed |
description | While the association of hypoxia has been established in various types of solid cancers, little is known about its presence and existence in diffuse large B-cell lymphoma (DLBCL). The purpose of the present study was to evaluate the expression of hypoxia-inducible factor-1α (HIF-1α) and vascular endothelial growth factor A (VEGF-A) in DLBCL and to analyze the association of these factors with several clinical and pathological characteristics. The immunohistochemical protein expression of HIF-1α and VEGF-A was investigated in 34 de novo DLBCL tumor samples from January 2017 to December 2017 from the Department of Hematology/Medical Oncology and Anatomical Pathology at Dr Kariadi Hospital (Semarang, Indonesia). The present study revealed by using immunohistochemistry (IHC), that hypoxic markers were overexpressed (88.2% for both HIF-1α and VEGF-A) in the vast majority of patients with DLBCL. Only in 4 tumors, was HIF-1α expression normal, and interestingly VEGF-A was negative as well. There was a significant correlation in the intensity of staining of HIF-1α and VEGF-A using our custom scoring system in surgically resected tissues (r=0.475; P=0.005). Both HIF-1α and VEGF-A were also associated to serum LDH and tumor diameter. Collectively, HIF-1α and VEGF-A were predominantly expressed in the majority of DLBCL tumor cells. The findings of the present study indicate the existence of hypoxia in DLBCL tumors similar to numerous solid cancers, and thus warrants further investigation to clarify its role as a potential pathogenic or prognostic marker in this type of hematological cancer. |
format | Online Article Text |
id | pubmed-9353874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-93538742022-08-09 Preliminary study of hypoxia markers in diffuse large B-cell lymphoma Pangarsa, Eko A. Wuryantoro, Probo Naibaho, Ridho M. Setiawan, Budi Santosa, Damai Istiadi, Hermawan Puspasari, Dik Suharti, Catharina Mol Clin Oncol Articles While the association of hypoxia has been established in various types of solid cancers, little is known about its presence and existence in diffuse large B-cell lymphoma (DLBCL). The purpose of the present study was to evaluate the expression of hypoxia-inducible factor-1α (HIF-1α) and vascular endothelial growth factor A (VEGF-A) in DLBCL and to analyze the association of these factors with several clinical and pathological characteristics. The immunohistochemical protein expression of HIF-1α and VEGF-A was investigated in 34 de novo DLBCL tumor samples from January 2017 to December 2017 from the Department of Hematology/Medical Oncology and Anatomical Pathology at Dr Kariadi Hospital (Semarang, Indonesia). The present study revealed by using immunohistochemistry (IHC), that hypoxic markers were overexpressed (88.2% for both HIF-1α and VEGF-A) in the vast majority of patients with DLBCL. Only in 4 tumors, was HIF-1α expression normal, and interestingly VEGF-A was negative as well. There was a significant correlation in the intensity of staining of HIF-1α and VEGF-A using our custom scoring system in surgically resected tissues (r=0.475; P=0.005). Both HIF-1α and VEGF-A were also associated to serum LDH and tumor diameter. Collectively, HIF-1α and VEGF-A were predominantly expressed in the majority of DLBCL tumor cells. The findings of the present study indicate the existence of hypoxia in DLBCL tumors similar to numerous solid cancers, and thus warrants further investigation to clarify its role as a potential pathogenic or prognostic marker in this type of hematological cancer. D.A. Spandidos 2022-07-28 /pmc/articles/PMC9353874/ /pubmed/35949890 http://dx.doi.org/10.3892/mco.2022.2573 Text en Copyright: © Pangarsa et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Pangarsa, Eko A. Wuryantoro, Probo Naibaho, Ridho M. Setiawan, Budi Santosa, Damai Istiadi, Hermawan Puspasari, Dik Suharti, Catharina Preliminary study of hypoxia markers in diffuse large B-cell lymphoma |
title | Preliminary study of hypoxia markers in diffuse large B-cell lymphoma |
title_full | Preliminary study of hypoxia markers in diffuse large B-cell lymphoma |
title_fullStr | Preliminary study of hypoxia markers in diffuse large B-cell lymphoma |
title_full_unstemmed | Preliminary study of hypoxia markers in diffuse large B-cell lymphoma |
title_short | Preliminary study of hypoxia markers in diffuse large B-cell lymphoma |
title_sort | preliminary study of hypoxia markers in diffuse large b-cell lymphoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353874/ https://www.ncbi.nlm.nih.gov/pubmed/35949890 http://dx.doi.org/10.3892/mco.2022.2573 |
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