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Genome-wide expression datasets of anti-VEGF and dexamethasone treatment of angiogenesis in the rat cornea

Therapeutics against pathologic new blood vessel growth, particularly those targeting vascular endothelial growth factor (VEGF) are of enormous clinical interest. In the eye, where anti-VEGF agents are in widespread clinical use for treating retinal and corneal blindness, only partial or transient e...

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Autores principales: Mukwaya, Anthony, Mirabelli, Pierfrancesco, Lennikov, Anton, Xeroudaki, Maria, Schaupper, Mira, Peebo, Beatrice, Lagali, Neil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556618/
https://www.ncbi.nlm.nih.gov/pubmed/28809847
http://dx.doi.org/10.1038/sdata.2017.111
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author Mukwaya, Anthony
Mirabelli, Pierfrancesco
Lennikov, Anton
Xeroudaki, Maria
Schaupper, Mira
Peebo, Beatrice
Lagali, Neil
author_facet Mukwaya, Anthony
Mirabelli, Pierfrancesco
Lennikov, Anton
Xeroudaki, Maria
Schaupper, Mira
Peebo, Beatrice
Lagali, Neil
author_sort Mukwaya, Anthony
collection PubMed
description Therapeutics against pathologic new blood vessel growth, particularly those targeting vascular endothelial growth factor (VEGF) are of enormous clinical interest. In the eye, where anti-VEGF agents are in widespread clinical use for treating retinal and corneal blindness, only partial or transient efficacy and resistance to anti-VEGF agents are among the major drawbacks. Conversely, corticosteroids have long been used in ophthalmology for their potency in suppressing inflammation and angiogenesis, but their broad biological activity can give rise to side effects such as glaucoma and cataract. To aid in the search for more targeted and effective anti-angiogenic therapies in the eye, we present here a dataset comparing gene expression changes in dexamethasone versus anti-Vegfa treatment of inflammation leading to angiogenesis in the rat cornea. Global gene expression analysis with GeneChip Rat 230 2.0 microarrays was conducted and the metadata submitted to Expression Omnibus repository. Here, we present a high-quality validated dataset enabling genome-wide comparison of genes differentially targeted by dexamethasone and anti-Vegf treatments, to identify potential alternative therapeutic targets for evaluation.
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spelling pubmed-55566182017-08-30 Genome-wide expression datasets of anti-VEGF and dexamethasone treatment of angiogenesis in the rat cornea Mukwaya, Anthony Mirabelli, Pierfrancesco Lennikov, Anton Xeroudaki, Maria Schaupper, Mira Peebo, Beatrice Lagali, Neil Sci Data Data Descriptor Therapeutics against pathologic new blood vessel growth, particularly those targeting vascular endothelial growth factor (VEGF) are of enormous clinical interest. In the eye, where anti-VEGF agents are in widespread clinical use for treating retinal and corneal blindness, only partial or transient efficacy and resistance to anti-VEGF agents are among the major drawbacks. Conversely, corticosteroids have long been used in ophthalmology for their potency in suppressing inflammation and angiogenesis, but their broad biological activity can give rise to side effects such as glaucoma and cataract. To aid in the search for more targeted and effective anti-angiogenic therapies in the eye, we present here a dataset comparing gene expression changes in dexamethasone versus anti-Vegfa treatment of inflammation leading to angiogenesis in the rat cornea. Global gene expression analysis with GeneChip Rat 230 2.0 microarrays was conducted and the metadata submitted to Expression Omnibus repository. Here, we present a high-quality validated dataset enabling genome-wide comparison of genes differentially targeted by dexamethasone and anti-Vegf treatments, to identify potential alternative therapeutic targets for evaluation. Nature Publishing Group 2017-08-15 /pmc/articles/PMC5556618/ /pubmed/28809847 http://dx.doi.org/10.1038/sdata.2017.111 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ The Creative Commons Public Domain Dedication waiver http://creativecommons.org/publicdomain/zero/1.0/ applies to the metadata files made available in this article.
spellingShingle Data Descriptor
Mukwaya, Anthony
Mirabelli, Pierfrancesco
Lennikov, Anton
Xeroudaki, Maria
Schaupper, Mira
Peebo, Beatrice
Lagali, Neil
Genome-wide expression datasets of anti-VEGF and dexamethasone treatment of angiogenesis in the rat cornea
title Genome-wide expression datasets of anti-VEGF and dexamethasone treatment of angiogenesis in the rat cornea
title_full Genome-wide expression datasets of anti-VEGF and dexamethasone treatment of angiogenesis in the rat cornea
title_fullStr Genome-wide expression datasets of anti-VEGF and dexamethasone treatment of angiogenesis in the rat cornea
title_full_unstemmed Genome-wide expression datasets of anti-VEGF and dexamethasone treatment of angiogenesis in the rat cornea
title_short Genome-wide expression datasets of anti-VEGF and dexamethasone treatment of angiogenesis in the rat cornea
title_sort genome-wide expression datasets of anti-vegf and dexamethasone treatment of angiogenesis in the rat cornea
topic Data Descriptor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556618/
https://www.ncbi.nlm.nih.gov/pubmed/28809847
http://dx.doi.org/10.1038/sdata.2017.111
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