Evidence map›Paper›PMID 39702720›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

A Network Biology-Guided Investigation of the Long Noncoding RNAs' Role in Glaucoma.

Jyoti Kant Choudhari, Julio Vera, Tanushree Chatterjee

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Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jyoti Kant ChoudhariDepartment of Mathematics, Bioinformatics & Computer Applications Maulana Azad National Institute of Technology, Bhopal, Madhya Pradesh, India.
Julio VeraLaboratory of Systems Tumor Immunology, Department of Dermatology, Universitätsklinikum Erlangen and Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany. julio.vera-gonzalez@uk-erlangen.de.
Tanushree ChatterjeeDepartment of Biotechnology, Raipur Institute of Technology, Raipur, Chhattisgarh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glaucoma is a group of eye diseases characterized by progressive harm to the optic nerve that often results in loss of vision and blindness. Recent studies suggest that deregulation in the expression of a particular type of RNAs named long noncoding RNAs (lncRNAs) can impact the development of glaucoma and, hence, are promising targets for drug discovery. LncRNAs are transcripts with a length longer than 200 nucleotides that are not translated into proteins. Their extended length differentiates them from other non-coding RNAs such as microRNAs. Furthermore, lncRNAs exhibit diverse and often unpredictable regulatory functions within gene networks, unlike the well-defined gene silencing role of microRNAs. This chapter aims to discuss the role of lncRNAs in the pathogenesis of glaucoma. We will discuss and investigate lncRNAs linked to glaucoma, examine their functional regulation mechanisms in (glaucoma) gene networks, the extent of their (abnormal) expression in the disease, and their prospective as therapeutic targets. To this end, we performed lncRNA expression analysis from publicly available datasets and utilized this information to investigate their role in key pathways and biological mechanisms contributing to glaucoma progression. We employed a computational pipeline to construct glaucoma-associated lncRNA-miRNA, miRNA-TFs, gene-miRNA, protein-TF, and TF-TFs gene networks and used them to identify lncRNAs biomarkers for early diagnosis and disease progression monitoring. We identified lncRNA-enriched regulatory clusters and explored the potential of some of these lncRNA-gene clusters as targets for new therapies for glaucoma. Using this approach, we expect to give initial steps towards the elucidation of lncRNAs' role in glaucoma onset and progression.

Indexed as

Computational BiologyGene Regulatory NetworksGlaucomaMicroRNAsRNA, Long NoncodingGene Expression ProfilingGene Expression RegulationHumansTranscription FactorsMicroRNAsRNA, Long NoncodingTranscription FactorsBiomarkersDifferential expressionFunction mechanismsGlaucomaLong noncoding RNAsOcular diseasesPathogenesisTherapeutic potential

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.