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RNA sequencing and bioinformatics analysis of blood from patients with cortical cataracts.

Overview

Authors: Qian Li1, Lili Zhu2
  1. Department of Ophthalmology, The First People’s Hospital of Yuhang District, Hangzhou, China
  2. Department of Ophthalmology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310000 China
Journal: BMC ophthalmology, volume 26, issue 1, article 231
Dates: received 7 February 2026; accepted 20 March 2026; published online 26 March 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1186/s12886-026-04764-2 · PMID 41888716 · PMCID PMC13141249 · OpenAlex W7140402920
Open access: gold, a free copy (OpenAlex)
Categories: genetics / omics (modality), human (organism), clinical / translational (subfield)
Methods: Statistics, Graphs
Keywords: Cortical cataract, RNA-seq, GSEA, MPO
MeSH: Cataract*, Computational Biology*, Peroxidase*, Sequence Analysis, RNA*, Aged, Biomarkers, Enzyme-Linked Immunosorbent Assay, Female, Fibronectins, Gene Expression Profiling, Humans, Interleukin-8, Male, Middle Aged (* major topic)
Topic: Connexins and lens biology (Molecular Biology, Biochemistry, Genetics and Molecular Biology), according to OpenAlex
Citations: not cited yet (Europe PMC); 41 references in the paper

Abstract

The cortical cataract is the primary type of age-related cataract and can cause severe vision impairment in the early stage. To explore potential blood markers associated with individual physical conditions in cataract patients, we performed RNA sequencing to compare the differentially expressed genes (DEGs) between cortical and refractive cataract patients. Gene Ontology (GO) enrichment analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis, and gene set enrichment analysis (GSEA) were conducted. ELISA was subsequently used to validate differences in the protein expression levels of the selected genes. A total of 311 upregulated and 268 downregulated genes were identified. After bioinformatics analysis, we identified three key DEGs (MPO, CXCL8, and FN1) and determined their possible molecular mechanisms. As determined by ELISA, the expression of these genes increased; among them, MPO was the most significant DEG, and it related to oxidative stress responses through peroxidase activity and the catabolism of hydrogen peroxide. In conclusion, MPO, CXCL8 and FN1 were regarded as potential blood markers in patients. However, owing to the small sample size, the above conclusions are hypothetical.

Supplementary Information: The online version contains supplementary material available at 10.1186/s12886-026-04764-2.

Reproduced under the paper's license (CC BY), from the paper cited above.

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Data

Datasets cited

Data availability

The datasets generated during and/or analysed during the current study are available from the following. https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE308087. The Reviewer token: qdcpiaeqrbmbxqh

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

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Version 1, 30 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 2 authors, 4 keywords, 14 MeSH terms, 41 references.

Cite

This paper

Li, Q., & Zhu, L. (2026). RNA sequencing and bioinformatics analysis of blood from patients with cortical cataracts. BMC ophthalmology, 26(1), 231. https://doi.org/10.1186/s12886-026-04764-2

BibTeX

@article{li2026rna,
author = {Li, Qian and Zhu, Lili},
title = {{RNA sequencing and bioinformatics analysis of blood from patients with cortical cataracts}},
journal = {BMC ophthalmology},
year = {2026},
month = mar,
volume = {26},
number = {1},
pages = {231},
publisher = {BMC},
issn = {1471-2415},
doi = {10.1186/s12886-026-04764-2},
url = {https://doi.org/10.1186/s12886-026-04764-2},
pmid = {41888716},
pmcid = {PMC13141249}
}

RIS

TY - JOUR
AU - Li, Qian
AU - Zhu, Lili
TI - RNA sequencing and bioinformatics analysis of blood from patients with cortical cataracts
T2 - BMC ophthalmology
J2 - BMC Ophthalmol
PY - 2026
DA - 2026/03/26
VL - 26
IS - 1
SP - 231
SN - 1471-2415
PB - BMC
DO - 10.1186/s12886-026-04764-2
UR - https://doi.org/10.1186/s12886-026-04764-2
LA - en
ER -

CSL-JSON

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