Lens Proteomics Provide Novel Clues for Cataractogenesis: Original Investigation and a Broad Literature Survey

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Özet

Background: Previous proteomic studies provided valuable information about cataracts, but unclarified issues, such as sex and ethnicity-associated differences, remain. This study aimed to provide additional data on cataract-related proteins regarding age, sex, and cataract type. Methods: Twenty-six female and seven male Turkish cataract patients were screened for visual acuity and dysfunctional lens index. A nano-LC-MS/MS system and Progenesis QI software v3.0 were used for protein identification and quantification. The remaining data were evaluated with SPSS Version 29.0 software. Results: Proteins that showed age-associated changes were mainly involved in cytoskeletal organization. A glyoxalase enzyme, caveolin 1, and HS90B were lower, and RAB8B and ATP6V1B1 were higher in lenses in women. Proteins with lower levels in cataractous lenses than in transparent lenses included filensin and phakinin, concurrent with previous publications, and LCTL, GDI, HSPB1, and EIF4A2, not reported before. Corticonuclear cataracts constituted the only group showing depletions in putatively protective proteins, while the cortical type was the least influenced. ANXA1 and DNHD1 positively, and TCPD, SEC14L2, and PRPS1 proteins negatively correlated with visual acuity. Conclusions: This study revealed cataract-related proteins concurrent with earlier studies and new ones hitherto unreported. Despite the low number of patients investigated, the results merit further research, as these new proteins are highly likely to be involved in cataractogenesis.

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https://rdlopen.rawdatalibrary.net/r/kostu/10532Resmi atıflarda kullanılan kalıcı adres
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https://doi.org/10.3390/jcm14134737Yayıncı resmi DOI adresi
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AlanDeğerDil
dc.contributor.authorCosar, Banu
dc.contributor.authorNefesoglu, Mustafa Sehvar
dc.contributor.authorAltinoz, Meric A.
dc.contributor.authorAkgun, Emel
dc.contributor.authorSahin, Betul
dc.contributor.authorBaykal, Ahmet
dc.contributor.authorSerteser, Mustafa
dc.date.accessioned2026-10-27T23:47:37.073768786Z
dc.date.available2026-10-27T23:47:37.073768786Z
dc.date.issued2025
dc.description.abstractBackground: Previous proteomic studies provided valuable information about cataracts, but unclarified issues, such as sex and ethnicity-associated differences, remain. This study aimed to provide additional data on cataract-related proteins regarding age, sex, and cataract type. Methods: Twenty-six female and seven male Turkish cataract patients were screened for visual acuity and dysfunctional lens index. A nano-LC-MS/MS system and Progenesis QI software v3.0 were used for protein identification and quantification. The remaining data were evaluated with SPSS Version 29.0 software. Results: Proteins that showed age-associated changes were mainly involved in cytoskeletal organization. A glyoxalase enzyme, caveolin 1, and HS90B were lower, and RAB8B and ATP6V1B1 were higher in lenses in women. Proteins with lower levels in cataractous lenses than in transparent lenses included filensin and phakinin, concurrent with previous publications, and LCTL, GDI, HSPB1, and EIF4A2, not reported before. Corticonuclear cataracts constituted the only group showing depletions in putatively protective proteins, while the cortical type was the least influenced. ANXA1 and DNHD1 positively, and TCPD, SEC14L2, and PRPS1 proteins negatively correlated with visual acuity. Conclusions: This study revealed cataract-related proteins concurrent with earlier studies and new ones hitherto unreported. Despite the low number of patients investigated, the results merit further research, as these new proteins are highly likely to be involved in cataractogenesis.
dc.identifier.articlenumber4737
dc.identifier.doi10.3390/jcm14134737
dc.identifier.eissn2077-0383
dc.identifier.issn2077-0383
dc.identifier.issue13
dc.identifier.pmcidPMC12251298
dc.identifier.pmid40649110
dc.identifier.scopus2-s2.0-105019669071
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/kostu/10532
dc.identifier.volume14
dc.identifier.wosWOS:001526106100001
dc.language.isoen
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.ispartofJournal of Clinical Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectcataract
dc.subjectdysfunctional lens index
dc.subjectproteomics
dc.subjectvisual acuity
dc.subject.classificationMedicine, General & Internal
dc.subject.classificationGeneral & Internal Medicine
dc.subject.othercaveolin 1
dc.subject.otherfilensin
dc.subject.otherheat shock protein 27
dc.subject.otheradult
dc.subject.otherArticle
dc.subject.othercataract
dc.subject.othercataractogenesis
dc.subject.otherclinical feature
dc.subject.otherfemale
dc.subject.otherhealth care survey
dc.subject.otherhuman
dc.subject.otherlens implantation
dc.subject.otherliquid chromatography-mass spectrometry
dc.subject.othermajor clinical study
dc.subject.othermale
dc.subject.othermiddle aged
dc.subject.otherprotein analysis
dc.subject.otherproteomics
dc.subject.othervisual acuity
dc.titleLens Proteomics Provide Novel Clues for Cataractogenesis: Original Investigation and a Broad Literature Survey
dc.typeArticle
rdl.citation.openalex4
rdl.citation.scopus4
rdl.citation.wos4
rdl.departmentFaculty of Medicine, Department of Ophthalmology, Acibadem Mehmet Ali Aydınlar University, Istanbul 34398, Türkiye
rdl.departmentAvrupa Vocational School, Kocaeli Health and Technology University, Kocaeli 41001, Türkiye
rdl.departmentOphthalmology Clinic, Atasehir Florence Nightingale Hospital, Istanbul 34750, Türkiye
rdl.departmentFaculty of Medicine, Department of Medical Biochemistry, Acibadem Mehmet Ali Aydınlar University, Istanbul 34638, Türkiye
rdl.departmentAcıbadem LabMed Clinical Laboratories, Istanbul 34752, Türkiye
rdl.departmentDepartment of Biochemistry, Bahcesir University, Istanbul 34349, Türkiye
rdl.oa.statusgold
rdl.oa.statusgreen
rdl.oa.urlhttps://www.mdpi.com/2077-0383/14/13/4737/pdf?version=1751620934
rdl.scopus.quartileQ2
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)