<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang L</submitter><funding>Scientific Research Foundation for the Returned Overseas Chinese Scholars</funding><funding>Technology Innovation Project of Colleges and Universities in Shanxi Province</funding><funding>Medical major Research program of Shanxi</funding><funding>Major Research and Development Program of Shanxi</funding><pagination>16849</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12081695</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>Age-related macular degeneration (AMD) is the leading cause of vision loss in the elderly, and the role of chaperonin containing TCP1 subunit 2 (CCT2) remains unclear. This study aims to elucidate the mechanistic link between CCT2 and AMD, contributing to improved understanding and potential therapeutic strategies. Retinal and RPE-Choroid transcriptome array data from 130 AMD patients and 121 normal donors (GSE29801 dataset) were reanalyzed to assess CCT2 expression across different AMD subtypes, age groups, and genders. Single-sample gene set enrichment analysis was performed to explore correlations with autophagy-related genes and other established AMD causes. Additionally, CCT2 expression was validated in sodium iodate (NaIO₃)-induced 661 W cells (photoreceptor-like cells) using quantit</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Clinical characterization of CCT2 and its role in autophagy regulation during age-related macular degeneration.</pubmed_title><pmcid>PMC12081695</pmcid><funding_grant_id>No2020RC22</funding_grant_id><funding_grant_id>No. 2020-195</funding_grant_id><funding_grant_id>2022L203</funding_grant_id><funding_grant_id>No201903D321117</funding_grant_id><pubmed_authors>Li MY</pubmed_authors><pubmed_authors>Zhou GH</pubmed_authors><pubmed_authors>Wang LX</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Wang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical characterization of CCT2 and its role in autophagy regulation during age-related macular degeneration.</name><description>Age-related macular degeneration (AMD) is the leading cause of vision loss in the elderly, and the role of chaperonin containing TCP1 subunit 2 (CCT2) remains unclear. This study aims to elucidate the mechanistic link between CCT2 and AMD, contributing to improved understanding and potential therapeutic strategies. Retinal and RPE-Choroid transcriptome array data from 130 AMD patients and 121 normal donors (GSE29801 dataset) were reanalyzed to assess CCT2 expression across different AMD subtypes, age groups, and genders. Single-sample gene set enrichment analysis was performed to explore correlations with autophagy-related genes and other established AMD causes. Additionally, CCT2 expression was validated in sodium iodate (NaIO₃)-induced 661 W cells (photoreceptor-like cells) using quantit</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-04-08T19:52:54.338Z</modification><creation>2026-04-08T14:31:30.819Z</creation></dates><accession>S-EPMC12081695</accession><cross_references><pubmed>40374738</pubmed><doi>10.1038/s41598-025-01907-1</doi></cross_references></HashMap>