New molecular aspects of the pathogenesis of osteoporosis – perspectives for early diagnosis and treatment DOI Creative Commons
Anton Tyurin,

Karina E. Akhiyarova,

Bulat I. Yalaev

и другие.

Modern Rheumatology Journal, Год журнала: 2024, Номер 18(2), С. 103 - 110

Опубликована: Апрель 22, 2024

Osteoporosis (OP) is a common disease leading to low-trauma fractures and serious medical social problem. Often fracture the first clinical manifestation of OP that has been asymptomatic for long time, necessitating development methods early detection risk assessment this disease. multifactorial with strong hereditary component. However, as data from study genetic factors show, only 15% heritability trait can be explained. In context, focus research shifting area epigenetic regulation, which controls gene activity without altering primary structure DNA. One most promising mechanisms control methylation, affects DNA well RNA histones. The characteristics these possibilities their use diagnosis treatment are presented in review.

Язык: Английский

m6A modifications of circular RNAs in ischemia-induced retinal neovascularization DOI Creative Commons
Yedi Zhou, Bingyan Li,

Zicong Wang

и другие.

International Journal of Medical Sciences, Год журнала: 2023, Номер 20(2), С. 254 - 261

Опубликована: Янв. 1, 2023

Ischemia-induced pathological neovascularization in the retina is a leading cause of blindness various age groups. The purpose current study was to identify involvement circular RNAs (circRNAs) methylated by N6-methyladenosine (m6A), and predict their potential roles oxygen-induced retinopathy (OIR) mice. Methylation assessment via microarray analysis indicated that 88 circRNAs were differentially modified m6A methylation, including 56 hyper-methylated 32 hypo-methylated circRNAs. Gene ontology enrichment predicted enriched host genes involved cellular process, anatomical entity, protein binding. Host regulation biosynthetic nucleus, According Kyoto Encyclopedia Genes Genomes analysis, those pathways selenocompound metabolism, salivary secretion, lysine degradation. MeRIP-qPCR verified significant alterations methylation levels mmu_circRNA_33363, mmu_circRNA_002816, mmu_circRNA_009692. In conclusion, revealed modification OIR retinas, findings above shed light on circRNA regulatory functions pathogenesis ischemia-induced retinal neovascularization.

Язык: Английский

Процитировано

3

Identification of ROCK1 as a novel biomarker for postmenopausal osteoporosis and pan-cancer analysis DOI Creative Commons
Bo-Wen Lai, Heng Jiang, Yuan Gao

и другие.

Aging, Год журнала: 2023, Номер 15(17), С. 8873 - 8907

Опубликована: Сен. 7, 2023

Postmenopausal osteoporosis (PMOP) is a prevalent bone disorder with significant global impact. The elevated risk of osteoporotic fracture in elderly women poses substantial burden on individuals and society. Unfortunately, the current lack dependable diagnostic markers precise therapeutic targets for PMOP remains major challenge.PMOP-related datasets GSE7429, GSE56814, GSE56815, GSE147287, were downloaded from GEO database. DEGs identified by "limma" packages. WGCNA Machine Learning used to choose key module genes highly related PMOP. GSEA, DO, GO, KEGG enrichment analysis was performed all selected hub genes. PPI network constructed through GeneMANIA ROC curves AUC values validated both training validation datasets. xCell immune infiltration single-cell genes' function reaction Pan-cancer revealed role cancers.A total 1278 between patients healthy controls. purple cyan as modules 112 common after combining Five algorithms screened three (KCNJ2, HIPK1, ROCK1), validate ROCK1 (AUC = 0.73) 0.81). GSEA low-ROCK1 patients, top enriched field included protein binding reaction. DCs NKT cells expressed showed correlation low expression SKCM well renal tumors (KIRP, KICH, KIRC).ROCK1 significantly associated pathogenesis PMOP, influenced cancer development, progression, prognosis, which provided potential therapy target tumors. However, further laboratory clinical evidence required before application target.

Язык: Английский

Процитировано

3

SALL1 promotes proliferation and metastasis and activates phosphorylation of p65 and JUN in colorectal cancer cells DOI
Jie Yuan, Guiying Li, Fei Zhong

и другие.

Pathology - Research and Practice, Год журнала: 2023, Номер 250, С. 154827 - 154827

Опубликована: Сен. 21, 2023

Язык: Английский

Процитировано

2

Analysis of N6-Methyladenosine RNA Methylation Regulators in Diagnosis and Distinct Molecular Subtypes of Ankylosing Spondylitis DOI Creative Commons
Cheng Zhong, Jiahua Liang, Zhen Chen

и другие.

Disease Markers, Год журнала: 2022, Номер 2022, С. 1 - 23

Опубликована: Сен. 16, 2022

The most frequent internal modification in eukaryotic mRNA is N6-methyladenosine (m6A). However, what we know about the m6A regulators Ankylosing spondylitis (AS) still limited. In our study, eight distinct were selected utilizing Differentially Expressed Gene (DEG) analysis of Expression Omnibus GSE73754 dataset for making comparisons between AS (Ankylosing spondylitis) and non-AS patients. random forest model nomogram used to screen candidate evaluate their prediction accuracy occurrence AS. Furthermore, based on regulators, patients divided into two subgroups, applied principal component algorithms calculate score patterns. Our findings revealed that cluster A linked activated CD4 T cell immunity CD8 immunity. With its major contributions area immunology, research patterns may benefit future diagnosis treatment strategies

Язык: Английский

Процитировано

3

New molecular aspects of the pathogenesis of osteoporosis – perspectives for early diagnosis and treatment DOI Creative Commons
Anton Tyurin,

Karina E. Akhiyarova,

Bulat I. Yalaev

и другие.

Modern Rheumatology Journal, Год журнала: 2024, Номер 18(2), С. 103 - 110

Опубликована: Апрель 22, 2024

Osteoporosis (OP) is a common disease leading to low-trauma fractures and serious medical social problem. Often fracture the first clinical manifestation of OP that has been asymptomatic for long time, necessitating development methods early detection risk assessment this disease. multifactorial with strong hereditary component. However, as data from study genetic factors show, only 15% heritability trait can be explained. In context, focus research shifting area epigenetic regulation, which controls gene activity without altering primary structure DNA. One most promising mechanisms control methylation, affects DNA well RNA histones. The characteristics these possibilities their use diagnosis treatment are presented in review.

Язык: Английский

Процитировано

0