Deciphering novel mitochondrial signatures: multi-omics analysis uncovers cross-disease markers and oligodendrocyte pathways in Alzheimer’s disease and glioblastoma

Our analysis identified four significant cross-disease mitochondrial markers: <i>EFHD1, SASH1, FAM110B,</i> and <i>SLC25A18</i>. These markers showed both shared and unique expression profiles in AD and GBM, suggesting a common mitochondrial mechanism contributing to both diseases. Additionally, oligodendrocytes and their interactions with astrocytes were implicated in disease progression, particularly through the APP signaling pathway. Key hub genes, such as <i>HS6ST3</i> and <i>TUBB2B</i>, were identified across different cellular subpopulations, highlighting a cell-specific co-expression network linked to mitochondrial function.

Authors

Institutions

Publication Details

Journal
Frontiers in Aging Neuroscience
Published
2025-02-13
DOI
https://doi.org/10.3389/fnagi.2025.1536142
Citations
3
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
2.42
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Deciphering novel mitochondrial signatures: multi-omics analysis uncovers cross-disease markers and oligodendrocyte pathways in Alzheimer’s disease and glioblastoma

Xiangyu Meng, Xuan Xu, Jiaqi Wang, Fei Wang et al.
3 citations
Frontiers in Aging Neuroscience
Mitochondrial Function and Pathology
2.42
article

Deciphering novel mitochondrial signatures: multi-omics analysis uncovers cross-disease markers and oligodendrocyte pathways in Alzheimer’s disease and glioblastoma

Xiangyu Meng, Xuan Xu, Jiaqi Wang, Fei Wang, Tong Chen, Shuaibin Wang, Yin Shen, Junwen He
article en
3 citations

Abstract

Our analysis identified four significant cross-disease mitochondrial markers: <i>EFHD1, SASH1, FAM110B,</i> and <i>SLC25A18</i>. These markers showed both shared and unique expression profiles in AD and GBM, suggesting a common mitochondrial mechanism contributing to both diseases. Additionally, oligodendrocytes and their interactions with astrocytes were implicated in disease progression, particularly through the APP signaling pathway. Key hub genes, such as <i>HS6ST3</i> and <i>TUBB2B</i>, were identified across different cellular subpopulations, highlighting a cell-specific co-expression network linked to mitochondrial function.

Frontiers in Aging NeuroscienceVol. 17
Minzu University of China (CN), Anhui Medical University (CN), Huazhong Agricultural University (CN)
Good health and well-being
Openalex Percentile: Top 13%
Mitochondrial Function and Pathology
2.42
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.