Determination of ADP/ATP translocase isoform ratios in malignancy and cellular senescence.
Ontology highlight
ABSTRACT: Cellular senescence has recently been recognized as a significant contributor to the poor prognosis of glioblastoma, one of the most aggressive brain tumors. Consequently, effectively eliminating senescent glioblastoma cells could benefit patients. Human ADP/ATP translocases (ANTs) play a role in oxidative phosphorylation in both normal and tumor cells. Previous research has shown that the sensitivity of senescent cells to mitochondria-targeted senolytics depends on the level of ANT2. Here, we systematically mapped the transcript and protein levels of ANT isoforms in various types of senescence and glioblastoma tumorigenesis. We employed bioinformatics analysis, targeted mass spectrometry, RT-PCR, immunoblotting, and assessment of cellular energy state to elucidate how individual ANT isofo
SUBMITTER: Liblova Z
PROVIDER: S-EPMC12420346 | biostudies-literature | 2025 Sep
REPOSITORIES: biostudies-literature
ACCESS DATA