ACSS2/AATF Drives Soluble FasL‐Mediated CD8+ T Cell Apoptosis in Pancreatic Neuroendocrine Tumors
This study unveils that ACSS2‐driven acetate metabolism fuels histone pan‐acetylation in pancreatic neuroendocrine tumors (PNETs), remodeling the epigenetic landscape. The ACSS2/AATF axis transcriptionally activates soluble FasL (sFasL), which engages Fas receptors on infiltrating CD8+ T cells to trigger caspase‐8/3‐mediated apoptosis.
Qin Dang +14 more
wiley +1 more source
SAT1 promotes the progression of OA by regulating TRIM33-mediated p53 acetylation to enhance ferroptosis. [PDF]
Yang J, Jiang J, Wang J, Luo L.
europepmc +1 more source
On the Studies of Reactivity of Pulps for Acetylation
Saburō Ishikawa
openalex +2 more sources
The artificial biosynthetic pathway potentially involved in biosynthesis of enfumafungin is first reconstructed in an optimized Aspergillus oryzae chassis with the increased site‐specific integration efficiency and shortened time for marker recycling, which requires an artificial fusion enzyme EfuA(TC)FsoA(GT).
Yaohui Gao +11 more
wiley +1 more source
From allergens to epigenetics: how histone acetylation shapes immune gene expression in allergic diseases. [PDF]
Cai X +5 more
europepmc +1 more source
LIQUID PHASE FIBROUS ACETYLATION OF CELLULOSE
Ichiro Sakurada +2 more
openalex +2 more sources
H3K27ac Is Essential for Human Naive Pluripotency Modulated by m6A‐Driven EP300 Expression
An et al. reveal H3K27ac elevation is essential for establishing and maintaining human naive pluripotency; its inhibition disrupts this state while enhancement promotes it. METTL3‐mediated m6A modification indirectly controls H3K27ac by suppressing EP300 expression. Reduced EP300 lowers H3K27ac, impeding naive pluripotency.
Chenrui An +13 more
wiley +1 more source
MRPL12 K163 acetylation inhibits ccRCC via driving mitochondrial metabolic reprogramming. [PDF]
Ji X +10 more
europepmc +1 more source
STUDIES ON THE VAPOUR PHASE ACETYLATION OF CELLULOSE
Iichiro Kido +2 more
openalex +2 more sources
Hepatic CBP/p300 Orchestrate Amino Acid‐Driven Gluconeogenesis through Histone Crotonylation
Hepatic CBP/p300 control amino acid‐driven gluconeogenesis by modulating histone crotonylation. This study identifies 2‐aminoadipate (2‐AAA) as a key metabolite that enhances crotonylation and activates amino acid and gluconeogenic gene expression.
Chunxiang Sheng +15 more
wiley +1 more source

