Association between NAT10 gene rs8187 G > A polymorphism and Wilms tumor susceptibility in Chinese Han children: a five-center case-control study
BMC Cancer,
Год журнала:
2025,
Номер
25(1)
Опубликована: Март 17, 2025
Wilms
tumor,
a
prevalent
pediatric
kidney
cancer,
has
been
extensively
studied
to
elucidate
its
genetic
mechanisms.
NAT10
(N-acetyltransferase
10)
is
gene
encoding
acetyltransferase,
which
involved
in
various
cellular
processes,
including
RNA
modification,
DNA
repair,
and
protein
acetylation.
The
oncogenic
role
of
cancer
garnered
significant
attention.
However,
research
on
variants
their
associations
with
nascent.
This
study
investigated
the
link
between
tumor
risk
via
case‒control
design
genomic
from
414
patients
1199
controls.
Genotyping
was
performed
TaqMan
method,
logistic
regression
statistical
analysis
conducted
identify
associations,
followed
by
extra
minimize
false
positive
results.
Our
findings
revealed
that
rs8187
G
>
A
polymorphism
significantly
correlated
decreased
developing
(GA
vs.
GG,
adjusted
odds
ratio
(AOR)
=
0.60,
95%
confidence
interval
(CI)
0.46-0.77,
P
<
0.0001;
GA/AA
AOR
0.74,
CI
0.59-0.93,
0.011).
Stratified
analyses
further
association
children
aged
18
months
or
under
subgroups
stage
II,
IV,
combined
I
+
II
tumors.
These
results
highlight
potential
as
markers
for
susceptibility.
clarifies
basis
susceptibility
highlights
early
detection
assessment.
Язык: Английский
Targeting NAT10 attenuates homologous recombination via destabilizing DNA:RNA hybrids and overcomes PARP inhibitor resistance in cancers
Drug Resistance Updates,
Год журнала:
2025,
Номер
unknown, С. 101241 - 101241
Опубликована: Март 1, 2025
Язык: Английский
Improvement of MASLD and MASH by suppression of hepatic N-Acetyltransferase 10
Molecular Metabolism,
Год журнала:
2024,
Номер
89, С. 102030 - 102030
Опубликована: Сен. 17, 2024
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
and
metabolic
steatohepatitis
(MASH)
are
characterized
by
excessive
triglyceride
accumulation
in
the
liver.
However,
due
to
an
incomplete
understanding
of
its
pathogenesis,
more
efforts
needed
identify
specific
effective
treatments.
N4-acetylcytidine
(ac4C)
is
a
newly
discovered
RNA
modification
regulate
mRNA.
N-acetyltransferase
10
(NAT10)
has
not
been
fully
explored
MASLD
MASH.
Язык: Английский
The role and mechanism of NAT10‐mediated ac4C modification in tumor development and progression
Zhuoran Gu,
Libin Zou,
Xinjian Pan
и другие.
MedComm,
Год журнала:
2024,
Номер
5(12)
Опубликована: Дек. 1, 2024
Abstract
RNA
modification
has
emerged
as
a
crucial
area
of
research
in
epigenetics,
significantly
influencing
tumor
biology
by
regulating
metabolism.
N‐acetyltransferase
10
(NAT10)‐mediated
N4‐acetylcytidine
(ac4C)
modification,
the
sole
known
acetylation
eukaryotic
RNA,
influences
cancer
pathogenesis
and
progression.
NAT10
is
only
writer
ac4C
catalyzes
acetyl
transfer
on
targeted
helps
to
improve
stability
translational
efficiency
ac4C‐modified
RNA.
highly
expressed
associated
with
poor
prognosis
pan‐cancers.
Based
its
molecular
mechanism
biological
functions,
central
factor
tumorigenesis,
progression,
drug
resistance,
immune
escape.
Despite
increasing
focus
ac4C,
specific
regulatory
mechanisms
remain
elusive.
The
present
review
thoroughly
analyzes
current
knowledge
NAT10‐mediated
cancer,
highlighting
broad
influence
gene
expression
biology.
This
also
summarizes
limitations
perspectives
identify
new
therapeutic
targets
advance
treatment
strategies.
Язык: Английский
Degron-modified Cas12a enhances single-cell CRISPR screening
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 8, 2024
Abstract
Single-cell
CRISPR
(Perturb-seq)
screens
have
primarily
relied
on
Cas9
whereas
Cas12a,
despite
its
unique
effectiveness
for
multiplex
guide
expression,
remains
underexplored.
This
may
be
due
to
Cas12a’s
RNA
array
(pre-crRNA)
self-processing
activity
and
the
subsequent
challenges
associated
with
pre-crRNA
sequence
recovery.
By
developing
modified
expression
vectors
a
degron-based
Cas12a
system,
we
overcome
constraint,
allowing
accurate
detection
of
pre-crRNAs
at
single-cell
level,
thus
greatly
expanding
possibilities
future
Perturb-seq
efforts.
Язык: Английский