Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: Aug. 24, 2023
The
proper
transfer
of
genetic
information
from
DNA
to
RNA
protein
is
essential
for
cell-fate
control,
development,
and
health.
Methylation
DNA,
RNAs,
histones,
non-histone
proteins
a
reversible
post-synthesis
modification
that
finetunes
gene
expression
function
in
diverse
physiological
processes.
Aberrant
methylation
caused
by
mutations
or
environmental
stimuli
promotes
various
diseases
accelerates
aging,
necessitating
the
development
therapies
correct
disease-driver
imbalance.
In
this
Review,
we
summarize
operating
system
across
central
dogma,
which
includes
writers,
erasers,
readers,
reader-independent
outputs.
We
then
discuss
how
dysregulation
contributes
neurological
disorders,
cancer,
aging.
Current
small-molecule
compounds
target
modifiers
show
modest
success
certain
cancers.
methylome-wide
action
lack
specificity
lead
undesirable
biological
effects
cytotoxicity,
limiting
their
therapeutic
application,
especially
with
monogenic
cause
different
directions
changes.
Emerging
tools
capable
site-specific
manipulation
hold
great
promise
solve
dilemma.
With
refinement
delivery
vehicles,
these
new
are
well
positioned
advance
basic
research
clinical
translation
field.
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: May 13, 2023
Abstract
Infection
susceptibility,
poor
vaccination
efficacy,
age-related
disease
onset,
and
neoplasms
are
linked
to
innate
adaptive
immune
dysfunction
that
accompanies
aging
(known
as
immunosenescence).
During
aging,
organisms
tend
develop
a
characteristic
inflammatory
state
expresses
high
levels
of
pro-inflammatory
markers,
termed
inflammaging.
This
chronic
inflammation
is
typical
phenomenon
immunosenescence
it
considered
the
major
risk
factor
for
diseases.
Thymic
involution,
naïve/memory
cell
ratio
imbalance,
dysregulated
metabolism,
epigenetic
alterations
striking
features
immunosenescence.
Disturbed
T-cell
pools
antigen
stimulation
mediate
premature
senescence
cells,
senescent
cells
proinflammatory
senescence-associated
secretory
phenotype
exacerbates
Although
underlying
molecular
mechanisms
remain
be
addressed,
well
documented
T
inflammaging
might
driving
forces
in
Potential
counteractive
measures
will
discussed,
including
intervention
cellular
metabolic-epigenetic
axes
mitigate
In
recent
years,
has
attracted
increasing
attention
its
role
tumor
development.
As
result
limited
participation
elderly
patients,
impact
on
cancer
immunotherapy
unclear.
Despite
some
surprising
results
from
clinical
trials
drugs,
necessary
investigate
other
Signal Transduction and Targeted Therapy,
Journal Year:
2022,
Volume and Issue:
7(1)
Published: Nov. 7, 2022
Abstract
Aging
is
accompanied
by
the
decline
of
organismal
functions
and
a
series
prominent
hallmarks,
including
genetic
epigenetic
alterations.
These
aging-associated
changes
include
DNA
methylation,
histone
modification,
chromatin
remodeling,
non-coding
RNA
(ncRNA)
regulation,
all
which
participate
in
regulation
aging
process,
hence
contribute
to
aging-related
diseases.
Therefore,
understanding
mechanisms
will
provide
new
avenues
develop
strategies
delay
aging.
Indeed,
interventions
based
on
manipulating
have
led
alleviation
or
extension
lifespan
animal
models.
Small
molecule-based
therapies
reprogramming
that
enable
rejuvenation
been
developed
for
ameliorating
reversing
conditions.
In
addition,
adopting
health-promoting
activities,
such
as
caloric
restriction,
exercise,
calibrating
circadian
rhythm,
has
demonstrated
Furthermore,
various
clinical
trials
intervention
are
ongoing,
providing
more
evidence
safety
efficacy
these
therapies.
Here,
we
review
recent
work
outline
advances
age-associated
A
better
critical
roles
epigenetics
process
lead
prevention
human
therapy
Aging
is
a
complex
biological
process
characterized
by
hallmark
features
accumulating
over
the
life
course,
shaping
individual's
aging
trajectory
and
subsequent
disease
risks.
There
substantial
individual
variability
in
between
men
women.
In
general,
women
live
longer
than
men,
consistent
with
lower
ages
as
assessed
molecular
biomarkers,
but
there
paradox.
Women
are
frailer
have
worse
health
at
end
of
life,
while
still
perform
better
physical
function
examinations.
Moreover,
many
age-related
diseases
show
sex-specific
patterns.
this
review,
we
aim
to
summarize
current
knowledge
on
sexual
dimorphism
human
studies,
support
from
animal
research,
illnesses.
We
also
attempt
place
it
context
theories
aging,
well
discuss
explanations
for
sex
differences,
example,
sex-chromosome
linked
mechanisms
hormonally
driven
differences.
Signal Transduction and Targeted Therapy,
Journal Year:
2021,
Volume and Issue:
6(1)
Published: June 28, 2021
Remarkable
progress
in
ageing
research
has
been
achieved
over
the
past
decades.
General
perceptions
and
experimental
evidence
pinpoint
that
decline
of
physical
function
often
initiates
by
cell
senescence
organ
ageing.
Epigenetic
dynamics
immunometabolic
reprogramming
link
to
alterations
cellular
response
intrinsic
extrinsic
stimuli,
representing
current
hotspots
as
they
not
only
(re-)shape
individual
identity,
but
also
involve
fate
decision.
This
review
focuses
on
present
findings
emerging
concepts
epigenetic,
inflammatory,
metabolic
regulations
consequences
process.
Potential
therapeutic
interventions
targeting
regulatory
mechanisms,
using
state-of-the-art
techniques
are
discussed.
Nucleic Acids Research,
Journal Year:
2020,
Volume and Issue:
49(D1), P. D825 - D830
Published: Sept. 30, 2020
Organismal
aging
is
driven
by
interconnected
molecular
changes
encompassing
internal
and
extracellular
factors.
Combinational
analysis
of
high-throughput
'multi-omics'
datasets
(gathering
information
from
genomics,
epigenomics,
transcriptomics,
proteomics,
metabolomics
pharmacogenomics),
at
either
populational
or
single-cell
levels,
can
provide
a
multi-dimensional,
integrated
profile
the
heterogeneous
process
with
unprecedented
throughput
detail.
These
new
strategies
allow
for
exploration
regulatory
status
gene
expression
during
aging,
in
turn,
facilitate
development
interventions.
With
continually
growing
volume
valuable
aging-related
data,
it
necessary
to
establish
an
open
database
support
wide
spectrum
research.
The
Aging
Atlas
aims
range
life
science
researchers
resources
that
access
large-scale
regulation
created
various
omics
technologies.
current
implementation
includes
five
modules:
transcriptomics
(RNA-seq),
(scRNA-seq),
epigenomics
(ChIP-seq),
proteomics
(protein-protein
interaction),
pharmacogenomics
(geroprotective
compounds).
provides
user-friendly
functionalities
explore
age-related
expression,
as
well
raw
data
download
services.
freely
available
https://bigd.big.ac.cn/aging/index.
Cell,
Journal Year:
2023,
Volume and Issue:
186(2), P. 287 - 304.e26
Published: Jan. 1, 2023
Whether
and
how
certain
transposable
elements
with
viral
origins,
such
as
endogenous
retroviruses
(ERVs)
dormant
in
our
genomes,
can
become
awakened
contribute
to
the
aging
process
is
largely
unknown.
In
human
senescent
cells,
we
found
that
HERVK
(HML-2),
most
recently
integrated
ERVs,
are
unlocked
transcribe
genes
produce
retrovirus-like
particles
(RVLPs).
These
RVLPs
constitute
a
transmissible
message
elicit
senescence
phenotypes
young
which
be
blocked
by
neutralizing
antibodies.
The
activation
of
ERVs
was
also
observed
organs
aged
primates
mice
well
tissues
serum
from
elderly.
Their
repression
alleviates
cellular
tissue
degeneration
and,
some
extent,
organismal
aging.
findings
indicate
resurrection
hallmark
driving
force