DNA-methylation
clocks
inform
not
only
about
chronological
but
also
biological
age,
which
brings
a
high
resolution
and
precise
understanding
of
age-related
pathology
physiology.
Attempts
based
on
transcriptomic
epigenetic
approaches
arise
as
integrative
biomarkers
linking
the
quantification
stress
response
with
given
fitness
trait
may
help
to
identify
age
markers,
considered
welfare
indicators.
In
gilthead
sea
bream,
targeted
gene
expression
analyses
in
white
skeletal
muscle
proved
sirt1
reliable
marker
age-mediated
changes
energy
metabolism.
To
complete
list
auditing
biomarkers,
wide-analyses
one-
three-year
old
fish
were
combined.
After
discriminant
analysis,
668
differentially
expressed
transcripts
matched
those
containing
methylated
(DM)
regions
(14,366),
172
overlapping.
Through
enrichment
selection,
two
sets
genes
retained:
33
showing
an
opposite
trend
for
expression,
57
down-regulated
hypo-methylated.
The
first
set
displayed
apparently
more
reproducible
pattern
10
multifunctional
DM
CpG
regulatory
(sirt1,
smad1,
ramp1,
psmd2
–
up-regulated;
col5a1,
calcrl,
bmp1,
thrb,
spred2,
atp1a2
down-regulated)
deemed
candidate
markers
improved
bream.
International Journal of Dermatology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
ABSTRACT
The
concept
of
aging
has
evolved
from
being
primarily
attributed
to
genetic
factors
recognizing
the
critical
role
epigenetic
mechanisms.
Recent
advancements,
such
as
clocks,
have
provided
tools
assess
biological
age
and
offer
insights
into
processes
at
molecular
level.
In
aesthetic
dermatology,
understanding
these
allows
for
more
personalized,
effective
interventions
targeting
root
causes
skin
aging.
This
review
explores
interplay
changes,
aging,
potential
personalized
care
enhance
longevity
rejuvenation.
is
based
on
an
extensive
literature
search
conducted
across
PubMed
other
scientific
databases.
Studies
focused
mechanisms
DNA
methylation,
histone
modifications,
their
relationship
Particular
attention
was
given
recent
advancements
in
including
Horvath's
Clock
GrimAge,
implications
dermatological
treatments.
Epigenetic
Clock,
demonstrated
utility
assessing
through
methylation
markers,
revealing
actionable
processes.
Energy‐based
devices
like
fractional
lasers
radiofrequency
shown
promise
reversing
age‐related
promoting
collagen
synthesis,
reducing
age.
Additionally,
lifestyle
diet,
sleep,
circadian
rhythm
alignment
significantly
influence
health.
Integrating
dermatology
represents
a
paradigm
shift
rejuvenation,
allowing
treatments
that
address
visible
signs
underlying
Using
clocks
provides
framework
tailoring
individual
patient
needs,
optimizing
outcomes,
extending
results.
Future
research
should
focus
longitudinal
studies,
accessibility,
ethical
considerations
fully
harness
epigenetics
health
overall
well‐being.
Morphology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 11, 2025
Cellular
senescence
is
currently
one
of
the
dominant
concepts
aging.
Some
cells
in
developing
tissues
(prenatal
histogenesis)
and
definitive
acquire
morphofunctional
changes
associated
with
an
increase
size,
formation
special
areas
heterochromatin,
a
secretory
phenotype
production
proinflammatory
cytokines,
β-galactosidase,
TGFβ,
etc.
combination
blocking
mitosis
due
to
active
transcription
р16INK4A,
p21CIP1.
It
assumed
that
such
cells,
called
senescent,
are
not
transitional
form
histogenesis
from
actively
functioning
component
differon
dying
by
programmed
types
cell
death,
but
separate
functional
stage
cytogenesis.
The
histogenetic
significance
physiological
reparative
regeneration
various
tissues,
as
well
their
effect
on
histophysiology,
requires
further
study.
Pharmacological
elimination
senescent
section
anti-aging
therapy.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 15, 2024
Abstract
Nucleosome
remodeling
complexes
and
other
regulatory
factors
work
in
concert
to
build
a
chromatin
environment
that
directs
the
expression
of
distinct
set
genes
each
cell
using
cis-regulatory
elements
(CREs),
such
as
promoters
enhancers,
drive
transcription
both
mRNAs
CRE-associated
non-coding
RNAs
(ncRNAs).
Two
classes
ncRNAs
include
upstream
antisense
(uaRNAs),
which
are
transcribed
divergently
from
shared
mRNA
promoter,
enhancer
(eRNAs),
bidirectionally
active
enhancers.
The
complicated
network
CRE
regulation
by
nucleosome
remodelers
remains
only
partially
explored,
with
focus
on
select,
limited
number
remodelers.
We
endeavored
elucidate
remodeler-based
governing
(mRNA,
eRNA,
uaRNA)
murine
embryonic
stem
(ES)
cells
test
hypothesis
many
SNF2-family
collaborate
regulate
coding
transcriptome
via
alteration
underlying
architecture.
Using
depletion
followed
transient
sequencing
(TT-seq),
we
identified
thousands
misregulated
across
examined,
identifying
novel
contributions
understudied
transcription.
Our
findings
suggest
eRNA
coordinately
co-regulated,
while
uaRNAs
sharing
common
promoter
independently
regulated.
Subsequent
mechanistic
studies
SRCAP
CHD8
modulate
through
classical
mechanisms
histone
variants,
broad
including
SMARCAL1
indirectly
contribute
transcriptional
maintenance
genomic
stability
proper
Integrator
complex
localization.
This
study
systematically
examines
contribution
SNF2-remodelers
transcriptome,
at
least
two
for
remodeler
action.
Ecotoxicology and Environmental Safety,
Journal Year:
2024,
Volume and Issue:
287, P. 117284 - 117284
Published: Nov. 1, 2024
The
increasing
environmental
presence
of
nanoplastics
(NPs)
has
raised
concerns
about
their
potential
impact
on
biological
systems.
We
investigated
the
repercussions
polymethyl
methacrylate
(PMMA)
NPs
exposure
normal
gastric
epithelial
cells
and
revealed
a
pronounced
increase
in
senescence-associated
β-galactosidase
activity
G1
phase
cell
cycle
arrest.
Our
study
demonstrated
dose-dependent
reactive
oxygen
species
(ROS)
DNA
damage,
underscoring
pivotal
role
ROS
PMMA
NPs-mediated
effects,
novel
contribution
to
existing
body
knowledge
dominated
by
polystyrene
particles.
Furthermore,
we
explored
influence
damage
response
mechanisms,
highlighting
significant
inhibition
nonhomologous
end-joining
(NHEJ).
findings
help
elucidate
consequent
genomic
instability,
as
evidenced
increased
chromosomal
aberrations
micronuclei
formation.
By
connecting
these
cellular
manifestations
organism-level
hypothesize
that
play
critical
aging
processes.
work
an
activated
cGAS-STING
signaling
pathway
after
exposure,
which
correlated
with
aging-related
inflammation
behavioral
changes
mice.
Importantly,
our
provides
comprehensive
evidence
NPs-induced
premature
cells,
shedding
light
molecular
intricacies
underlying
repair
impairment,
inflammation.
research
prompts
heightened
caution
regarding
risks
calls
for
further
investigation
into
broader
implications
pollutants
processes
higher
organisms.
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(11), P. 2540 - 2540
Published: Nov. 7, 2024
The
impressive
achievements
made
in
the
last
century
extending
lifespan
have
led
to
a
significant
growth
rate
of
elderly
individuals
populations
across
world
and
an
exponential
increase
incidence
age-related
conditions
such
as
cardiovascular
diseases,
diabetes
mellitus
type
2,
neurodegenerative
diseases.
To
date,
geroscientists
identified
12
hallmarks
aging
(genomic
instability,
telomere
attrition,
epigenetic
alterations,
loss
proteostasis,
impaired
macroautophagy,
mitochondrial
dysfunction,
nutrient
sensing,
cellular
senescence,
stem
cell
exhaustion,
defective
intercellular
communication,
chronic
inflammation,
gut
dysbiosis),
intricately
linked
among
each
other,
which
can
be
targeted
with
senolytic
or
senomorphic
drugs,
well
more
aggressive
approaches
cell-based
therapies.
side
effects
seriously
limit
use
these
drugs.
However,
since
rejuvenation
is
dream
mankind,
future
research
expected
improve
tolerability
available
drugs
highlight
novel
strategies.
In
meantime,
medical
community,
healthcare
providers,
society
should
decide
when
start
treatments
how
tailor
them
individually.
Egyptian Liver Journal,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: Nov. 12, 2024
Abstract
Background
Polyploidization,
a
process
where
cells
acquire
additional
chromosome
sets,
is
unique
characteristic
of
hepatocytes.
This
has
been
increasingly
recognized
as
an
adaptive
mechanism
for
maintaining
liver
function
during
aging,
period
characterized
by
cellular
senescence,
DNA
damage,
and
metabolic
dysregulation.
Purpose
review
explores
the
molecular
mechanisms
underlying
hepatocyte
polyploidization
its
potential
role
in
promoting
resilience
against
aging-related
decline
function.
We
assess
how
polyploid
hepatocytes
contribute
to
genomic
stability,
stress
resistance,
adaptation,
highlighting
their
relevance
aging.
Main
body
Hepatocyte
occurs
through
such
cytokinesis
failure
endoreplication,
leading
binuclear
or
mononuclear
cells.
Polyploid
exhibit
enhanced
repair
capacity,
which
helps
mitigate
accumulation
age-related
damage.
The
increased
gene
dosage
facilitates
better
responses,
particularly
oxidative
genotoxic
insults.
Metabolic
adaptations,
including
xenobiotic
metabolism
lipid
regulation,
further
support
liver’s
ability
maintain
homeostasis
Additionally,
demonstrate
altered
epigenetic
landscapes
proteostasis
mechanisms,
contributing
improved
reduced
susceptibility
senescence.
These
adaptations
collectively
enhance
structural
challenges.
Conclusion
represents
critical
protective
that
safeguard
instability,
dysfunction,
stress.
Understanding
pathways
driving
could
pave
way
novel
therapeutic
strategies
combat
disorders
health
span.
Graphical
Aging advances.,
Journal Year:
2024,
Volume and Issue:
1(2), P. 118 - 134
Published: Dec. 1, 2024
Aging
is
a
complex
biological
process
characterized
by
gradual
deterioration
in
physiological
activities,
contributing
to
an
elevated
risk
of
different
age-associated
malignancies,
including
cancer.
The
current
review
paper
aims
elucidate
the
association
between
hallmarks
aging
and
parallel
development
Various
cellular
molecular
mechanisms
underlying
such
as
senescence,
genomic
instability,
telomere
shortening
play
significant
role
accumulation
genetic
mutations
disruption
activities.
It
has
also
discussed
immune
system’s
aging,
indicating
how
age-linked
dysfunction
compromises
body’s
capacity
recognize
eradicate
pre-tumorous
cells,
thus
promoting
cancer
advancement.
This
examines
affects
tumor
microenvironment,
where
age-related
alterations
stromal
extracellular
matrix
factors
lead
conditions
that
promote
growth
proliferation.
Furthermore,
it
discusses
concept
“accelerated
aging”
survivors,
highlighting
negative
effects
its
therapy
intensify
process,
resulting
greater
physical
cognitive
decline.
explores
prospect
new
therapies
target
aging-related
processes
ameliorate
outcomes.
Overall,
underscores
need
for
ongoing
interdisciplinary
research
understand
relationship
cancer,
ultimately
aiming
develop
more
effective
prevention
treatment
approaches.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(7), P. 4113 - 4113
Published: April 8, 2024
Precision
oncology
is
based
on
deep
knowledge
of
the
molecular
profile
tumors,
allowing
for
more
accurate
and
personalized
therapy
specific
groups
patients
who
are
different
in
disease
susceptibility
as
well
treatment
response.
Thus,
onco-breastomics
able
to
discover
novel
biomarkers
that
have
been
found
racial
ethnic
differences,
among
other
types
disparities
such
chronological
or
biological
age-,
sex/gender-
environmental-related
ones.
Usually,
evidence
suggests
breast
cancer
(BC)
due
ethnicity,
aging
rate,
socioeconomic
position,
environmental
chemical
exposures,
psycho-social
stressors,
comorbidities,
Western
lifestyle,
poverty
rurality,
organizational
health
care
system
factors
access.
The
aim
this
review
was
deepen
understanding
BC-related
disparities,
mainly
from
a
biomedical
perspective,
which
includes
genomic-based
tumor
biology
developmental
biology,
differences
tumors'
immune
metabolic
landscapes,
ecological
involved
these
microbiomics-
metagenomics-based
BC.
We
can
conclude
onco-breastomics,
principle,
genomics,
proteomics,
epigenomics,
hormonomics,
metabolomics
exposomics
data,
characterize
multiple
processes
pathways
BC
clarifying
incidence,
mortality
response
patients.
Nutrients,
Journal Year:
2024,
Volume and Issue:
16(17), P. 2835 - 2835
Published: Aug. 24, 2024
Aging
is
the
result
of
accumulation
a
wide
variety
molecular
and
cellular
damages
over
time,
meaning
that
“the
more
damage
we
accumulate,
higher
possibility
to
develop
age-related
diseases”.
Therefore,
reduce
incidence
such
diseases
improve
human
health,
it
becomes
important
find
ways
combat
damage.
In
this
sense,
geroprotectors
have
been
suggested
as
molecules
could
slow
down
or
prevent
diseases.
On
other
hand,
nutraceuticals
are
another
set
compounds
align
with
need
promote
health
since
they
biologically
active
(occurring
naturally
in
food)
that,
apart
from
having
nutritional
role,
preventive
properties,
antioxidant,
anti-inflammatory
antitumoral,
just
mention
few.
present
review
using
specialized
databases
Scopus
PubMed
collected
information
articles
published
2010
2023
order
describe
role
during
aging
process
and,
given
their
targeting
hallmarks
aging,
suggest
potential
be
consumed
part
our
regular
diet
administered
additionally
supplements.