Alzheimer s & Dementia,
Journal Year:
2025,
Volume and Issue:
21(2)
Published: Feb. 1, 2025
Abstract
The
characteristic
events
in
neurodegenerative
diseases
(NDDs)
encompass
protein
misfolding,
aggregation,
accumulation,
and
their
related
cellular
dysfunction,
synaptic
function
loss.
While
distinct
proteins
are
implicated
the
pathological
processes
of
different
NDDs,
process
misfolding
aggregation
remains
notably
similar
across
various
conditions.
Specifically,
undergo
into
beta‐folded
(β‐folded)
conformation,
resulting
formation
insoluble
amyloid
proteins.
Despite
advancements
comprehending
certain
facets
this
intricate
remain
incompletely
elucidated.
In
recent
years,
concept
that
long
non‐coding
RNAs
(lncRNAs)
contribute
to
has
gained
recognition.
LncRNAs
influence
aggregates
by
facilitating
overexpression
through
regulation
gene
transcription
translation,
inhibiting
degradation
via
lysosomal
autophagic
pathways,
targeting
aberrant
modifications
phase
transitions
A
better
understanding
relationship
between
lncRNAs
is
an
important
step
dissecting
underlying
molecular
mechanisms
will
discovery
new
therapeutic
targets
strategies.
Highlights
NDDs
marked
leading
dysfunction
loss
function.
being
involved
β‐folded
conformations
forming
consistent
role
attention,
as
they
regulate
inhibit
degradation,
target
modifications.
Understanding
link
crucial
for
uncovering
developing
targets.
Drug Development Research,
Journal Year:
2025,
Volume and Issue:
86(1)
Published: Jan. 20, 2025
ABSTRACT
Chemotherapy
is
an
effective
treatment
for
gastric
cancer.
However,
many
patients
develop
resistance
to
chemotherapeutic
agents
during
clinical
treatment.
LncRNA
CCAT1
has
recently
been
shown
influence
cellular
specific
drugs,
but
its
role
in
cancer
remains
underexplored.
This
study
aims
investigate
the
of
cisplatin
cells
and
potential
underlying
mechanisms.
Gastric
cell
lines
with
acquired
were
established.
The
expression
was
assessed
both
cisplatin‐sensitive
cisplatin‐resistant
AGS
lines.
knocked
down
AGS/DDP
cells,
changes
IC50
values
measured
using
Cell
Counting
Kit‐8
(CCK‐8)
assay.
Apoptosis
evaluated
by
flow
cytometry.
Additionally,
Western
blotting
employed
measure
levels
PI3K/AKT/mTOR
signaling
pathway
proteins
apoptosis‐related
interference
control
groups.
RT‐qPCR
results
indicated
that
significantly
elevated
compared
non‐resistant
cells.
Similarly,
CCK‐8
assay
demonstrated
knocking
resistant
increased
their
sensitivity
Flow
cytometry
blot
further
confirmed
silencing
promoted
apoptosis
these
higher
sensitive
counterparts,
resulted
reduced
proteins.
In
conclusion,
above
studies
induced
Experimental Dermatology,
Journal Year:
2025,
Volume and Issue:
34(2)
Published: Feb. 1, 2025
ABSTRACT
Psoriasis
is
a
common
chronic
inflammatory
skin
disease
determined
by
genetic
and
environmental
factors,
resulting
in
the
activation
of
IL‐23/IL‐17‐mediated
immune
response,
epidermal
hyperproliferation,
keratinocyte
activation.
Long
non‐coding
RNAs
(lncRNAs)
are
non‐protein‐coding
transcripts
>
500
nucleotides
with
diverse
regulatory
functions;
their
role
dysfunction
psoriasis
poorly
understood.
To
identify
potential
roles
psoriasis,
including
lncRNAs,
we
performed
RNA
sequencing
on
keratinocytes
from
healthy
skin.
We
identified
889
differentially
expressed
many
which
yet
unknown
functions.
RP11‐295G20.2
was
as
lncRNA
significantly
induced
keratinocytes,
this
verified
qRT‐PCR
single‐molecule
situ
hybridisation.
Analysis
subcellular
fractions
epidermis
revealed
cytoplasmic
localisation
line
results
single
molecule
report
that
has
skin‐enriched
expression,
within
it
mainly
suprabasal
layers.
Moreover,
key
cytokine
IL‐17A
shows
dynamic
regulation
during
differentiation
upregulation
early
downregulation
late
stage.
Knockdown
promotes
terminal
differentiation.
Based
our
findings,
named
C
ytoplasmic
D
ifferentiation‐
A
ssociated
Epidermal
R
NA,
CYDAER.
In
summary,
study
provides
comprehensive
characterisation
landscape
identifies
CYDAER
regulating
Our
data
suggest
overexpression
may
contribute
to
altered
psoriatic
epidermis.
Small Methods,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 25, 2025
Abstract
Exosomes
have
emerged
as
versatile
biomolecules
in
gastrointestinal
(GI)
cancer
management,
leveraging
their
inherent
cargo‐carrying
capabilities
to
overcome
the
limitations
of
current
diagnostic
and
therapeutic
strategies.
This
review
provides
a
comprehensive
exploration
exosome‐based
technologies,
highlighting
dual
roles
biomarkers
vehicles.
On
front,
this
investigates
specific
exosomal
biomarkers—including
miRNAs,
lncRNAs,
circRNAs,
proteins—emphasizing
tumor
biology
clinical
utility,
such
accuracy,
early
detection
potential,
prognostic
significance.
Therapeutically,
study
examines
sources,
purification
methodologies,
engineering
strategies
that
enhance
efficacy
exosomes
modulating
immune
responses,
overcoming
drug
resistance,
suppressing
metastasis.
By
providing
overview
field,
serves
guideline
for
researchers
clinicians
entering
offering
novel
insights
into
potential
theranostic
systems
delineating
future
directions
existing
challenges.
Trends in Genetics,
Journal Year:
2022,
Volume and Issue:
39(2), P. 125 - 139
Published: Sept. 19, 2022
Mitochondria,
organelles
that
harbor
their
own
circular
genomes,
are
critical
for
energy
production
and
homeostasis
maintenance
in
eukaryotic
cells.
Recent
studies
discovered
hundreds
of
mitochondria-encoded
noncoding
RNAs
(mt-ncRNAs),
including
novel
subtypes
(mecciRNAs)
double-stranded
(mt-dsRNAs).
Here,
we
discuss
the
emerging
field
mt-ncRNAs
by
reviewing
expression
patterns,
biogenesis,
metabolism,
regulatory
roles,
functional
mechanisms.
Many
have
roles
cellular
physiology,
some
associated
with,
or
even
act
as,
causal
factors
human
diseases.
We
also
highlight
developments
technologies
methodologies
further
insights
into
future
perspectives
challenges
studying
these
RNAs,
as
well
potential
biomedical
applications.
Journal for ImmunoTherapy of Cancer,
Journal Year:
2023,
Volume and Issue:
11(5), P. e006230 - e006230
Published: May 1, 2023
Background
Tumor-associated
macrophages
(TAMs)
are
a
major
component
of
the
tumor
microenvironment
(TME)
and
exert
an
important
role
in
progression.
Due
to
heterogeneity
plasticity
TAMs,
modulating
polarization
states
TAMs
is
considered
as
potential
therapeutic
strategy
for
tumors.
Long
noncoding
RNAs
(lncRNAs)
have
been
implicated
various
physiological
pathological
processes,
yet
underlying
mechanism
on
how
lncRNAs
manipulate
still
unclear
remains
be
further
investigated.
Methods
Microarray
analyses
were
employed
characterize
lncRNA
profile
involved
THP-1-induced
M0,
M1
M2-like
macrophage.
Among
those
differentially
expressed
lncRNAs,
NR_109
was
studied,
its
function
macrophage
effects
condition
medium
or
mediated
by
proliferation,
metastasis
TME
remodeling
both
vitro
vivo.
Moreover,
we
revealed
interacted
with
far
upstream
element-binding
protein
1
(FUBP1)
regulate
stability
through
hindering
ubiquitination
modification
competitively
binding
JVT-1.
Finally,
examined
sections
patients
probe
correlation
among
expression
related
proteins,
showing
clinical
significance
NR_109.
Results
We
found
that
highly
macrophages.
Knockdown
impeded
IL-4
induced
significantly
reduced
activity
support
proliferation
cells
Mechanistically,
competed
JVT-1
bind
FUBP1
at
C-terminus
domain,
ubiquitin-mediated
degradation
FUBP1,
activated
c-Myc
transcription
thus
promoted
polarization.
Meanwhile,
factor,
could
promoter
enhance
Clinically,
high
CD163
+
from
tissues
positively
correlated
poor
stages
gastric
cancer
breast
cancer.
Conclusions
Our
work
first
time
exerted
crucial
regulating
phenotype-remodeling
via
NR_109/FUBP1/c-Myc
positive
feedback
loop.
Thus,
has
great
translational
potentials
diagnosis,
prognosis
immunotherapy
Aging,
Journal Year:
2023,
Volume and Issue:
unknown
Published: April 19, 2023
Aging
|
doi:10.18632/aging.204666.
Noah
Wechter,
Martina
Rossi,
Carlos
Anerillas,
Dimitrios
Tsitsipatis,
Yulan
Piao,
Jinshui
Fan,
Jennifer
L.
Martindale,
Supriyo
De,
Krystyna
Mazan-Mamczarz,
Myriam
Gorospe
Secondary
spinal
cord
injury
(SCI)
often
causes
the
aggravation
of
inflammatory
reaction
and
nerve
injury,
which
affects
recovery
motor
function.
Bone-marrow-derived
macrophages
(BMDMs)
were
recruited
to
injured
area
after
SCI,
M1
polarization
is
key
process
for
inducing
response
neuronal
apoptosis.
We
previously
showed
that
photobiomodulation
(PBM)
can
inhibit
phenotype
BMDMs
reduce
inflammation,
but
underlying
mechanisms
are
unclear.
The
purpose
this
study
explore
potential
target
mechanism
PBM
in
treating
SCI.Transcriptome
sequencing
bioinformatics
analysis
long
noncoding
RNA
taurine
upregulated
gene
1
(lncRNA
TUG1)
was
a
PBM.
expression
specific
lncRNA
TUG1
detected
by
qPCR,
immunofluorescence,
flow
cytometry,
western
blotting,
fluorescence
situ
hybridization,
luciferase
assay.
Basso
mouse
scale
(BMS)
gait
used
evaluate
function
mice.Results
may
be
PBM,
regulating
BMDMs,
response,
axial
growth
DRG.
Mechanistically,
competed
with
TLR3
binding
miR-1192
attenuated
inhibitory
effect
on
TLR3.
This
protected
from
degradation,
enabling
high
TLR3,
promoted
activation
downstream
NF-κB
signal
release
cytokines.
In
vivo,
treatment
could
TUG1,
cytokines
survival
SCI
mice.Our
clarified
TUG1/miR-1192/TLR3
axis
an
important
pathway
macrophage
provides
theoretical
support
its
clinical
application
patients
SCI.
Cancers,
Journal Year:
2023,
Volume and Issue:
15(16), P. 4160 - 4160
Published: Aug. 17, 2023
ANRIL
(Antisense
Noncoding
RNA
in
the
INK4
Locus),
a
long
non-coding
encoded
human
chromosome
9p21
region,
is
critical
factor
for
regulating
gene
expression
by
interacting
with
multiple
proteins
and
miRNAs.
It
has
been
found
to
play
important
roles
various
cellular
processes,
including
cell
cycle
control
proliferation.
Dysregulation
of
associated
several
diseases
like
cancers
cardiovascular
diseases,
instance.
Understanding
oncogenic
role
its
potential
as
diagnostic
prognostic
biomarker
cancer
crucial.
This
review
provides
insights
into
regulatory
mechanisms
significance
locus
cancer.