PeerJ,
Journal Year:
2024,
Volume and Issue:
12, P. e18348 - e18348
Published: Oct. 24, 2024
tRNA-derived
small
RNAs
(tsRNAs)
are
a
novel
class
of
noncoding
RNAs,
precisely
cleaved
from
tRNA,
functioning
as
regulatory
molecules.
The
topic
tsRNAs
in
injuries
has
not
been
extensively
discussed,
and
studies
on
entering
new
era.
Here,
we
provide
fresh
perspective
this
topic.
We
systematically
reviewed
the
classification,
generation,
biological
functions
response
to
stress,
well
their
potential
biomarkers
therapeutic
targets
various
injuries,
including
lung
injury,
liver
renal
cardiac
neuronal
vascular
skeletal
muscle
skin
injury.
also
provided
association
between
stress-induced
organ
injury
clinical
perspective.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(24)
Published: April 19, 2024
Abstract
Preventing
and
treating
avascular
necrosis
at
the
distal
end
of
flaps
are
critical
to
surgery
success,
but
current
treatments
not
ideal.
A
recent
study
shows
that
apoptotic
bodies
(ABs)
generated
near
site
apoptosis
can
be
taken
up
promote
cell
proliferation.
The
reveals
ABs
derived
from
fibroblast‐like
cells
in
subcutaneous
connective
tissue
(FSCT
cells)
skin
promoted
ischaemic
flap
survival.
It
is
also
found
inhibited
death
oxidative
stress
M1‐to‐M2
polarization
macrophages.
Transcriptome
sequencing
protein
level
testing
demonstrated
survival
endothelial
macrophages
by
inhibiting
ferroptosis
via
KEAP1‐Nrf2
axis.
Furthermore,
microRNA
(miR)
data
vitro
vivo
experiments
KEAP1
delivering
miR‐339‐5p
exert
therapeutic
effects.
In
conclusion,
FSCT
cell‐derived
ferroptosis,
macrophage
transition
miR‐339‐5p/KEAP1/Nrf2
axis
These
results
provide
a
potential
strategy
administering
ABs.
MedComm,
Journal Year:
2024,
Volume and Issue:
5(10)
Published: Sept. 20, 2024
Radiation-induced
tissue
injury
(RITI)
is
the
most
common
complication
in
clinical
tumor
radiotherapy.
Due
to
heterogeneity
response
of
different
tissues
radiation
(IR),
radiotherapy
will
cause
types
and
degrees
RITI,
which
greatly
limits
application
Efforts
are
continuously
ongoing
elucidate
molecular
mechanism
RITI
develop
corresponding
prevention
treatment
drugs
for
RITI.
Single-cell
sequencing
(Sc-seq)
has
emerged
as
a
powerful
tool
uncovering
mechanisms
identifying
potential
targets
by
enhancing
our
understanding
complex
intercellular
relationships,
facilitating
identification
novel
cell
phenotypes,
allowing
assessment
spatiotemporal
developmental
trajectories.
Based
on
comprehensive
review
we
analyzed
regulatory
networks
combination
with
Sc-seq
summarized
targeted
intervention
pathways
therapeutic
Deciphering
diverse
underlying
can
shed
light
its
pathogenesis
unveil
new
avenues
potentially
facilitate
repair
or
regeneration
currently
irreversible
Furthermore,
discuss
how
personalized
strategies
based
offer
promise
mitigating
Small,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 28, 2025
Abstract
The
induction
of
apoptosis
in
tumor
cells
is
a
common
target
for
the
development
anti‐tumor
therapies;
however,
these
therapies
still
leave
patients
at
increased
risk
disease
recurrence.
For
example,
apoptotic
can
promote
growth
and
immune
evasion
via
secretion
metabolites,
extracellular
vesicles,
pro‐tumorigenic
macrophages.
This
paradox
effects
cell
has
begged
question
whether
suitable
cancer
therapy,
led
to
further
explorations
into
other
immunogenic
death‐based
approaches.
However,
strategies
face
multiple
challenges,
most
critical
which
microenvironment.
Contrary
promotion
tolerance
mediated
by
cells,
bodies
with
enriched
tumor‐related
antigens
have
demonstrated
great
potential,
as
evidenced
their
ability
initiate
systemic
T‐cell
responses.
These
characteristics
indicate
that
body‐based
could
be
ideal
“in
situ”
extra‐tumoral
vaccine
candidates
treatment
cancers,
address
current
issues
apoptosis‐based
or
immunotherapy
treatments.
Although
not
yet
tested
clinically,
vaccines
potential
better
patient
outcomes
future.
Shock,
Journal Year:
2024,
Volume and Issue:
62(4), P. 556 - 564
Published: July 16, 2024
ABSTRACT
Both
abdominal
radiotherapy
and
a
nuclear
event
can
result
in
gastrointestinal
symptoms,
including
acute
radiation
syndrome
(GI-ARS).
GI-ARS
is
characterized
by
compromised
intestinal
barrier
integrity
increasing
the
risk
for
infectious
complications.
Physiologically
relevant
animal
models
are
crucial
elucidating
host
responses
therapeutic
targets.
We
aimed
to
determine
dose
requirements
creating
Sinclair
minipig.
Male,
sexually
mature
swine
were
randomly
divided
into
sham
(n
=
6)
three
lower
hemibody
dosage
groups
of
8,
10,
12
Gy
5/group)
delivered
using
linear
accelerator-derived
x-rays
(1.9
Gy/min).
Animals
monitored
symptoms
14
days
with
rectal
swab
blood
collection
at
0–3,
7,
followed
necropsy
western
blotting
histology.
Dose-dependent
increases
weight
loss,
diarrhea
severity,
mortality
(log-rank
test,
P
0.041)
seen.
Villi
length
was
significantly
reduced
all
irradiated
animals
compared
controls
(
<
0.001).
Serum
citrulline
decreased
bacterial
translocation
increased
after
irradiation
controls.
Increased
NLRP3
levels
post-mortem
jejunum
seen
0.0043)
as
well
IL-1β
group
0.041).
Radiation
survival
associated
significant
gut
microbial
community
shifts
beta
diversity.
Moreover,
decedents
had
Porphyromonas,
Campylobacter,
Bacteroides
,
Parvimonas
Fusobacterium
Aerococcus,
Lactobacillus,
Prevotella,
Streptococcus
.
Our
novel
minipig
model
showed
dose-dependent
clinical
GI-ARS.
These
findings
provide
invaluable
insights
intricate
interplay
between
GI-ARS,
inflammation,
microbiota
alterations
offering
potential
targets
diagnostic
interventions
exposure.
Immunological Reviews,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 19, 2024
Summary
Radiation,
a
universal
component
of
Earth's
environment,
is
categorized
into
non‐ionizing
and
ionizing
forms.
While
radiation
relatively
harmless,
possesses
sufficient
energy
to
ionize
atoms
disrupt
DNA,
leading
cell
damage,
mutation,
cancer,
death.
The
extensive
use
radionuclides
in
nuclear
technology
medical
applications
has
sparked
global
concern
for
their
capacity
cause
acute
chronic
illnesses.
Ionizing
induces
DNA
damage
either
directly
through
strand
breaks
base
change
or
indirectly
by
generating
reactive
oxygen
species
(ROS)
nitrogen
(RNS)
via
radiolysis
water.
This
triggers
complex
cellular
response
involving
recognition
cycle
arrest,
repair
mechanisms,
release
pro‐inflammatory
cytokines,
review
focuses
on
the
mechanisms
radiation‐induced
subsequent
activation
processes,
critical
role
innate
immune
resolution
injury.
Emphasis
placed
pattern
receptors
(PRRs)
related
that
detect
damage‐associated
molecular
patterns
(DAMPs)
initiate
downstream
signaling
pathways.
Radiation‐induced
death
pathways
are
discussed
detail.
Understanding
these
processes
crucial
developing
strategies
mitigate
harmful
effects
improve
therapeutic
outcomes.
Cancer Medicine,
Journal Year:
2024,
Volume and Issue:
13(21)
Published: Nov. 1, 2024
ABSTRACT
Background
Radiotherapy
plays
a
fundamental
role
in
the
treatment
of
patients
with
all
stages
non‐small‐cell
lung
cancer
(NSCLC).
The
emergence
immune
checkpoint
inhibitors
(ICIs)
has
transformed
standard
care
these
patients.
use
ICIs
is
increasingly
utilized
definitive
setting
as
an
adjunct
to
chemoradiotherapy
or
surgery
and
remains
vital
component
metastatic
disease.
Despite
improvements
patient
survival,
immunotherapy
monotherapy
shown
limited
overall
response
rates
susceptibility
resistance.
been
identified
viable
option
enhance
rate
ICI
improve
outcomes
NSCLC.
Methods
We
queried
English
PubMed
database
utilizing
variably
combined
search
items
including
“radiation,”
“chemoradiation,”
“immune
checkpoint,”
“immunotherapy,”
“stereotactic
body
radiotherapy,”
“non‐small‐cell
lung”.
additionally
searched
various
acceptable
alternative
terms
for
similar
keywords
such
“radiotherapy”
place
“radiation.”
These
results
were
subsequently
curated
relevance
impact
on
current
paradigms.
Results
In
this
review,
we
discuss
preclinical
clinical
studies
relating
combinatorial
radiation
are
presented
context
early‐stage,
operable
stage
III,
unresectable
majority
data
illustrate
promising
regarding
additive
synergistic
effects
suggestion
that
timing
modalities
crucial
optimizing
outcomes.
Conclusion
While
there
now
evidence
favorable
interplay
between
NSCLC,
remain
multiple
unanswered
questions
which
expected
be
addressed
ongoing
trials.
Journal of Leukocyte Biology,
Journal Year:
2024,
Volume and Issue:
116(5), P. 1072 - 1079
Published: June 26, 2024
Abstract
Macrophages
are
essential
immune
cells
for
host
defense
against
bacterial
pathogens
after
radiation
injury.
However,
the
role
of
macrophage
phagocytosis
in
infection
following
injury
remains
poorly
examined.
Extracellular
cold-inducible
RNA-binding
protein
is
a
damage-associated
molecular
pattern
that
dysregulates
system
responses
such
as
phagocytosis.
We
hypothesized
radiation-induced
extracellular
release
impairs
bacteria.
Adult
healthy
mice
were
exposed
to
6.5
Gy
total
body
irradiation.
Primary
peritoneal
macrophages
isolated
from
adult
radiation.
protein–neutralizing
monoclonal
antibody
was
added
cell
culture
prior
Bacterial
by
assessed
using
pHrodo
Green-labeled
Escherichia
coli
7
d
irradiation
ex
vivo
and
vitro.
also
treatment
with
recombinant
murine
protein.
Rac1
ARP2
expression
lysates
levels
lavage
western
blotting.
significantly
decreased
compared
controls
downregulated
Total
increased
cavity.
Recombinant
dose-dependent
manner.
restored
Ionizing
exposure
Neutralization
restores
phagocytic
ability
Our
findings
elucidate
novel
mechanism
dysfunction
provide
potential
new
therapeutic
approach
limiting