International Immunopharmacology,
Journal Year:
2024,
Volume and Issue:
138, P. 112553 - 112553
Published: June 28, 2024
Lung
adenocarcinoma
(LUAD)
is
the
most
common
and
aggressive
cancer
with
a
high
incidence.
N1-specific
pseudouridine
methyltransferase
(EMG1),
highly
conserved
nucleolus
protein,
plays
an
important
role
in
biological
development
of
ribosomes.
However,
EMG1
progression
LUAD
still
unclear.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Feb. 28, 2024
Background
Cervical
carcinoma
(CC)
represents
a
prevalent
gynecological
neoplasm,
with
discernible
rise
in
prevalence
among
younger
cohorts
observed
recent
years.
Nonetheless,
the
intrinsic
cellular
heterogeneity
of
CC
remains
inadequately
investigated.
Methods
We
utilized
single-cell
RNA
sequencing
(scRNA-seq)
transcriptomic
analysis
to
scrutinize
tumor
epithelial
cells
derived
from
four
specimens
cervical
patients.
This
method
enabled
identification
pivotal
subpopulations
and
elucidation
their
contributions
progression.
Subsequently,
we
assessed
influence
associated
molecules
bulk
(Bulk
RNA-seq)
performed
experiments
for
validation
purposes.
Results
Through
our
analysis,
have
discerned
C3
PLP2+
Tumor
Epithelial
Progenitor
Cells
as
noteworthy
subpopulation
(CC),
exerting
on
differentiation
progression
CC.
established
an
independent
prognostic
indicator—the
EPCs
score.
By
stratifying
patients
into
high
low
score
groups
based
median
score,
that
high-score
group
exhibits
diminished
survival
rates
compared
low-score
group.
The
correlations
between
these
immune
infiltration,
enriched
pathways,
single-nucleotide
polymorphisms
(SNPs),
drug
sensitivity,
other
factors,
further
underscore
impact
prognosis.
Cellular
validated
significant
ATF6
proliferation
migration
cell
lines.
Conclusion
study
enriches
comprehension
determinants
shaping
CC,
elevates
cognizance
microenvironment
offers
valuable
insights
prospective
therapies.
These
discoveries
contribute
refinement
diagnostics
formulation
optimal
therapeutic
approaches.
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(5), P. e26604 - e26604
Published: Feb. 24, 2024
BackgroundColorectal
cancer
(CRC)
is
the
third
most
prevalent
tumor
globally.
The
liver
common
site
for
CRC
metastasis,
and
involvement
of
a
cause
death
in
patients
with
late-stage
CRC.
Consequently,
mitigating
metastasis
(CRLM)
key
to
improving
prognosis
increasing
survival.
Exercise
has
been
shown
be
an
effective
method
many
types.
However,
ability
exercise
inhibit
CRLM
yet
thoroughly
investigated.MethodsThe
GSE157600
GSE97084
datasets
were
used
analysis.
A
pan-cancer
dataset
which
was
uniformly
normalized
downloaded
analyzed
from
UCSC
database:
TCGA,
TARGET,
GTEx
(PANCAN,
n
=
19,131,
G
60,499).
Several
advanced
bioinformatics
analyses
conducted,
including
single-cell
sequencing
analysis,
correlation
algorithm,
prognostic
screen.
microarray
(TMA)
as
well
cell/animal
experiments
are
further
validate
results
analysis.ResultsThe
greatest
variability
found
epithelial
cells
group.
RPS4X
generally
upregulated
all
types
CRC,
while
downregulated
expression.
lowered
expression
may
prolong
survival
reduce
metastasis.
stemness
marker-CD44
highly
positively
correlated
knockdown
reduced
both
vitro
vivo.ConclusionRPS4X
upregulation
enhance
increase
odds
through
regulation
RPS4X.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: Aug. 24, 2023
Lung
cancer
constitutes
a
formidable
menace
to
global
health
and
well-being,
as
its
incidence
mortality
rate
escalate
at
an
alarming
pace.
In
recent
years,
research
has
indicated
that
exercise
potential
roles
in
both
the
prevention
treatment
of
lung
cancer.
However,
exact
mechanism
coordinating
effect
on
is
unclear,
limiting
use
clinical
practice.
The
purpose
this
review
explore
mechanisms
through
which
exerts
anticancer
effects
against
This
will
analyze
biological
basis
exercise’s
cancer,
with
focus
aspects
such
tumor
microenvironment,
matrix
regulation,
apoptosis
angiogenesis.
Finally,
we
discuss
future
directions
applications.
BMB Reports,
Journal Year:
2023,
Volume and Issue:
56(7), P. 365 - 373
Published: June 1, 2023
Loss
of
skeletal
muscle
mass
is
a
primary
feature
sarcopenia
and
cancer
cachexia.
In
patients,
tumor-derived
inflammatory
factors
promote
atrophy
via
tumor-to-muscle
effects,
which
closely
associated
with
poor
prognosis.
During
the
past
decade,
has
been
considered
to
function
as
an
autocrine,
paracrine,
endocrine
organ
by
releasing
numerous
myokines.
The
circulating
myokines
can
modulate
pathophysiology
in
other
organs,
well
tumor
microenvironment,
suggesting
muscleto-tumor
signaling
molecules.
Here,
we
highlight
roles
tumorigenesis,
particularly
terms
crosstalk
between
tumor.
Better
understanding
muscle-to-tumor
effects
will
shed
light
on
novel
strategies
for
diagnosis
treatment
cancer.
[BMB
Reports
2023;
56(7):
365-373].
Frontiers in Genetics,
Journal Year:
2023,
Volume and Issue:
13
Published: Jan. 9, 2023
Head
and
neck
squamous
cell
carcinoma
(HNSCC),
the
most
common
malignancy
of
head
neck,
has
an
overall
5-year
survival
rate
<50%.
Genes
associated
with
cuproptosis,
a
newly
identified
copper-dependent
form
death,
are
aberrantly
expressed
in
various
tumours.
However,
their
role
HNSCC
remains
unknown.
In
this
study,
bioinformatic
analysis
revealed
that
cuproptosis-related
gene
CDKN2A
was
correlated
malignant
behaviour
HNSCC.
Kaplan-Meier
(KM)
curves
showed
patients
high
expression
had
better
prognosis.
Multiomic
may
be
cycle
immune
infiltration
tumour
microenvironment
is
important
for
maintaining
systemic
homeostasis
body.
Furthermore,
molecular
docking
dynamics
simulations
suggested
strong
binding
between
plicamycin
CDKN2A.
And
inhibits
progression
cellular
assays.
conclusion,
study
elucidated
potential
mechanism
action
cuproptosis-associated
targets
to
improve
prognosis
patients.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: July 31, 2024
Breast
cancer
ranks
as
one
of
the
most
prevalent
malignancies
among
women
globally,
with
increasing
incidence
rates.
Physical
activity,
particularly
exercise,
has
emerged
a
potentially
significant
modifier
prognosis,
influencing
tumor
biology
and
patient
outcomes.
Military Medical Research,
Journal Year:
2024,
Volume and Issue:
11(1)
Published: Jan. 2, 2024
Abstract
Background
One-third
of
veterans
returning
from
the
1990–1991
Gulf
War
reported
a
myriad
symptoms
including
cognitive
dysfunction,
skin
rashes,
musculoskeletal
discomfort,
and
fatigue.
This
symptom
cluster
is
now
referred
to
as
Illness
(GWI).
As
underlying
mechanisms
GWI
have
yet
be
fully
elucidated,
diagnosis
treatment
are
based
on
symptomatic
presentation.
One
confounding
factor
tied
illness
high
presence
post-traumatic
stress
disorder
(PTSD).
Previous
research
efforts
demonstrated
that
both
PTSD
associated
with
immunological
dysfunction.
such,
this
endeavor
aimed
provide
insight
into
complex
relationship
between
symptoms,
cytokine
presence,
immune
cell
populations
pinpoint
impact
these
measures
in
GWI.
Methods
Symptom
were
gathered
through
Multidimensional
fatigue
inventory
(MFI)
36-item
short
form
health
survey
(SF-36)
scales
biological
obtained
&
cytometry
analysis.
Subgrouping
was
conducted
using
Davidson
Trauma
Scale
scores
Structured
Clinical
Interview
for
Diagnostic
statistical
manual
mental
disorders
(DSM)-5,
probability
(GWI
H
)
low
L
).
Data
analyzed
Analysis
variance
(ANOVA)
analysis
along
correlation
graph
We
mapped
correlations
cells
signaling
measures,
hormones
identify
patterns
regulation
,
healthy
control
groups.
Results
comorbid
resulted
poorer
outcomes
compared
Healthy
(HC)
subgroup.
Significant
differences
found
basophil
levels
HC
at
peak
exercise
regardless
comorbidity
(ANOVA
F
=
4.7,
P
0.01,)
indicating
its
potential
usage
biomarker
general
control.
While
unique
identification
less
clear,
subgroup
delineated
IL-15
across
an
challenge
>
3.75,
<
0.03).
Additional
natural
killer
(NK)
numbers
function
highlight
absence
symptoms.
Conclusion
conclude
disentangling
by
defining
trauma-based
subgroups
may
aid
biosignatures
can
help
improve
target
more
effectively.
Cancer Medicine,
Journal Year:
2024,
Volume and Issue:
13(3)
Published: Jan. 17, 2024
Abstract
Background
Mammary
carcinoma,
a
pervasive
and
potentially
lethal
affliction,
is
conjectured
to
be
profoundly
influenced
by
physical
exercise,
both
in
prophylaxis
therapeutic
contexts.
This
study
endeavors
explore
the
repercussions
of
exercise
training
on
progression
mammary
particularly
mechanisms
which
amalgamation
an
regimen
doxorubicin
induces
tumor
cell
apoptosis.
Methods
Female
BALB/c
mice
were
categorized
into
four
distinct
groups:
A
sedentary
group
(SED),
(Ex),
(Dox,
5
mg/kg),
combined
treatment
(Dox
+
Ex).
The
lasted
for
21
days
included
aerobic
rotarod
resistance
training.
impact
growth,
immune
proportions,
inflammatory
factor
levels,
apoptosis
pathway
was
assessed.
Results
Exercise
significantly
curtailed
growth
mouse
model
breast
cancer.
Both
Ex
Dox
groups
exhibited
significant
reductions
volume
weight
(
p
<
0.01)
comparison
SED
group,
while
had
lower
than
0.01).
also
increased
proportion
NK
T
cells
various
parts
body
tissue,
decreasing
blood
vessels
density.
IL‐6
IL‐15
levels
altered
expression
apoptosis‐related
proteins
with
showing
even
more
changes.
Conclusions
Physical
improves
effectiveness
treating
cancer
activating
cytotoxic
cells,
releasing
suppressor
factors,
initiating
mt‐apoptosis,
all
mitigating
adverse
effects
chemotherapy.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Aug. 5, 2024
Breast
cancer,
one
of
the
most
prevalent
malignancies
among
women
worldwide,
has
rising
incidence
rates.
Physical
activity,
particularly
exercise,
emerged
as
a
significant
modifier
cancer
prognosis,
influencing
both
tumor
biology
and
patient
outcomes.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Jan. 22, 2025
Bladder
cancer
is
one
of
the
most
common
malignancies
urinary
system
and
has
always
presented
great
challenges
in
treatment
due
to
its
intricate
biological
features
high
recurrence
rates.
Although
developments
were
achieved
immunotherapy
targeted
therapies
within
last
decade,
therapeutic
outcomes
for
a
number
patients
remain
unsatisfactory,
particularly
as
long-term
efficacy.
Review
discusses
molecular
mechanisms
developed
during
process
bladder
progression:
genetic
epigenetic
alterations,
dynamics
tumor
microenvironment
(TME),
dysregulation
abnormal
activation
various
signaling
pathways—all
contributing
resistance.
It
mutation,
especially
both
low-
high-grade
tumors,
that,
alongside
modifications,
plays
considerable
role
aggressiveness
drug
TME,
comprising
cancer-associated
fibroblasts
(CAFs),
immunosuppressive
cells,
different
components
extracellular
matrix
(ECM),
orchestrates
setting
that
fosters
growth
immune
evasion
confers
resistance
on
any
regime
might
be
used.
The
review
also
provides
an
overview
PI3K/AKT
MAPK
pathways
progression
development
against
them.
Further,
it
immunotherapy,
including
those
involving
checkpoint
inhibitors.
Other
promising
approaches
include
new
strategies
target
not
only
but
checkpoints
combination
therapies.
This
aims
contribute
elaboration
more
effective
personalized
by
fully
understanding
underlying
involved
cancer.