Frontiers in Immunology,
Год журнала:
2024,
Номер
15
Опубликована: Окт. 24, 2024
Recent
studies
have
underscored
the
biological
significance
of
RNA
modifications
in
tumorigenicity
and
progression.
However,
potential
roles
immune
regulation
formation
tumor
microenvironment
(TME)
head
neck
squamous
carcinoma
(HNSC)
remain
unclear.
Frontiers in Oncology,
Год журнала:
2025,
Номер
15
Опубликована: Апрель 7, 2025
Cancer
treatment
has
long
been
hindered
by
the
complexity
of
tumor
microenvironment
(TME)
and
mechanisms
that
tumors
employ
to
evade
immune
detection.
Recently,
combination
checkpoint
inhibitors
(ICIs)
anti-angiogenic
therapies
emerged
as
a
promising
approach
improve
cancer
outcomes.
This
review
delves
into
role
immunostimulatory
molecules
ICIs
in
enhancing
anti-tumor
immunity,
while
also
discussing
therapeutic
potential
strategies
cancer.
In
particular,
we
highlight
critical
endoplasmic
reticulum
(ER)
stress
angiogenesis.
Moreover,
explore
macrophage
reprogramming
bolster
with
focus
on
restoring
phagocytic
function,
modulating
hypoxic
environments,
targeting
cytokines
chemokines
shape
responses.
By
examining
underlying
combining
therapies,
recent
clinical
trials
discuss
biomarkers
guide
predict
efficacy.
Cell Communication and Signaling,
Год журнала:
2025,
Номер
23(1)
Опубликована: Апрель 29, 2025
Extracellular
vesicles
(EVs)
are
nanoscale
structures
involved
in
intercellular
communication
and
play
a
key
role
cancer
pathology.
Intrahepatic
cholangiocarcinoma
(ICC)
is
highly
invasive
malignancy
marked
by
abnormal
sialylated
glycosylation.
Analyzing
proteins
glycans
EVs
provides
insights
into
ICC
molecular
subtyping
mechanisms.
Optimizing
EV
isolation
methods
for
ICC-derived
enables
comprehensive
proteomic
glycomic
analysis.
We
systematically
evaluated
five
methods-Ultracentrifugation
(UC),
exoEasy,
Total
Exosome
Isolation
(TEI),
EVtrap,
ÄKTA-by
analyzing
the
biophysical
properties,
profiles,
of
EVs.
Subsequently,
we
applied
TMT-based
quantitative
proteome
light/heavy
methylamine
labeling
quantification
N-glycan
linkage
isomers
to
investigate
alterations
N-glycans
within
secreted
HuCCT1
HCCC-9810
cells
with
overexpressing
ST6
β‑galactoside
α2,6‑sialyltransferase
1
(ST6GAL1).
By
evaluating
proteome,
N-glycome
extracted
using
different
methods,
UC
was
identified
as
optimal
approach
this
study,
it
offered
balance
between
operational
complexity,
cost-effectiveness,
preservation
activity.
In
total
1,928
high-confidence
over
84
were
quantified.
ST6GAL1
exhibited
consistent
upregulation
16
proteins,
downregulation
10
well
3
glycans.
Quantitative
analysis
revealed
that
overexpression
led
significant
cell
adhesion
glycosylation
pathways,
along
specific
changes
structures.
Notably,
these
modifications
extended
beyond
α2,6-sialylation,
suggesting
interactions
glycosyltransferases
may
drive
alterations.
Journal of Extracellular Vesicles,
Год журнала:
2024,
Номер
13(10)
Опубликована: Окт. 1, 2024
Abstract
The
morphogenesis
of
higher
plants
requires
communication
among
distant
organs
throughout
vascular
tissues
(xylem
and
phloem).
Numerous
investigations
have
demonstrated
that
phloem
also
act
as
a
distribution
route
for
signalling
molecules
being
observed
different
macromolecules
translocated
by
the
sap,
including
nucleic
acids
proteins,
change
under
stress
situations.
participation
extracellular
vesicles
(EVs)
in
this
has
been
suggested,
although
little
is
known
about
their
role.
In
fact,
last
decade,
presence
EVs
originated
great
controversy,
where
major
concerns
arose
from
origin,
isolation
methods,
even
appropriate
nomenclature
plant
nanovesicles.
Phloem
sap
exudates
melon
plants,
either
aphid‐free
or
infested
with
Aphis
gossypii
,
were
collected
stem
incision.
After
concentration
(Amicon),
(PhlEVs)
isolated
size
exclusion
chromatography.
PhlEVs
characterised
using
Nanoparticle
Tracking
Analysis,
Transmission
electron
microscopy
proteomic
analysis.
Here
we
confirm
vivo
detection
changes
particles/protein
ratio
composition
response
to
insect
feeding,
revealing
typical
defence
proteins
cargo
well
components
proteasome
complex.
showed
lower
almost
two
times
more
proteolytic
activity
than
plants.
both
cases,
such
was
inhibited
dose‐dependent
manner
inhibitor
MG132.
Our
results
suggest
may
use
mechanism
prepare
themselves
receive
infectious
agents
open
up
possibility
an
evolutionary
conserved
against
pathogens/stresses
eukaryotic
organisms.
Life Sciences,
Год журнала:
2024,
Номер
351, С. 122810 - 122810
Опубликована: Июнь 11, 2024
Cardiovascular
pathology
is
the
main
cause
of
death
in
chronic
kidney
disease
(CKD)
patients.
CKD
associated
with
accumulation
uremic
toxins
bloodstream,
and
indoxyl
sulfate
(IS)
one
most
abundant
found
blood
We
conducted
an
vitro
study
to
assess
mechanisms
underlying
IS-induced
endothelial
dysfunction
that
could
lead
cardiovascular
diseases.
also
studied
their
extracellular
vesicles
(EVs)
owing
capacity
act
as
messengers
transmit
signals
through
cargo.
EVs
were
characterized
by
nanoparticle
tracking
analysis,
transmission
electron
microscopy,
flow
cytometry,
tetraspanin
expression.
Cell
lysates
isolated
analyzed
using
liquid
chromatography
coupled
mass
spectrometry,
followed
Gene
Set
Enrichment
Analysis
identify
altered
pathways.
Proteomic
analysis
cells
revealed
IS
causes
increase
proteins
related
adipogenesis,
inflammation,
xenobiotic
metabolism
a
decrease
proliferation.
Extracellular
matrix
elements,
well
myogenesis,
response
UV
irradiation,
be
downregulated
IS-treated
EVs.
Fatty
acid
was
increased
along
adipogenesis
inflammation
observed
cells.
The
treatment
expression
less
Furthermore,
from
treated
may
mediate
dysfunction,
since
they
present
fewer
inflammatory
factors,
radiation.
Therapeutic Advances in Medical Oncology,
Год журнала:
2024,
Номер
16
Опубликована: Янв. 1, 2024
Circulating
tumor
cells
(CTCs)
are
that
slough
off
the
primary
lesions
and
extravasate
into
bloodstream.
By
forming
CTC
clusters
interacting
with
other
circulating
(platelets,
NK
cells,
macrophage,
etc.),
CTCs
able
to
survive
in
circulatory
system
of
patients
colonize
metastatic
organs.
In
recent
years,
potential
diagnosis,
prognostic
assessment,
individualized
therapy
various
types
tumors
has
been
gradually
explored,
while
advances
biotechnology
have
made
it
possible
extract
from
patient
blood
samples.
These
biological
features
provide
us
new
insights
cancer
vulnerabilities.
With
advent
immunotherapies
personalized
medicines,
disrupting
heterotypical
interaction
between
as
well
direct
targeting
hold
great
promise.
Pancreatic
(PC)
is
one
most
malignant
cancers,
part
because
early
metastasis,
difficult
limited
treatment
options.
Although
there
significant
for
a
biomarker
impact
PC
diagnosis
therapy,
still
remain
number
challenges
routine
implementation
clinical
management
PC.
this
review,
we
summed
up
progress
understanding
characteristics
exceptional
technological
provided
insight
exploiting
these
developments
design
future
tools
improving
Abstract
Background
Male
breast
cancer
(MBC)
is
a
rare
malignancy,
but
its
global
incidence
has
shown
notable
increase
in
recent
decades.
Factors
such
as
limited
health
literacy,
inadequate
education,
and
reluctance
to
seek
medical
attention
contribute
the
late-stage
diagnosis
of
most
MBC
patients.
Consequently,
there
an
urgent
need
for
highly
specific
sensitive
diagnostic
approach
MBC.
Methods
This
retrospective
study
enrolled
20
patients
with
30
surgical
or
biopsy
specimens
from
August
2020
2023.
The
90-gene
expression
assay
was
performed
determine
tissue
origin.
Predicted
tumor
types
were
then
compared
reference
accuracy
calculation.
differentially
expressed
genes
identified
between
male
female
cancer.
Result
demonstrated
overall
96.7%
(29/30)
when
pathological
diagnosis.
For
primary,
lymph
node
metastatic,
distant
metastatic
tumors,
accuracies
100%
(15/15),
90.9%
(10/11),
(4/4),
respectively.
Five
(
RPS4Y1
,
PI15
AZGP1
PRRX1
AGR2
)
up-regulated,
six
XIST
PIGR
SFRP1
PLA2G2A
S100A2
CHI3L1
down-regulated
Conclusion
Our
findings
highlight
promising
performance
accurately
identifying
origin
Incorporating
this
into
diagnoses
potential
empower
oncologists
precision
treatment
options,
ultimately
enhancing
care
outcomes
Filopodia
are
dynamic
adhesive
cytoskeletal
structures
that
critical
for
directional
sensing,
polarization,
cell-cell
adhesion,
and
migration
of
diverse
cell
types.
also
neuronal
synapse
formation.
While
rearrangement
the
actin
cytoskeleton
is
known
to
be
filopodia
biogenesis,
little
about
upstream
extracellular
signals.
Here,
we
identify
secreted
exosomes
as
potent
regulators
Inhibition
exosome
secretion
inhibited
formation
stabilization
in
both
cancer
cells
neurons
subsequent
by
neurons.
Rescue
experiments
with
purified
small
large
vesicles
(EVs)
identified
exosome-enriched
EVs
(SEVs)
having
filopodia-inducing
activity.
Proteomic
analyses
cell-derived
SEVs
TGF-β
family
coreceptor
endoglin
a
key
SEV-enriched
cargo
regulates
filopodia.
Cancer
levels
affected
filopodia-dependent
behaviors,
including
metastasis
chick
embryos
3D
collagen
gels.
As
do
not
express
endoglin,
performed
second
proteomics
experiment
SEV
cargoes
regulated
might
promote
We
discovered
single
was
altered
endoglin-KD
SEVs,
transmembrane
protein
Thrombospondin
Type
1
Domain
Containing
7A
(THSD7A).
further
found
carry
THSD7A
add-back
sufficient
rescue
defects
exosome-inhibited
find
induces
through
activation
Rho
GTPase,
Cdc42.
These
findings
suggest
new
model
formation,
triggered
carrying
THSD7A.
Filopodia
are
dynamic
adhesive
cytoskeletal
structures
that
critical
for
directional
sensing,
polarization,
cell-cell
adhesion,
and
migration
of
diverse
cell
types.
also
neuronal
synapse
formation.
While
rearrangement
the
actin
cytoskeleton
is
known
to
be
filopodia
biogenesis,
little
about
upstream
extracellular
signals.
Here,
we
identify
secreted
exosomes
as
potent
regulators
Inhibition
exosome
secretion
inhibited
formation
stabilization
in
both
cancer
cells
neurons
subsequent
by
neurons.
Rescue
experiments
with
purified
small
large
vesicles
(EVs)
identified
exosome-enriched
EVs
(SEVs)
having
filopodia-inducing
activity.
Proteomic
analyses
cell-derived
SEVs
TGF-β
family
coreceptor
endoglin
a
key
SEV-enriched
cargo
regulates
filopodia.
Cancer
levels
affected
filopodia-dependent
behaviors,
including
metastasis
chick
embryos
3D
collagen
gels.
As
do
not
express
endoglin,
performed
second
proteomics
experiment
SEV
cargoes
regulated
might
promote
We
discovered
single
was
altered
endoglin-KD
SEVs,
transmembrane
protein
Thrombospondin
Type
1
Domain
Containing
7A
(THSD7A).
further
found
carry
THSD7A
add-back
sufficient
rescue
defects
exosome-inhibited
find
induces
through
activation
Rho
GTPase,
Cdc42.
These
findings
suggest
new
model
formation,
triggered
carrying
THSD7A.