Aging,
Journal Year:
2022,
Volume and Issue:
14(24), P. 10067 - 10080
Published: Dec. 20, 2022
Starving
intratumoral
microenvironment
prominently
alters
genic
profiles
including
long
non-coding
RNAs
(lncRNAs),
which
further
regulate
bladder
cancer
(BCa)
malignant
biological
properties,
such
as
invasion
and
migration.Transcriptome
RNA-sequencing
data
of
414
BCa
tumor
tissues
19
normal
were
obtained
from
TCGA
database
paired
samples
132
patients.
A
chain
in
vitro
validations
qPCR,
migration
assays
performed
to
reveal
the
clinical
relevance
AC011472.4
AL157895.1.A
total
11
lncRNAs
identified
starvation-related
lncRNAs,
AL157895.1
relevant
overall
survival
Besides,
a
risk
score
model
was
established
based
on
levels
AL157895.1.
patients
with
higher
divided
into
high-risk
group
usually
mortality
rate,
but
contrary.
expressed
highly
cell
lines
tumour
tissues,
especially
advanced
grade,
stage
T-stage,
while
showed
reversed
result.
Moreover,
increased
level
remarkably
correlated
muscle
status
distant
metastasis.
SiRNAs-mediated
silence
respectively
diminished
properties
cells.In
this
study,
we
highlight
significant
roles
evaluating
prognoses
validate
their
correlation
various
parameters.
These
findings
provide
an
appropriate
for
decision
making.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: Nov. 6, 2023
Background
Pre-mRNA
processing
factor
19
(PRPF19)
is
an
E3
ligase
that
plays
a
crucial
role
in
repairing
tumor-damaged
cells
and
promoting
cell
survival.
However,
the
predictive
value
biological
function
of
PRPF19
bladder
urothelial
carcinoma
(BLCA)
require
further
investigation.
Methods
In
this
study,
we
utilized
transcriptomic
data
cancer
tissue
microarrays
to
identify
high
expression
BLCA,
suggesting
its
potential
as
prognostic
biomarker.
To
gain
better
understanding
immune
microenvironment
performed
single
analysis
employed
LASSO
method.
Additionally,
examined
methylation
profiles
using
SMART
website.
Our
investigation
confirmed
correlation
between
BLCA
senescence
stemness.
Furthermore,
constructed
PRPF19-miR-125a-5p-LINC02693-MIR4435-2HG
ceRNA
network
ENCORI
miRWALK
databases.
Results
comprehensive
reveals
can
serve
marker
for
significantly
associated
with
various
immune-infiltrating
BLCA.
Moreover,
our
findings
suggest
influences
cellular
through
regulation
Finally,
developed
has
predict
prognosis
patients.
Conclusion
We
multiple
functions
specific
be
used
therapeutic
target
Cell Metabolism,
Journal Year:
2024,
Volume and Issue:
36(7), P. 1619 - 1633.e5
Published: July 1, 2024
Population-level
variation
and
mechanisms
behind
insulin
secretion
in
response
to
carbohydrate,
protein,
fat
remain
uncharacterized.
We
defined
prototypical
responses
three
macronutrients
islets
from
140
cadaveric
donors,
including
those
with
type
2
diabetes.
The
majority
of
donors'
exhibited
the
highest
glucose,
moderate
amino
acid,
minimal
fatty
acid.
However,
9%
had
acid
responses,
8%
that
were
larger
than
their
glucose-stimulated
responses.
leveraged
this
heterogeneity
used
multi-omics
identify
molecular
correlates
nutrient
responsiveness,
as
well
proteins
mRNAs
altered
also
examined
nutrient-stimulated
release
stem
cell-derived
observed
responsiveness
but
not
carbohydrate
or
protein-potentially
a
hallmark
immaturity.
Understanding
diversity
lays
groundwork
for
personalized
nutrition.
Journal of Cellular and Molecular Medicine,
Journal Year:
2024,
Volume and Issue:
28(10)
Published: May 1, 2024
Abstract
Smoking
is
a
well‐known
risk
factor
for
non‐small‐cell
lung
cancer
(NSCLC)
and
bladder
urothelial
carcinoma
(BLCA).
Despite
this,
there
has
been
no
investigation
into
prognostic
marker
based
on
smoking‐related
genes
that
could
universally
predict
prognosis
in
these
cancers
correlate
with
immune
checkpoint
therapy.
This
study
aimed
to
identify
differential
NSCLC
BLCA,
analyse
their
roles
patient
therapy
through
subgroup
analyses,
shed
light
PRR11
as
crucial
gene
both
cancers.
By
examining
co‐expressed
genes,
model
was
constructed
its
impact
immunotherapy
BLCA
evaluated.
Molecular
docking
tissue
microarray
analyses
were
conducted
explore
the
correlation
between
reciprocal
SPDL1.
Additionally,
miRNAs
associated
analysed.
The
confirmed
strong
link
prognosis,
BLCA.
identified
key
smoking‐associated
influences
efficacy
of
by
modulating
stemness
A
established
value
validated
NSCLC.
Furthermore,
it
found
regulates
PDL1
via
SPDL1,
impacting
immunotherapeutic
involvement
hsa‐miR‐200b‐3p
regulation
SPDL1
expression
also
highlighted.
Overall,
elucidates
modulates
influencing
interaction
potential
upstream
hsa‐miR‐200b‐3p.
Aging,
Journal Year:
2023,
Volume and Issue:
unknown
Published: July 10, 2023
Patients
with
advanced
bladder
cancer
gradually
become
less
sensitive
to
chemotherapeutic
agents,
leading
tumor
recurrence.
Initiating
the
senescence
program
in
solid
tumors
may
be
an
important
means
of
improving
short-term
drug
sensitivity.
The
role
c-Myc
cell
was
determined
using
bioinformatics
methods.
response
cisplatin
chemotherapy
sample
analyzed
according
Genomics
Drug
Sensitivity
Cancer
database.
Cell
Counting
Kit-8
assay,
clone
formation
and
senescence-associated
β-galactosidase
staining
were
used
assess
growth,
senescence,
sensitivity
cisplatin,
respectively.
Western
blot
immunoprecipitation
performed
understand
regulation
p21
by
c-Myc/HSP90B1.
Bioinformatic
analysis
showed
that
c-Myc,
a
cellular
gene,
significantly
associated
prognosis
chemotherapy.
HSP90B1
expression
highly
correlated
cancer.
Reducing
level
inhibited
proliferation,
promoted
enhanced
chemosensitivity.
Immunoprecipitation
assays
confirmed
interacted
c-Myc.
reducing
could
redeem
overexpression
caused
overexpression.
Further
studies
alleviate
rapid
growth
accelerate
cells
overexpression,
levels
also
improve
cells.
HSP90B1/c-Myc
interaction
regulates
signaling
pathway,
which
affects
chemosensitivity
modulating
senescence.
Frontiers in Oncology,
Journal Year:
2025,
Volume and Issue:
14
Published: Jan. 9, 2025
Gliomas,
particularly
glioblastomas
(GBM),
are
highly
aggressive
with
a
poor
prognosis
and
low
survival
rate.
Currently,
deoxyelephantopin
(DET)
has
shown
promising
anti-inflammatory
anti-tumor
effects.
Using
clinical
prognostic
analysis,
molecular
docking,
network
pharmacology,
this
study
aims
to
explore
the
primary
targets
signaling
pathways
identify
novel
GBM
treatment
approaches.
PharmMapper,
chemical
structure
of
DET
was
examined
for
possible
after
being
acquired
from
PubChem.
GBM-related
were
obtained
through
multi-omics
A
protein-protein
interaction
(PPI)
constructed
using
Cytoscape
STRING,
target
binding
evaluated
docking.
Enrichment
analysis
conducted
Metascape.
The
effects
on
cell
invasion,
apoptosis,
proliferation
assessed
in
vitro
assays,
including
Transwell,
EDU,
CCK8,
flow
cytometry.
Western
blot
performed
examine
components
PI3K/AKT
pathway.
Among
sixty-four
shared
identified,
JUN
CCND1
most
frequently
observed.
demonstrated
that
influenced
MAPK
pathways.
In
Transwell
significantly
inhibited
invasive
behavior
glioma
cells.
further
confirmed
downregulation
EGFR,
JUN,
PI3K/AKT.
inhibits
proliferation,
apoptosis
via
modulating
pathway,
highlighting
its
potential
as
therapeutic
strategy
treatment.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 28, 2025
Breast
cancer
(BC)
is
the
most
common
in
women
and
a
leading
cause
of
cancer-related
mortality.
Despite
advances
screening
treatment,
outcomes
for
advanced
or
recurrent
BC
remain
poor,
highlighting
need
new
strategies.
Recent
research
emphasizes
tumor
microenvironment
(TME),
particularly
tumor-associated
macrophages
(TAMs),
as
key
drivers
growth,
metastasis,
resistance
to
therapy.
The
presence
M2-like
TAMs
TME
promotes
immune
evasion
progression
across
subtypes.
This
review
summarizes
classification,
their
role
BC,
emerging
therapies
targeting
TAMs,
including
depletion,
inhibition
recruitment,
reprogramming
from
pro-tumoral
M2
anti-tumoral
M1
phenotypes.
Targeting
offers
promising
strategy
improve
treatment
outcomes.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 17, 2025
Breast
cancer
(BC)
is
a
predominant
malignancy
among
women
globally,
with
its
etiology
remaining
largely
elusive.
Diagnosis
primarily
relies
on
invasive
histopathological
methods,
which
are
often
limited
by
sample
representation
and
processing
time.
Consequently,
non-invasive
imaging
techniques
such
as
mammography,
ultrasound,
Magnetic
Resonance
Imaging
(MRI)
indispensable
for
BC
screening,
diagnosis,
staging,
treatment
monitoring.
Recent
advancements
in
technologies
artificial
intelligence-driven
radiomics
have
enhanced
precision
medicine
enabling
early
detection,
accurate
molecular
subtyping,
personalized
therapeutic
strategies.
Despite
reductions
mortality
through
traditional
treatments,
challenges
like
tumor
heterogeneity
resistance
persist.
Immunotherapies,
particularly
PD-1/PD-L1
inhibitors,
emerged
promising
alternatives.
This
review
explores
recent
developments
diagnostics
immunotherapeutic
approaches,
aiming
to
inform
clinical
practices
optimize
outcomes.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 21, 2025
Colon
cancer
(CC)
remains
a
primary
contributor
to
cancer-related
fatalities
worldwide,
driven
by
difficulties
in
early
diagnosis
and
constrained
therapeutic
options.
Recent
studies
underscore
the
importance
of
tumor
microenvironment
(TME),
notably
tumor-associated
macrophages
(TAMs),
fostering
malignancy
progression
therapy
resistance.
Through
their
inherent
plasticity,
TAMs
facilitate
immunosuppression,
angiogenic
processes,
metastatic
spread,
drug
tolerance.
In
contrast
M1
macrophages,
which
promote
inflammatory
tumoricidal
responses,
M2
support
expansion
dissemination
exerting
immunosuppressive
pro-angiogenic
influences.
Consequently,
manipulating
has
emerged
as
potential
avenue
enhance
treatment
effectiveness.
This
review
outlines
origins,
polarization
states,
functions
CC,
highlights
role
driving
advancement,
surveys
ongoing
efforts
target
these
cells
for
better
patient
outcomes.
Emerging
strategies
aimed
at
modulating
TAM
-
including
depletion
strategies,
reprogramming
approaches
that
shift
M2-polarized
toward
an
phenotype,
inhibition
key
signaling
pathways
sustaining
TAM-mediated
immunosuppression-are
currently
under
active
investigation.
These
hold
promise
overcoming
induced
resistance
improving
immunotherapeutic
efficacy
CC.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 27, 2025
Brain
metastasis
in
breast
cancer
(BCBM)
significantly
threatens
the
survival
and
quality
of
life
patients,
particularly
those
with
triple-negative
(TNBC)
HER2-positive
subtypes.
It
involves
complex
molecular
mechanisms
diverse
signaling
pathways.
This
review
highlights
recent
research
on
pathways
BCBM.
The
process
BCBM
includes
several
key
steps:
local
infiltration
cells
into
bloodstream
subsequent
spread
to
brain.
They
must
then
overcome
blood-brain
barrier
(BBB)
establish
grow
Multiple
pathways,
including
PI3K/AKT,
STAT3,
NF-κB,
Notch,
Wnt
are
involved
this
process.
Overall,
is
a
disease
regulated
by
multiple
To
improve
patient
life,
it
crucial
deepen
explore
new
treatment
targets
strategies.
will
enhance
our
understanding
lead
more
effective
treatments.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 2, 2025
Hepatocellular
carcinoma
(HCC)
remains
a
leading
cause
of
cancer-related
mortality
globally.
The
tumor
microenvironment
(TME)
plays
pivotal
role
in
HCC
progression,
characterized
by
dynamic
interactions
between
stromal
components,
immune
cells,
and
cells.
Key
players,
including
tumor-associated
macrophages
(TAMs),
tumor-infiltrating
lymphocytes
(TILs),
cytotoxic
T
(CTLs),
regulatory
cells
(Tregs),
MDSCs,
dendritic
(DCs),
natural
killer
(NK)
contribute
to
evasion
progression.
Recent
advances
immunotherapy,
such
as
checkpoint
inhibitors
(ICIs),
cancer
vaccines,
adoptive
cell
therapy
(ACT),
combination
therapies,
have
shown
promise
enhancing
anti-tumor
responses.
Dual
ICI
combinations,
ICIs
with
molecular
targeted
drugs,
integration
local
treatments
or
radiotherapy
demonstrated
improved
outcomes
patients.
This
review
highlights
the
evolving
understanding
therapeutic
potential
immunotherapeutic
strategies
management.