SDCBP Orchestrated Gastric Cancer Aggression Through Epithelial‐ Mesenchymal Transition and Macrophages M2 Polarization
Molecular Carcinogenesis,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 21, 2025
ABSTRACT
Gastric
cancer
remains
a
significant
global
health
burden
with
limited
treatment
options
and
high
mortality.
Syndecan‐binding
protein
(SDCBP),
scaffolding
involved
in
tumor
differentiation,
has
attracted
attention
as
potential
therapeutic
target
cancers.
However,
its
precise
role
gastric
progression
is
not
fully
understood.
In
this
study,
through
bioinformatics
analysis
samples
detection,
we
discovered
that
SDCBP
was
highly
expressed
tissues,
which
correlated
clinicopathological
features
such
invasion
depth
distant
metastasis,
exhibited
heterogeneity
across
histological
or
molecular
subtypes.
Elevated
expression
promoted
the
proliferation,
migration
of
cells,
modulated
epithelial‐mesenchymal
transition
(EMT)
via
ERK
signaling
pathway.
Xenograft
experiments
mice
confirmed
inhibiting
could
delay
progression.
We
also
found
cells
knockdown
were
able
to
inhibit
M2
polarization
cocultured
macrophages,
reduce
chemotaxis
enhance
phagocytosis
macrophages.
Therefore,
plays
crucial
driving
Targeting
can
partially
reverse
malignant
phenotype,
expected
be
promising
for
cancer.
Language: Английский
Comprehensive analysis of stearoyl-coenzyme A desaturase in prostate adenocarcinoma: insights into gene expression, immune microenvironment and tumor progression
Jie Wang,
No information about this author
Ying Liang,
No information about this author
He Xiong
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Sept. 16, 2024
Prostate
adenocarcinoma
(PRAD)
is
a
prevalent
global
malignancy
which
depends
more
on
lipid
metabolism
for
tumor
progression
compared
to
other
cancer
types.
Although
Stearoyl-coenzyme
A
desaturase
(SCD)
documented
regulate
in
multiple
cancers,
landscape
analysis
of
its
implications
PRAD
are
still
missing
at
present.
Here,
we
conducted
an
diverse
datasets
revealing
elevated
SCD
expression
the
cohort
both
mRNA
and
protein
levels.
Interestingly,
was
associated
with
promoter
hypermethylation
genetic
alterations,
notably
L134V
mutation.
Integration
comprehensive
immunological
genomic
data
revealed
robust
positive
correlation
between
levels
abundance
CD8
+
T
cells
macrophages.
Further
analyses
identified
significant
associations
various
immune
markers
microenvironment.
Single-cell
transcriptomic
profiling
unveiled
differential
patterns
across
distinct
cell
types
within
prostate
The
Gene
Ontology
Kyoto
Encyclopedia
Genes
Genome
showed
that
enriched
pathways
were
primarily
related
biosynthesis,
cholesterol
endoplasmic
reticulum
membrane
functions,
metabolic
pathways.
Set
Enrichment
Analysis
highlighted
involvement
crucial
cellular
processes,
including
cycle
biosynthesis
cofactors
In
functional
studies,
overexpression
promoted
proliferation,
metastasis
invasion
cells,
whereas
downregulation
inhibits
these
processes.
This
study
provides
insights
into
multifaceted
roles
pathogenesis,
underscoring
potential
as
therapeutic
target
prognostic
biomarker.
Language: Английский
Tumor-associated macrophages and CD8+ T cells: dual players in the pathogenesis of HBV-related HCC
Muhammad Naveed Khan,
No information about this author
Binli Mao,
No information about this author
Juan Hu
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Oct. 10, 2024
HBV
infection
is
a
key
risk
factor
for
the
development
and
progression
of
hepatocellular
carcinoma
(HCC),
highly
invasive
tumor,
characterized
by
its
persistent
immunosuppressive
microenvironment.
This
review
provides
an
in-depth
analysis
HBV-related
HCC
explores
interactions
between
neutrophils,
natural
killer
cells,
dendritic
examining
their
roles
in
regulating
tumor-associated
macrophages
CD8+
T
cells
shaping
tumor
Two
critical
players
milieu
are
(TAMs).
The
study
how
TAMs,
initially
recruited
to
combat
infection,
transform,
adopting
tumor-promoting
phenotype,
turning
against
body,
promoting
cell
proliferation,
suppressing
anti-tumor
immunity,
assisting
spread
cancer.
Meanwhile,
crucial
controlling
become
dysfunctional
exhausted
response
chronic
viral
inflammation.
then
dissects
TAMs
manipulate
this
immune
response,
further
depleting
functions
through
mechanisms
like
arginine
deprivation
creating
hypoxic
environments
that
lead
exhaustion.
Finally,
it
challenges
promising
therapeutic
avenues
target
either
separately
or
combination
with
antiviral
therapy
personalized
medicine
approaches,
offering
hope
improved
outcomes
HCC.
Language: Английский
Construction of a prognostic model for ovarian cancer based on a comprehensive bioinformatics analysis of cuproptosis-associated long non-coding RNA signatures
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(15), P. e35004 - e35004
Published: July 23, 2024
Ovarian
cancer
(OCa)
is
a
common
malignancy
in
women,
and
the
role
of
cuproptosis
its
related
genes
OCa
unclear.
Using
GSE14407
dataset,
we
analyzed
expression
correlation
cuproptosis-related
(CRGs)
between
tumor
normal
groups.
From
TCGA-OV
identified
20
long
non-coding
RNAs
(CuLncs)
associated
with
patient
survival
through
univariate
Cox
analysis.
patients
were
divided
into
early-stage
late-stage
groups
to
analyze
CuLncs
expression.
Cluster
analysis
classified
two
clusters,
Cluster1
having
poorer
prognosis.
Significant
differences
"Lymphatic
Invasion"
"Cancer
status"
observed
clusters.
Seven
CRGs
showed
significant
differences,
validated
using
human
protein
atlas
(HPA)
databases.
Immune
revealed
higher
ImmuneScore
Cluster1.
GSEA
signaling
pathways.
LASSO
regression
included
11
construct
validate
prediction
model,
classifying
high-risk
low-risk
Correlations
riskScore,
phenotype,
ImmuneScore,
immune
cell
infiltration
explored.
Cell
experiments
that
knocking
down
AC023644.1
decreases
viability.
In
conclusion,
constructed
an
accurate
prognostic
model
for
based
on
CuLncs,
providing
basis
prognosis
assessment
potential
immunotherapy
targets.
Language: Английский
Exploring SSR1 as a novel diagnostic and prognostic biomarker in hepatocellular carcinoma, and its relationship with immune infiltration
Qingyu Xiao,
No information about this author
Wen Qü,
No information about this author
Wen-Ying Shen
No information about this author
et al.
Translational Cancer Research,
Journal Year:
2024,
Volume and Issue:
13(10), P. 5278 - 5299
Published: Oct. 1, 2024
Although
signal
sequence
receptor
subunit
1
(SSR1)
has
undergone
thorough
examination
in
different
cancer
types,
its
importance
hepatocellular
carcinoma
(HCC)
remains
largely
uncharted
and
warrants
further
investigation.
The
aim
of
this
study
is
to
explore
the
role
SSR1
HCC
progression
decipher
underlying
molecular
mechanisms.
Language: Английский