A novel high‐risk model identified by epithelial–mesenchymal transition predicts prognosis and radioresistance in rectal cancer
Feiyu Qin,
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Zehua Bian,
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Lingzhen Jiang
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et al.
Molecular Carcinogenesis,
Journal Year:
2024,
Volume and Issue:
63(11), P. 2119 - 2132
Published: July 26, 2024
Many
studies
have
shown
that
tumor
cells
survive
radiotherapy
are
more
likely
to
metastasize,
but
the
underlying
mechanism
remains
unclear.
Here
we
aimed
identify
epithelial-mesenchymal
transition
(EMT)-related
key
genes,
which
associated
with
prognosis
and
radiosensitivity
in
rectal
cancer.
First,
obtained
differentially
expressed
genes
by
analyzing
RNA
expression
profiles
of
cancer
retrieved
from
The
Cancer
Genome
Atlas
database,
EMT-related
radiotherapy-related
databases,
respectively.
Then,
Lasso
Cox
regression
analyses
were
used
establish
an
model
(EMTPM)
based
on
identified
independent
protective
factor
Fibulin5
(FBLN5)
risk
gene
EHMT2.
high-EMTPM
group
exhibited
significantly
poorer
prognosis.
evaluated
signature
external
clinical
validation
cohort.
Through
vivo
experiments,
further
demonstrated
EMTPM
effectively
distinguishes
radioresistant
radiosensitive
patients
Moreover,
individuals
showed
increased
immune
checkpoints
compared
their
counterparts.
Finally,
pan-cancer
analysis
also
indicated
its
potential
for
predicting
lung
squamous
cell
carcinoma
breast
undergoing
radiotherapy.
In
summary,
established
a
novel
predictive
radioresistance
FBLN5
EHMT2
expressions,
suggested
microenvironment
may
be
involved
process
radioresistance.
This
could
select
management
strategies
Language: Английский
Blood TCTP as a potential biomarker associated with immunosuppressive features and poor clinical outcomes in metastatic gastric cancer
Journal for ImmunoTherapy of Cancer,
Journal Year:
2025,
Volume and Issue:
13(3), P. e010455 - e010455
Published: March 1, 2025
Background
No
established
biomarker
exists
for
specific
myeloid
cell
populations
or
in
gastric
cancer.
This
study
aimed
to
explore
the
prognostic
and
immunological
relevance
of
plasma
translationally
controlled
tumor
protein
(TCTP)
patients
with
advanced
cancer
treated
an
immune
checkpoint
inhibitor
and/or
cytotoxic
chemotherapy.
Methods
Plasma
samples
were
prospectively
collected
from
cohorts
first-line
fluoropyrimidine
plus
platinum
chemotherapy
(n=143,
cohort
1)
third-line
nivolumab
(n=165,
2).
TCTP
levels
quantified
using
ELISA,
multiplex
proteomic
analysis
(Olink)
was
conducted
assess
expression
immune-related
proteins.
External
single-cell
RNA
sequencing
(scRNA-seq)
spatial
transcriptomics
datasets
employed
validate
findings.
Results
Patients
high
(TCTP-high
group)
exhibited
poor
progression-free
survival
(PFS)
overall
(OS)
compared
those
low
(TCTP-low
1
(HR:
1.73
PFS;
1.77
OS).
In
TCTP-high
group,
proteins
associated
immunosuppressive
cells,
angiogenesis,
exclusion
T/natural
killer
(NK)
function
upregulated,
whereas
involved
T-cell
activation/exhaustion
significantly
upregulated
TCTP-low
group.
scRNA-seq
analyses
identified
a
subset
TPT1
(encoding
TCTP)
TCTP-related
molecules,
enriched
inhibitory
inflammation
gene
signatures
providing
signals
T/NK
cells
(Macrophage-chemokine).
Spatial
revealed
tumor-cell-enriched
cluster
co-localized
Macrophage-chemokine
subset,
which
highest
positive
correlation
between
its
abundance
average
levels.
nivolumab-treated
(cohort
2),
group
outcomes
1.39
1.47
Conclusions
is
biomarker,
reflecting
clinically
relevant
Language: Английский
Identification and validation of matrix metalloproteinase hub genes as potential biomarkers for Skin Cutaneous Melanoma
Frontiers in Oncology,
Journal Year:
2024,
Volume and Issue:
14
Published: Oct. 18, 2024
Objectives
The
role
of
matrix
metalloproteinases
(MMPs)
in
Skin
Cutaneous
Melanoma
(SKCM)
development
and
progression
is
unclear
so
far.
This
comprehensive
study
delved
into
the
intricate
MMPs
SKCM
progression.
Methods
RT-qPCR,
bisulfite
sequencing,
WES
analyzed
MMP
gene
expression,
promoter
methylation,
mutations
cell
lines.
TCGA
datasets
validated
findings.
DrugBank
molecular
docking
identified
potential
regulatory
drugs,
line
experiments
confirmed
key
genes
tumorigenesis.
Results
Our
findings
unveiled
significant
up-regulation
MMP9,
MMP12,
MMP14,
MMP16,
coupled
with
hypomethylation
their
promoters
lines,
implicating
involvement
disease
Mutational
analysis
highlighted
a
low
frequency
these
genes,
indicating
less
expression
mechanisms.
Prognostic
assessments
showcased
correlation
between
elevated
poor
overall
survival
(OS)
patients.
Additionally,
functional
involving
silencing
revealed
impact
on
cellular
proliferation,
further
emphasizing
significance
MMP16
pathobiology.
Conclusion
identifies
Estradiol
Calcitriol
as
drugs
for
modulating
SKCM,
highlighting
diagnostic
prognostic
biomarkers.
Language: Английский
PPIC-labeled CAFs: Key players in neoadjuvant chemotherapy resistance for gastric cancer
Honghao Yin,
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Lili Sun,
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Yuan Yuan
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et al.
Translational Oncology,
Journal Year:
2024,
Volume and Issue:
48, P. 102080 - 102080
Published: Aug. 7, 2024
Gastric
cancer
(GC)
is
the
fourth
leading
cause
of
deaths,
with
advanced
cases
having
a
median
survival
less
than
one
year.
Neoadjuvant
chemotherapy
(NCT)
vital
but
faces
drug
resistance
issues,
partly
due
to
cancer-associated
fibroblasts
(CAFs).
Yet,
specific
CAF
subpopulations
contributing
are
poorly
understood.
Language: Английский
Advances in the diagnosis and treatment of MET-variant digestive tract tumors
World Journal of Gastrointestinal Oncology,
Journal Year:
2024,
Volume and Issue:
16(11), P. 4338 - 4353
Published: Oct. 25, 2024
The
receptor
tyrosine
kinase
encoded
by
the
MET
gene
plays
an
important
role
in
various
cellular
processes
such
as
growth,
survival,
migration
and
angiogenesis,
its
abnormal
activation
is
closely
related
to
occurrence
development
of
tumors.
This
article
reviews
recent
advances
diagnosis
treatment
MET-variant
digestive
tract
In
terms
diagnosis,
application
next-generation
sequencing
technology
liquid
biopsy
makes
detection
variants
more
accurate
efficient,
providing
a
reliable
basis
for
individualized
treatment.
treatment,
inhibitors
crizotinib
cabotinib
have
shown
good
efficacy
clinical
trials.
addition,
combination
immunotherapy
also
demonstrated
potential
synergies,
further
improving
therapeutic
effect.
However,
complexity
heterogeneity
drug
resistance
mechanisms
are
still
one
difficulties
current
research.
future,
it
necessary
deepen
understanding
mechanism
variation
explore
new
strategies
improve
overall
survival
rate
quality
life
patients.
tumors
moving
towards
precision
individualization,
broad
prospects.
Language: Английский