EXO1 is a key gene for lung-resident memory T cells and has diagnostic and predictive values for lung adenocarcinoma
Zhuoqi Li,
No information about this author
Xiaoyan Lin,
No information about this author
Yang Yang
No information about this author
et al.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Feb. 1, 2025
Lung
adenocarcinoma
(LUAD)
is
a
very
common
and
lethal
kind
of
lung
malignancy.
An
increasing
number
studies
indicated
that
tissue-resident
memory
T
(TRM)
cells
played
significant
roles
in
anti-cancer
immunity.
In
our
previous
study,
EXO1
was
found
to
be
core
gene
for
TRM
the
prognosis
LUAD.
However,
tumor
microenvironment,
its
application
diagnosis
prediction
LUAD
are
still
inadequately
explored.
this
RNA
expression,
DNA
methylation,
CNV,
somatic
mutation
data
EXO1,
corresponding
patients'
clinical
information
from
publicly
available
databases
were
analyzed
using
bioinformatic
methods.
The
results
validated
through
immunohistochemical
staining
samples.
showed
aberrantly
highly
expressed
tissues.
High
expression
risky
factor
patients.
level
associated
with
many
features
such
as
TNM
stages.
It
can
also
distinguish
normal
tissues
accurately.
correlated
infiltration
immune
cells,
high
an
adverse
effect
on
patients
receiving
anti-PD-1/PD-L1
immunotherapy.
Moreover,
had
worse
DSS,
DFI
PFI.
Language: Английский
A novel classification method for LUAD that guides personalized immunotherapy on the basis of the cross-talk of coagulation- and macrophage-related genes
Zhuoqi Li,
No information about this author
Ling Chen,
No information about this author
Zhigang Wei
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 13, 2025
Purpose
The
coagulation
process
and
infiltration
of
macrophages
affect
the
progression
prognosis
lung
adenocarcinoma
(LUAD)
patients.
This
study
was
designed
to
explore
novel
classification
methods
that
better
guide
precise
treatment
LUAD
patients
on
basis
macrophages.
Methods
Weighted
gene
coexpression
network
analysis
(WGCNA)
applied
identify
M2
macrophage-related
genes,
TAM
marker
genes
were
acquired
through
scRNA-seq
data.
MSigDB
KEGG
databases
used
obtain
coagulation-associated
genes.
intersecting
defined
as
(COMAR)
Unsupervised
clustering
evaluate
distinct
COMAR
patterns
for
R
package
“limma”
differentially
expressed
(DEGs)
between
patterns.
A
prognostic
risk
score
model,
which
validated
external
data
cohorts
clinical
samples,
constructed
DEGs.
Results
In
total,
33
obtained,
three
subtypes
identified
There
341
DEGs
subtypes,
60
selected
constructing
model.
Finally,
15
prognosis-associated
(CORO1A,
EPHA4,
FOXM1,
HLF,
IFIH1,
KYNU,
LY6D,
MUC16,
PPARG,
S100A8,
SPINK1,
SPINK5,
SPP1,
VSIG4,
XIST)
included
in
efficient
robust
predicting
patient
outcomes
receiving
anti-PD-1/PD-L1
immunotherapy.
Conclusions
can
be
classified
into
according
may
provide
guidance
treatment.
Language: Английский
Discovering the Potential Role of the C2 DUSP2+ MCs Subgroup in Lung Adenocarcinoma
Shengyi Zhang,
No information about this author
Xinhan Li,
No information about this author
Zhikai Xiahou
No information about this author
et al.
Translational Oncology,
Journal Year:
2025,
Volume and Issue:
54, P. 102295 - 102295
Published: Feb. 26, 2025
Language: Английский
Clinical significance and immune landscape analyses of the coagulation-related gene signatures in gastric cancer
Journal of Cancer,
Journal Year:
2025,
Volume and Issue:
16(6), P. 1971 - 1986
Published: March 3, 2025
Gastric
cancer
(GC)
is
one
of
the
most
common
types
clinically
malignant
tumors
and
a
global
health
challenge
due
to
its
high
mortality
poor
prognosis.
The
coagulation
cascade
closely
related
GC
plays
key
role
in
tumor
immune
microenvironment.
However,
specific
mechanisms
by
which
coagulation-related
genes
involved
occurrence
development
remains
unclear.
data
patients
were
obtained
from
TCGA
GSEA
databases,
respectively.
After
univariate
Cox
regression
analysis,
non-negative
matrix
factorization
method
was
used
identify
molecular
subtypes.
categorized
into
high-risk
low-risk
score
groups
based
on
median
risk
scores,
included
six
(PCDHAC1,
HABP2,
GPC3,
GFRA1,
F5,
DKK1).
There
significant
difference
survival
between
two
groups,
predictive
abilities
for
1-,
3-,
5-year
valid.
Here,
we
demonstrated
that
gene
signatures
are
valuable
predicting
patients.
Besides,
high-
grouping
also
better
reflects
status
mutation
burden
characteristics
infiltration
GC,
provides
theoretical
basis
individualized
chemotherapy
immunotherapy
Language: Английский