medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Oct. 5, 2023
Abstract
Background
Diffuse
large
B-cell
lymphoma
(DLBCL)
is
the
predominant
type
of
malignant
lymphoma.
Although
various
treatments
have
been
developed,
limited
efficacy
calls
for
more
and
further
exploration
its
characteristics.
Methods
Datasets
from
Gene
Expression
Omnibus
(GEO)
database
were
used
identifying
tumor
purity
DLBCL.
Survival
analysis
was
employed
analyzing
prognosis
DLBCL
patients.
Immunohistochemistry
conducted
to
detect
important
factor
that
influenced
prognosis.
Drug
sensitive
prediction
performed
evaluate
value
constructed
model.
Results
VCAN,
CD3G
C1QB
identified
as
three
key
genes
impacted
outcome
patients
both
in
GEO
datasets
samples
our
center.
Among
them,
VCAN
CD3G+
T
cells
correlated
with
favorable
prognosis,
worse
The
ratio
CD68+
macrophages
CD8+
associated
better
In
addition,
significantly
macrophages,
CD4+
ratio,
indicating
it
could
play
an
role
anti-tumor
immunity
riskScore
model
based
on
RNASeq
data
work
well
predicting
drug
sensitivity.
Conclusion
DLBCL,
also
exert
certain
impact
sensitivity
Aging,
Journal Year:
2023,
Volume and Issue:
15(21), P. 11831 - 11844
Published: Oct. 25, 2023
Metastasis
of
gastric
cancer
(GC)
is
one
the
major
causes
death
among
GC
patients.
metastasis
involves
numerous
biological
processes,
yet
specific
molecular
mechanisms
have
not
been
elucidated.
Here,
we
report
a
novel
tumor
suppressor,
retinoic
acid-induced
2
(RAI2),
which
located
in
Xp22
region
chromosome
and
plays
role
inhibiting
growth
invasion.
In
this
study,
integrated
analysis
The
Cancer
Genome
Atlas
(TCGA),
Gene
Expression
Omnibus
(GEO)
datasets
immunohistochemistry
staining
data
suggested
that
RAI2
expression
samples
was
low.
Moreover,
immune
infiltration
indicated
low
associated
with
higher
intensity
tumor-infiltrating
lymphocytes
(TILs)
an
abundance
Programmed
ligand
1
(PD-L1)
expression.
set
enrichment
(GSEA)
further
revealed
regulated
some
pathways
including
GAP
junction,
focal
adhesion
ECM
receptor
interaction
pathway,
regulation,
PI3K-Akt
signaling,
MAPK
cell
cycle,
DNA
replication.
Furthermore,
knockdown
promoted
proliferation,
migration,
invasion
vitro.
Taken
together,
these
results
suggest
suppressor
could
be
potential
target
for
development
anti-cancer
strategies
GC.
Background:
Diffuse
large
B-cell
lymphoma
(DLBCL)
is
the
predominant
type
of
malignant
lymphoma.
Although
various
treatments
have
been
developed,
limited
efficacy
calls
for
more
and
further
exploration
its
characteristics.
Methods:
Datasets
from
Gene
Expression
Omnibus
(GEO)
database
were
used
identifying
tumor
purity
DLBCL.
Survival
analysis
was
employed
analyzing
prognosis
DLBCL
patients.
Immunohistochemistry
conducted
to
detect
important
factors
that
influenced
prognosis.
Drug-sensitive
prediction
performed
evaluate
value
model.
Results:
VCAN,
CD3G,
C1QB
identified
as
three
key
genes
impacted
outcome
patients
both
in
GEO
datasets
samples
our
center.
Among
them,
VCAN
CD3G+
T
cells
correlated
with
favorable
prognosis,
worse
The
ratio
CD68
+
macrophages
CD8
associated
better
In
addition,
CD3G+T
significantly
macrophages,
CD4
cells,
+T
ratio,
indicating
it
could
play
an
role
anti-tumor
immunity
riskScore
model
constructed
based
on
RNASeq
data
C1QB,
CD3G
work
well
predicting
drug
sensitivity.
Conclusions:
DLBCL,
also
exert
certain
impact
sensitivity
Funding:
This
supported
by
Shenzhen
High-level
Hospital
Construction
Fund
CAMS
Innovation
Medical
Sciences
(CIFMS)
(2022-I2M-C&T-B-062).
Diffuse
large
B-cell
lymphoma
(DLBCL)
is
the
predominant
type
of
malignant
lymphoma.
Although
various
treatments
have
been
developed,
limited
efficacy
calls
for
more
and
further
exploration
its
characteristics.Datasets
from
Gene
Expression
Omnibus
(GEO)
database
were
used
identifying
tumor
purity
DLBCL.
Survival
analysis
was
employed
analyzing
prognosis
DLBCL
patients.
Immunohistochemistry
conducted
to
detect
important
factor
that
influenced
prognosis.
Drug
sensitive
prediction
performed
evaluate
value
constructed
model.VCAN,
CD3G
C1QB
identified
as
three
key
genes
impacted
outcome
patients
both
in
GEO
datasets
samples
our
center.
Among
them,
VCAN
CD3G+
T
cells
correlated
with
favorable
prognosis,
worse
The
ratio
CD68+
macrophages
CD8+
associated
better
In
addition,
significantly
macrophages,
CD4+
ratio,
indicating
it
could
play
an
role
anti-tumor
immunity
riskScore
model
based
on
RNASeq
data
VCAN,
work
well
predicting
drug
sensitivity.VCAN,
DLBCL,
also
exert
certain
impact
sensitivity
Diffuse
large
B-cell
lymphoma
(DLBCL)
is
the
predominant
type
of
malignant
lymphoma.
Although
various
treatments
have
been
developed,
limited
efficacy
calls
for
more
and
further
exploration
its
characteristics.Datasets
from
Gene
Expression
Omnibus
(GEO)
database
were
used
identifying
tumor
purity
DLBCL.
Survival
analysis
was
employed
analyzing
prognosis
DLBCL
patients.
Immunohistochemistry
conducted
to
detect
important
factor
that
influenced
prognosis.
Drug
sensitive
prediction
performed
evaluate
value
constructed
model.VCAN,
CD3G
C1QB
identified
as
three
key
genes
impacted
outcome
patients
both
in
GEO
datasets
samples
our
center.
Among
them,
VCAN
CD3G+
T
cells
correlated
with
favorable
prognosis,
worse
The
ratio
CD68+
macrophages
CD8+
associated
better
In
addition,
significantly
macrophages,
CD4+
ratio,
indicating
it
could
play
an
role
anti-tumor
immunity
riskScore
model
based
on
RNASeq
data
VCAN,
work
well
predicting
drug
sensitivity.VCAN,
DLBCL,
also
exert
certain
impact
sensitivity
Diffuse
large
B-cell
lymphoma
(DLBCL)
is
the
predominant
type
of
malignant
lymphoma.
Although
various
treatments
have
been
developed,
limited
efficacy
calls
for
more
and
further
exploration
its
characteristics.Datasets
from
Gene
Expression
Omnibus
(GEO)
database
were
used
identifying
tumor
purity
DLBCL.
Survival
analysis
was
employed
analyzing
prognosis
DLBCL
patients.
Immunohistochemistry
conducted
to
detect
important
factor
that
influenced
prognosis.
Drug
sensitive
prediction
performed
evaluate
value
constructed
model.VCAN,
CD3G
C1QB
identified
as
three
key
genes
impacted
outcome
patients
both
in
GEO
datasets
samples
our
center.
Among
them,
VCAN
CD3G+
T
cells
correlated
with
favorable
prognosis,
worse
The
ratio
CD68+
macrophages
CD8+
associated
better
In
addition,
significantly
macrophages,
CD4+
ratio,
indicating
it
could
play
an
role
anti-tumor
immunity
riskScore
model
based
on
RNASeq
data
VCAN,
work
well
predicting
drug
sensitivity.VCAN,
DLBCL,
also
exert
certain
impact
sensitivity
Background:
Diffuse
large
B-cell
lymphoma
(DLBCL)
is
the
predominant
type
of
malignant
lymphoma.
Although
various
treatments
have
been
developed,
limited
efficacy
calls
for
more
and
further
exploration
its
characteristics.
Methods:
Datasets
from
Gene
Expression
Omnibus
(GEO)
database
were
used
identifying
tumor
purity
DLBCL.
Survival
analysis
was
employed
analyzing
prognosis
DLBCL
patients.
Immunohistochemistry
conducted
to
detect
important
factors
that
influenced
prognosis.
Drug-sensitive
prediction
performed
evaluate
value
model.
Results:
VCAN,
CD3G,
C1QB
identified
as
three
key
genes
impacted
outcome
patients
both
in
GEO
datasets
samples
our
center.
Among
them,
VCAN
CD3G+
T
cells
correlated
with
favorable
prognosis,
worse
The
ratio
CD68
+
macrophages
CD8
associated
better
In
addition,
CD3G+T
significantly
macrophages,
CD4
cells,
+T
ratio,
indicating
it
could
play
an
role
anti-tumor
immunity
riskScore
model
constructed
based
on
RNASeq
data
C1QB,
CD3G
work
well
predicting
drug
sensitivity.
Conclusions:
DLBCL,
also
exert
certain
impact
sensitivity
Funding:
This
supported
by
Shenzhen
High-level
Hospital
Construction
Fund
CAMS
Innovation
Medical
Sciences
(CIFMS)
(2022-I2M-C&T-B-062).
Frontiers in Pharmacology,
Journal Year:
2023,
Volume and Issue:
14
Published: April 3, 2023
Introduction:
Research
has
revealed
that
the
tumor
microenvironment
(TME)
is
associated
with
progression
of
malignancy.
The
combination
meaningful
prognostic
biomarkers
related
to
TME
expected
be
a
reliable
direction
for
improving
diagnosis
and
treatment
non-small
cell
lung
cancer
(NSCLC).
Method
Result:
Therefore,
better
understand
connection
between
survival
outcomes
NSCLC,
we
used
“DESeq2”
R
package
mine
differentially
expressed
genes
(DEGs)
two
groups
NSCLC
samples
according
optimal
cutoff
value
immune
score
through
ESTIMATE
algorithm.
A
total
978
up-DEGs
828
down-DEGs
were
eventually
identified.
fifteen-gene
signature
was
established
via
LASSO
Cox
regression
analysis
further
divided
patients
into
risk
sets.
outcome
high-risk
significantly
worse
than
low-risk
in
both
TCGA
external
validation
sets
(
p-value
<
0.05).
gene
showed
high
predictive
accuracy
(1-year
area
under
time-dependent
ROC
curve
(AUC)
=
0.722,
2-year
AUC
0.708,
3-year
0.686).
nomogram
comprised
clinicopathological
information
constructed,
calibration
plots
curves
applied,
KEGG
GSEA
analyses
epithelial-mesenchymal
transition
(EMT)
pathway,
E2F
target
pathway
immune-associated
mainly
involved
group.
Further
somatic
mutation
conducted
compare
differences
groups.
Drug
sensitivity
provides
potential
basis
clinical
treatment.
Finally,
EREG
ADH1C
selected
as
key
overlapping
results
from
PPI
multiple
analyses.
They
verified
by
comparing
mRNA
expression
lines
protein
HPA
database,
confirmed
effectiveness
genes.
Conclusion:
In
conclusion,
obtained
an
immune-related
mechanism
sensitive
drugs
underling
prognosis
model,
which
may
provide
accurate
prediction
available
strategies
NSCLC.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Oct. 5, 2023
Abstract
Background
Diffuse
large
B-cell
lymphoma
(DLBCL)
is
the
predominant
type
of
malignant
lymphoma.
Although
various
treatments
have
been
developed,
limited
efficacy
calls
for
more
and
further
exploration
its
characteristics.
Methods
Datasets
from
Gene
Expression
Omnibus
(GEO)
database
were
used
identifying
tumor
purity
DLBCL.
Survival
analysis
was
employed
analyzing
prognosis
DLBCL
patients.
Immunohistochemistry
conducted
to
detect
important
factor
that
influenced
prognosis.
Drug
sensitive
prediction
performed
evaluate
value
constructed
model.
Results
VCAN,
CD3G
C1QB
identified
as
three
key
genes
impacted
outcome
patients
both
in
GEO
datasets
samples
our
center.
Among
them,
VCAN
CD3G+
T
cells
correlated
with
favorable
prognosis,
worse
The
ratio
CD68+
macrophages
CD8+
associated
better
In
addition,
significantly
macrophages,
CD4+
ratio,
indicating
it
could
play
an
role
anti-tumor
immunity
riskScore
model
based
on
RNASeq
data
work
well
predicting
drug
sensitivity.
Conclusion
DLBCL,
also
exert
certain
impact
sensitivity