Translational Cancer Research,
Journal Year:
2024,
Volume and Issue:
13(11), P. 5725 - 5750
Published: Nov. 1, 2024
Head
and
neck
squamous
cell
carcinoma
(HNSCC)
contributes
significantly
to
global
health
challenges,
presenting
primarily
in
the
oral
cavity,
pharynx,
nasopharynx,
larynx.
HNSCC
has
a
high
propensity
for
lymphatic
metastasis.
Diffuse
large
B-cell
lymphoma
(DLBCL),
most
common
subtype
of
non-Hodgkin
lymphoma,
exhibits
significant
heterogeneity
aggressive
behavior,
leading
mortality
rates.
Epstein-Barr
virus
(EBV)
is
notably
associated
with
DLBCL
certain
types
HNSCC.
The
purpose
this
study
elucidate
molecular
immune
interplay
between
using
bioinformatics
machine
learning
(ML)
identify
shared
biomarkers
potential
therapeutic
targets.
Differentially
expressed
genes
(DEGs)
were
identified
"limma"
package
R
from
dataset
Cancer
Genome
Atlas
(TCGA)
database,
relevant
modules
selected
through
weighted
gene
co-expression
network
analysis
(WGCNA)
Gene
Expression
Omnibus
(GEO)
database.
Based
on
their
intersection
genes,
functional
enrichment
analyses
conducted
Ontology
(GO),
Disease
Ontology,
Kyoto
Encyclopedia
Genes
Genomes
(KEGG)
databases.
Protein-protein
interaction
(PPI)
networks
ML
algorithms
employed
screen
biomarkers.
prognostic
value
these
was
evaluated
Kaplan-Meier
(K-M)
survival
receiver
operating
characteristic
(ROC)
curve
analyses.
Human
Protein
(HPA)
database
facilitated
examination
messenger
RNA
(mRNA)
protein
expressions.
Further
mutations,
infiltration,
drug
predictions,
pan-cancer
impacts
performed.
Additionally,
single-cell
sequencing
(scRNA-seq)
data
at
type
level
provide
deeper
insights
into
tumor
microenvironment.
From
2,040
DEGs
1,983
module-related
85
identified.
PPI
six
proposed
21
prospective
followed
yielded
16
candidates.
Survival
ROC
pinpointed
four
hub
genes-ACACB,
MMP8,
PAX5,
TNFAIP6-as
patient
outcomes,
demonstrating
predictive
capabilities.
Evaluations
mutations
coupled
prediction
comprehensive
cancer
analysis,
highlighted
biomarkers'
roles
response
treatment
efficacy.
scRNA-seq
revealed
an
increased
abundance
fibroblasts,
epithelial
cells
mononuclear
phagocyte
system
(MPs)
tissues
compared
lymphoid
tissues.
MMP8
showed
higher
expression
five
tissues,
while
TNFAIP6
PAX5
exhibited
specific
types.
Leveraging
ML,
pivotal
diagnostic
capabilities
corroborates
accuracy,
supporting
development
nomogram
assist
clinical
decision-making.
Frontiers in Oncology,
Journal Year:
2024,
Volume and Issue:
14
Published: May 2, 2024
To
investigate
the
correlation
between
programmed
death
ligand
1(PD-L1),
tumor
mutation
burden
(TMB)
and
short-term
efficacy
clinical
characteristics
of
anti-PD-1
immune
checkpoint
inhibitor
combination
chemotherapy
in
NSCLC
patients.
The
prediction
model
was
evaluated.
Seminars in Liver Disease,
Journal Year:
2024,
Volume and Issue:
44(02), P. 133 - 146
Published: May 1, 2024
Primary
liver
cancer
is
a
solid
malignancy
with
high
mortality
rate.
The
success
of
immunotherapy
has
shown
great
promise
in
improving
patient
care
and
highlights
crucial
need
to
understand
the
complexity
tumor
immune
microenvironment
(TIME).
Recent
advances
single-cell
spatial
omics
technologies,
coupled
development
systems
biology
approaches,
are
rapidly
transforming
landscape
immunology.
Here
we
review
cellular
TIME
from
perspectives.
We
also
discuss
interaction
networks
within
cell
community
regulating
responses.
further
highlight
challenges
opportunities
implications
for
biomarker
discovery,
stratification,
combination
immunotherapies.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Sept. 26, 2024
Background
Existing
epidemiological
data
indicated
a
correlation
between
thyroid
cancer
(THCA)
and
the
risk
of
secondary
primary
malignancies
(SPMs).
However,
does
not
always
imply
causality.
Methods
The
Mendelian
randomization
(MR)
analyses
were
performed
to
investigate
causal
relationships
THCA
SPMs
based
on
international
multicenter
data.
Odds
ratios
(ORs)
with
95%
confidence
intervals
(95%
CIs)
calculated.
Cancer
Genome
Atlas
(TCGA)
was
used
explore
potential
mechanisms
shared
by
bladder
(BLCA).
Results
Summary
datasets
genome-wide
association
studies
(GWAS)
30
types
cancers
obtained
from
United
Kingdom
Biobank
(UKB)
FinnGen
database.
Meta-analysis
UKB
results
revealed
that
significantly
positively
correlated
BLCA
(OR
=
1.140;
CI,
1.072-1.212;
P
<
0.001).
Four
genes,
including
WNT3,
FAM171A2,
MLLT11,
ULBP1,
identified
as
key
genes
both
TCHA
BLCA.
Correlation
analysis
may
increase
through
augmentation
N2
neutrophil
infiltration.
Conclusions
This
study
showed
causally
related
It
is
recommended
conduct
more
rigorous
screenings
for
during
follow-up
patients.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Nov. 8, 2024
Osteosarcoma,
a
highly
aggressive
malignant
bone
tumor,
is
significantly
influenced
by
the
intricate
interactions
within
its
tumor
microenvironment
(TME),
particularly
involving
neutrophils.
This
review
delineates
multifaceted
roles
of
neutrophils,
including
tumor-associated
neutrophils
(TANs)
and
neutrophil
extracellular
traps
(NETs),
in
osteosarcoma’s
pathogenesis.
TANs
exhibit
both
pro-
anti-tumor
phenotypes,
modulating
growth
immune
evasion,
while
NETs
facilitate
cell
adhesion,
migration,
immunosuppression.
Clinically,
neutrophil-related
markers
such
as
neutrophil-to-lymphocyte
ratio
(NLR)
predict
patient
outcomes,
highlighting
potential
for
neutrophil-targeted
therapies.
Unraveling
these
complex
crucial
developing
novel
treatment
strategies
that
harness
TME
to
improve
osteosarcoma
management.
Translational Cancer Research,
Journal Year:
2024,
Volume and Issue:
13(11), P. 5725 - 5750
Published: Nov. 1, 2024
Head
and
neck
squamous
cell
carcinoma
(HNSCC)
contributes
significantly
to
global
health
challenges,
presenting
primarily
in
the
oral
cavity,
pharynx,
nasopharynx,
larynx.
HNSCC
has
a
high
propensity
for
lymphatic
metastasis.
Diffuse
large
B-cell
lymphoma
(DLBCL),
most
common
subtype
of
non-Hodgkin
lymphoma,
exhibits
significant
heterogeneity
aggressive
behavior,
leading
mortality
rates.
Epstein-Barr
virus
(EBV)
is
notably
associated
with
DLBCL
certain
types
HNSCC.
The
purpose
this
study
elucidate
molecular
immune
interplay
between
using
bioinformatics
machine
learning
(ML)
identify
shared
biomarkers
potential
therapeutic
targets.
Differentially
expressed
genes
(DEGs)
were
identified
"limma"
package
R
from
dataset
Cancer
Genome
Atlas
(TCGA)
database,
relevant
modules
selected
through
weighted
gene
co-expression
network
analysis
(WGCNA)
Gene
Expression
Omnibus
(GEO)
database.
Based
on
their
intersection
genes,
functional
enrichment
analyses
conducted
Ontology
(GO),
Disease
Ontology,
Kyoto
Encyclopedia
Genes
Genomes
(KEGG)
databases.
Protein-protein
interaction
(PPI)
networks
ML
algorithms
employed
screen
biomarkers.
prognostic
value
these
was
evaluated
Kaplan-Meier
(K-M)
survival
receiver
operating
characteristic
(ROC)
curve
analyses.
Human
Protein
(HPA)
database
facilitated
examination
messenger
RNA
(mRNA)
protein
expressions.
Further
mutations,
infiltration,
drug
predictions,
pan-cancer
impacts
performed.
Additionally,
single-cell
sequencing
(scRNA-seq)
data
at
type
level
provide
deeper
insights
into
tumor
microenvironment.
From
2,040
DEGs
1,983
module-related
85
identified.
PPI
six
proposed
21
prospective
followed
yielded
16
candidates.
Survival
ROC
pinpointed
four
hub
genes-ACACB,
MMP8,
PAX5,
TNFAIP6-as
patient
outcomes,
demonstrating
predictive
capabilities.
Evaluations
mutations
coupled
prediction
comprehensive
cancer
analysis,
highlighted
biomarkers'
roles
response
treatment
efficacy.
scRNA-seq
revealed
an
increased
abundance
fibroblasts,
epithelial
cells
mononuclear
phagocyte
system
(MPs)
tissues
compared
lymphoid
tissues.
MMP8
showed
higher
expression
five
tissues,
while
TNFAIP6
PAX5
exhibited
specific
types.
Leveraging
ML,
pivotal
diagnostic
capabilities
corroborates
accuracy,
supporting
development
nomogram
assist
clinical
decision-making.