Discover Oncology,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Nov. 13, 2024
The
microenvironment
of
clear
cell
renal
carcinoma
(ccRCC)
is
characterized
by
hypoxia
and
increased
lactate
production.
However,
the
impact
metabolism
on
ccRCC
remains
incompletely
understood.
In
this
study,
a
new
molecular
subtype
developed
based
hypoxia-related
genes
(HRGs)
metabolism-related
(LMRGs),
aiming
to
create
tool
that
can
predict
survival
rate,
immune
status,
responsiveness
treatment
patients.
We
obtained
RNA-seq
data
clinical
information
patients
with
from
TCGA
GEO.
HRGs
LMRGs
are
sourced
Molecular
Signatures
Database.
Integrating
10
machine
learning
algorithms
101
frameworks,
we
constructed
prognostic
model
related
metabolism.
Its
accuracy
reliability
evaluated
through
constructing
nomograms,
drawing
ROC
curves,
validating
datasets.
Additionally,
risk
subgroups
functional
enrichment,
tumor
mutational
burden
(TMB),
infiltration
degree,
checkpoint
expression
level.
Finally,
evaluate
immunotherapy
determine
personalized
drugs
for
specific
subgroups.
85
valuable
were
screened
out.
Functional
enrichment
analysis
shows
group
high-risk
scores
(HLMRGS)
mainly
involved
in
activation
immune-related
activities,
while
low
HLMRGS
more
active
metabolic
tumor-related
pathways.
At
same
time,
differences
cellular
states
between
high
observed.
potential
determined.
have
novel
signature
integrates
It
expected
become
an
effective
prognosis
prediction,
medicine
ccRCC.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 12, 2024
Background:
Tumor
heterogeneity
is
associated
with
poor
prognosis
and
drug
resistance,
leading
to
therapeutic
failure.
Here,
we
aim
utilize
tumor
evolution
analysis
decode
the
intra-
inter-tumoral
of
high-grade
serous
ovarian
cancer
(HGSOC),
unraveling
correlation
between
as
well
chemotherapy
response
through
single-cell
spatial
transcriptomic
analysis.
Methods:
We
collected
curated
28
HGSOC
patients
data
from
five
datasets.
Then,
developed
a
novel
text
mining-based
machine
learning
approach
deconstruct
evolutionary
patterns
cell
functions.
This
allowed
us
identify
key
tumor-related
genes
within
different
branches,
elucidate
microenvironmental
compositions
that
various
functional
cells
depend
on,
analyze
inter-heterogeneity
tumors
their
microenvironments
in
relation
patients.
further
validated
our
findings
two
seven
bulk
datasets,
totally
1,030
Results:
By
employing
clusters
proxies
for
clonality,
identified
significant
increase
state
heterogeneity,
which
was
strongly
correlated
patient
treatment
response.
Furthermore,
increased
clonality
characteristics
cancer-associated
fibroblast
(CAF).
also
found
proximity
CXCL12-positive
CAF
cells,
mediated
CXCL12/CXCR4
interaction,
highly
positively
resistance
HGSOC.
Finally,
constructed
panel
24
statistical
modeling,
are
fibroblasts
can
predict
both
Conclusions:
Our
study
offers
insights
into
collective
behavior
communities
HGSOC,
potential
drivers
therapy.
Functional
analyses
experiments
revealed
strong
association
progression
outcomes.
provide
an
important
theoretical
basis
clinical
treatment.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 5, 2024
Abstract
Tumor
heterogeneity
is
associated
with
poor
prognosis
and
drug
resistance,
leading
to
therapeutic
failure.
Here,
we
used
tumor
evolution
analysis
determine
the
intra-
intertumoral
of
high-grade
serous
ovarian
cancer
(HGSOC)
analyze
correlation
between
prognosis,
as
well
chemotherapy
response,
through
single-cell
spatial
transcriptomic
analysis.
We
collected
curated
28
HGSOC
patients’
data
from
five
datasets.
Then,
developed
a
novel
text-mining-based
machine-learning
approach
deconstruct
evolutionary
patterns
cell
functions.
then
identified
key
tumor-related
genes
within
different
branches,
characterized
microenvironmental
compositions
that
various
functional
cells
depend
on,
analyzed
microenvironments.
These
analyses
were
conducted
in
relation
response
patients.
validated
our
findings
two
seven
bulk
datasets
(total:
1,030
patients).
Using
clusters
proxies
for
clonality,
significant
increase
state
was
strongly
correlated
patient
treatment
response.
Furthermore,
increased
clonality
characteristics
cancer-associated
fibroblasts
(CAFs).
The
proximity
CXCL12-positive
CAFs
cells,
mediated
CXCL12/CXCR4
interaction,
highly
positively
resistance
HGSOC.
In
this
study,
constructed
panel
24
statistical
modeling
correlate
can
predict
both
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: Nov. 4, 2024
Tumor
heterogeneity
is
associated
with
poor
prognosis
and
drug
resistance,
leading
to
therapeutic
failure.
Here,
we
used
tumor
evolution
analysis
determine
the
intra-
intertumoral
of
high-grade
serous
ovarian
cancer
(HGSOC)
analyze
correlation
between
prognosis,
as
well
chemotherapy
response,
through
single-cell
spatial
transcriptomic
analysis.
We
collected
curated
28
HGSOC
patients'
data
from
five
datasets.
Then,
developed
a
novel
text-mining-based
machine-learning
approach
deconstruct
evolutionary
patterns
cell
functions.
then
identified
key
tumor-related
genes
within
different
branches,
characterized
microenvironmental
compositions
that
various
functional
cells
depend
on,
analyzed
microenvironments.
These
analyses
were
conducted
in
relation
response
patients.
validated
our
findings
two
seven
bulk
datasets
(total:
1,030
patients).
Using
clusters
proxies
for
clonality,
significant
increase
state
was
strongly
correlated
patient
treatment
response.
Furthermore,
increased
clonality
characteristics
cancer-associated
fibroblasts
(CAFs).
The
proximity
CXCL12-positive
CAFs
cells,
mediated
CXCL12/CXCR4
interaction,
highly
positively
resistance
HGSOC.
Finally,
constructed
panel
24
statistical
modeling
correlate
can
predict
both
Our
study
offers
insights
into
collective
behavior
communities
HGSOC,
potential
drivers
therapy.
There
strong
association
progression,
outcomes.
Discover Oncology,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Nov. 13, 2024
The
microenvironment
of
clear
cell
renal
carcinoma
(ccRCC)
is
characterized
by
hypoxia
and
increased
lactate
production.
However,
the
impact
metabolism
on
ccRCC
remains
incompletely
understood.
In
this
study,
a
new
molecular
subtype
developed
based
hypoxia-related
genes
(HRGs)
metabolism-related
(LMRGs),
aiming
to
create
tool
that
can
predict
survival
rate,
immune
status,
responsiveness
treatment
patients.
We
obtained
RNA-seq
data
clinical
information
patients
with
from
TCGA
GEO.
HRGs
LMRGs
are
sourced
Molecular
Signatures
Database.
Integrating
10
machine
learning
algorithms
101
frameworks,
we
constructed
prognostic
model
related
metabolism.
Its
accuracy
reliability
evaluated
through
constructing
nomograms,
drawing
ROC
curves,
validating
datasets.
Additionally,
risk
subgroups
functional
enrichment,
tumor
mutational
burden
(TMB),
infiltration
degree,
checkpoint
expression
level.
Finally,
evaluate
immunotherapy
determine
personalized
drugs
for
specific
subgroups.
85
valuable
were
screened
out.
Functional
enrichment
analysis
shows
group
high-risk
scores
(HLMRGS)
mainly
involved
in
activation
immune-related
activities,
while
low
HLMRGS
more
active
metabolic
tumor-related
pathways.
At
same
time,
differences
cellular
states
between
high
observed.
potential
determined.
have
novel
signature
integrates
It
expected
become
an
effective
prognosis
prediction,
medicine
ccRCC.