British Journal of Cancer,
Journal Year:
2024,
Volume and Issue:
131(5), P. 870 - 882
Published: July 12, 2024
Abstract
Background
The
prognostic
and
therapeutic
implications
of
endothelial
cells
(ECs)
heterogeneity
in
prostate
cancer
(PCa)
are
poorly
understood.
Methods
We
investigated
associations
EC
with
PCa
recurrence
castration
resistance
8
bulk
transcriptomic
4
single-cell
RNA-seq
cohorts.
A
recurrence-associated
(RAEC)
signature
was
constructed
by
comparing
11
machine
learning
algorithms
through
nested
cross-validation.
Functional
relevances
RAEC-specific
genes
were
also
tested.
Results
subset
ECs
significantly
associated
primary
named
RAECs.
RAECs
characteristic
tip
immature
enriched
migration,
angiogenesis,
collagen-related
pathways.
then
developed
an
18-gene
RAEC
(RAECsig)
representative
Higher
RAECsig
scores
independently
predicted
tumor
performed
better
or
comparably
compared
to
clinicopathological
factors
commercial
gene
signatures
multiple
Of
the
18
genes,
FSCN1
upregulated
from
higher
Gleason
scores;
silencing
FSCN1,
TMEME255B,
GABRD
either
attenuated
tube
formation
inhibited
cell
proliferation.
Finally,
both
castration-resistant
PCa.
Conclusion
This
study
establishes
that
links
a
resistance.
Frontiers in Oncology,
Journal Year:
2023,
Volume and Issue:
13
Published: Sept. 8, 2023
Single-cell
RNA
sequencing
(scRNA-seq)
is
a
cutting-edge
technology
that
provides
insights
at
the
individual
cell
level.
In
contrast
to
traditional
bulk
RNA-seq,
which
captures
gene
expression
an
average
level
and
may
overlook
important
details,
scRNA-seq
examines
each
as
fundamental
unit
particularly
well-suited
for
identifying
rare
populations.
Analogous
microscope
distinguishes
various
types
within
tissue
sample,
unravels
heterogeneity
diversity
single
species,
offering
great
potential
leading
method
in
future.
context
of
prostate
cancer
(PCa),
disease
characterized
by
significant
multiple
stages
progression,
emerges
powerful
tool
uncovering
its
intricate
secrets.
MedComm – Oncology,
Journal Year:
2023,
Volume and Issue:
2(3)
Published: Sept. 1, 2023
Abstract
Lymphocyte
Antigen
96
(LY96)
was
identified
as
an
oncogene
in
several
tumors.
However,
its
role
renal
cancer
has
not
been
explored.
In
the
study,
LY96
is
abnormally
expressed
using
public
kidney
sequencing
data.
The
expression
level
of
validated
paired
clinical
samples.
Survival
analyses
and
ROC
curves
are
used
to
examine
prognostic
diagnostic
value.
Gene
sets
enrichment
(GSEA)
show
might
influence
immune
processes.
Then
infiltration
results
suggest
that
positively
correlated
with
M2
macrophages
RCC.
Single‐cell
data
verify
association
macrophages.
Moreover,
various
scores
affect
efficacy
immunotherapy.
Drug
screening
be
target
vemurafenib
etoposide.
Further
experiments
confirm
spatial
co‐localization
M2,
knocking
down
can
inhibit
polarization.
Cell
viability
indicate
would
result
a
decrease
resistance
study
shows
could
act
unfavorable
biomarker
for
RCC
possibly
contribute
progression
by
promoting
macrophage.
novel
therapeutic
Prostate
cancer
(PC)
is
a
common
malignancy
of
elderly
men,
characterized
by
great
heterogeneity
in
its
clinical
course,
ranging
from
an
indolent
to
highly
aggressive
disease.
The
variant
prostate
(AVPC)
clinically
shows
atypical
pattern
disease
progression,
similar
that
small
cell
PC
(SCPC),
and
also
shares
the
chemo-responsiveness
SCPC.
term
AVPC
does
not
describe
specific
histologic
subtype
but
rather
group
tumors
that,
irrespective
morphology,
show
dictated
androgen
receptor
(AR)
indifference.
AR
indifference
represents
adaptive
response
deprivation
therapy
(ADT),
driven
epithelial
plasticity,
inherent
ability
tumor
cells
adapt
their
environment
changing
phenotypic
characteristics
bi-directional
way.
molecular
profile
entails
combined
alterations
suppressor
genes
retinoblastoma
protein
1
(RB1),
53
(TP53)
phosphatase
tensin
homolog
(PTEN).
understanding
biologic
castration-resistant
(CRPC)
need
identify
subset
patients
would
potentially
benefit
therapies
necessitate
development
prognostic
predictive
biomarkers.
This
review
aims
discuss
possible
pathophysiologic
mechanisms
potential
use
emerging
tissue-based
biomarkers
practice.
Cells,
Journal Year:
2024,
Volume and Issue:
13(4), P. 350 - 350
Published: Feb. 17, 2024
The
classification
of
tumors
into
subtypes,
characterized
by
phenotypes
determined
specific
differentiation
pathways,
aids
diagnosis
and
directs
therapy
towards
targeted
approaches.
However,
with
the
advent
explosion
next-generation
sequencing,
cancer
are
turning
out
to
be
far
more
heterogenous
than
initially
thought,
is
continually
being
updated
include
subtypes.
Tumors
indeed
highly
dynamic,
they
can
evolve
undergo
various
changes
in
their
characteristics
during
disease
progression.
picture
becomes
even
complex
when
tumor
responds
a
therapy.
In
all
these
cases,
cells
acquire
ability
transdifferentiate,
changing
subtype,
adapt
microenvironments.
These
modifications
affect
tumor’s
growth
rate,
invasiveness,
response
treatment,
overall
clinical
behavior.
Studying
subtype
transitions
crucial
for
understanding
evolution,
predicting
outcomes,
developing
personalized
treatment
strategies.
We
discuss
this
emerging
hallmark
molecular
mechanisms
involved
at
crossroads
between
microenvironment,
focusing
on
four
different
human
cancers
which
tissue
plasticity
causes
switch:
breast
cancer,
prostate
glioblastoma,
pancreatic
adenocarcinoma.
British Journal of Cancer,
Journal Year:
2024,
Volume and Issue:
131(5), P. 870 - 882
Published: July 12, 2024
Abstract
Background
The
prognostic
and
therapeutic
implications
of
endothelial
cells
(ECs)
heterogeneity
in
prostate
cancer
(PCa)
are
poorly
understood.
Methods
We
investigated
associations
EC
with
PCa
recurrence
castration
resistance
8
bulk
transcriptomic
4
single-cell
RNA-seq
cohorts.
A
recurrence-associated
(RAEC)
signature
was
constructed
by
comparing
11
machine
learning
algorithms
through
nested
cross-validation.
Functional
relevances
RAEC-specific
genes
were
also
tested.
Results
subset
ECs
significantly
associated
primary
named
RAECs.
RAECs
characteristic
tip
immature
enriched
migration,
angiogenesis,
collagen-related
pathways.
then
developed
an
18-gene
RAEC
(RAECsig)
representative
Higher
RAECsig
scores
independently
predicted
tumor
performed
better
or
comparably
compared
to
clinicopathological
factors
commercial
gene
signatures
multiple
Of
the
18
genes,
FSCN1
upregulated
from
higher
Gleason
scores;
silencing
FSCN1,
TMEME255B,
GABRD
either
attenuated
tube
formation
inhibited
cell
proliferation.
Finally,
both
castration-resistant
PCa.
Conclusion
This
study
establishes
that
links
a
resistance.