Journal of Cellular and Molecular Medicine,
Год журнала:
2024,
Номер
28(23)
Опубликована: Дек. 1, 2024
ABSTRACT
Prostate
cancer
(PCa)
constitutes
a
highly
common
and
lethal
disease
that
impacts
males
globally.
However,
the
specific
molecular
pathways
responsible
for
its
development
are
still
unknown.
Therefore,
revealing
regulators
contributed
to
progression
of
PCa
is
pivotal
developing
unique
management
strategies.
Through
comprehensive
bioinformatics
analysis
multiple
public
gene
databases,
we
thoroughly
investigated
COL10A1
expression
level,
clinical
significance,
co‐expressed
genes
signalling
in
PCa.
INHBA
level
was
assessed
specimens
using
RT‐qPCR,
Western
blotting
immunohistochemistry.
A
combination
experimental
techniques,
including
CCK‐8
assay,
colony
formation,
flow
cytometry,
Transwell,
wound‐healing,
immunoprecipitation
assays
rescue
study,
utilised
examine
fundamental
COL10A1's
action
across
The
significantly
elevated
PCa,
upregulation
has
been
connected
with
tumour
aggressiveness
weak
predictive
outcome
subjects.
current
investigation
revealed
regulation
expression,
either
by
or
downregulation,
resulted
sequential
augmentation
suppression
cell
progression,
migration
invasion.
Mechanistically,
manifested
directly
interact
facilitate
PI3K
AKT
phosphorylation
within
cells
mouse
models.
results
our
study
offer
new
perspectives
on
tumorigenic
role
interactions
may
play
important
roles
progression.
Research Square (Research Square),
Год журнала:
2024,
Номер
unknown
Опубликована: Май 30, 2024
Abstract
Cervical
cancer
ranks
as
the
fourth
most
prevalent
among
women
globally,
and
in
recent
years,
there
has
been
widespread
attention
on
role
of
lipids
tumorigenesis
development.
This
study
utilized
Mendelian
Randomization
(MR)
to
explore
causal
relationship
between
immune
cell-mediated
cervical
risk.
We
have
selected
lipids,
which
are
closely
associated
with
function
cells,
identified
their
genetic
instrumental
variables.
Using
large-scale
genomic
association
(GWAS)
data,
we
genetically
evaluated
levels
analyzed
correlation
risk
Preliminary
results
suggest
that
triacylglycerol
is
significantly
And
elevated
an
increased
cancer.
In
addition,
found
regulatory
cells
such
BAFF
−
R
naive
mature
B
cell,
IgD+,
transitional
may
indirectly
influence
development
by
influencing
response.
Our
research,
employing
inference
analysis
randomization,
demonstrates
significance
cell-induced
progression.
These
contribute
comprehending
origins
might
steer
creation
upcoming
preventive
approaches
therapeutic
tactics.
Additional
studies
essential
confirm
these
investigate
particular
biological
processes.
Research Square (Research Square),
Год журнала:
2024,
Номер
unknown
Опубликована: Июнь 5, 2024
Abstract
Cervical
cancer
ranks
as
the
fourth
most
prevalent
among
women
globally,
and
in
recent
years,
there
has
been
widespread
attention
on
role
of
lipids
tumorigenesis
development.
This
study
utilized
Mendelian
Randomization
(MR)
to
explore
causal
relationship
between
immune
cell-mediated
cervical
risk.
We
have
selected
lipids,
which
are
closely
associated
with
function
cells,
identified
their
genetic
instrumental
variables.
Using
large-scale
genomic
association
(GWAS)
data,
we
genetically
evaluated
levels
analyzed
correlation
risk
Preliminary
results
suggest
that
triacylglycerol
is
significantly
And
elevated
an
increased
cancer.
In
addition,
found
regulatory
cells
such
BAFF
−
R
naive
mature
B
cell,
IgD+,
transitional
may
indirectly
influence
development
by
influencing
response.
Our
research,
employing
inference
analysis
randomization,
demonstrates
significance
cell-induced
progression.
These
contribute
comprehending
origins
might
steer
creation
upcoming
preventive
approaches
therapeutic
tactics.
Additional
studies
essential
confirm
these
investigate
particular
biological
processes.
Chemical Biology & Drug Design,
Год журнала:
2024,
Номер
103(6)
Опубликована: Июнь 1, 2024
Abstract
Docetaxel
(DTX)
resistance
poses
a
significant
challenge
in
the
treatment
of
prostate
cancer
(PCa),
often
leading
to
chemotherapy
failure.
This
study
investigates
ability
piperine,
compound
derived
from
black
pepper,
enhance
sensitivity
PCa
cells
DTX
and
elucidates
its
underlying
mechanism.
We
established
DTX‐resistant
cell
line,
DU145/DTX,
conduct
our
experiments.
Through
series
assays,
including
MTT
for
viability,
flow
cytometry
apoptosis,
Transwell
migration
invasion,
western
blot
protein
expression
analysis,
we
assessed
effects
piperine
on
these
cellular
functions
Notch
signaling
pathway
components.
Our
results
demonstrated
that
successfully
line
DU145/DTX.
Piperine
effectively
decreased
viability
both
DU145
counterpart,
concentration
time‐dependent
manner
when
used
alone
combination
with
DTX.
Notably,
also
induced
apoptosis
reduced
invasion
capabilities
cells.
At
molecular
level,
down‐regulated
by
inhibiting
Notch1
Jagged1
signaling,
as
well
reducing
downstream
effectors
Hey1
hes
family
bHLH
transcription
factor
1.
The
concludes
piperine's
modulate
induce
highlights
potential
complementary
PCa,
paving
way
use
traditional
Chinese
medicinal
compounds
modern
oncology
strategies.
Frontiers in Pharmacology,
Год журнала:
2024,
Номер
15
Опубликована: Сен. 17, 2024
Background
The
role
of
focal
amplifications
and
extrachromosomal
circular
DNA
(eccDNA)
is
still
uncertain
in
prostate
adenocarcinoma
(PRAD).
Here,
we
first
mapped
the
global
characterizations
eccDNA
then
investigate
characterization
eccDNA-amplified
key
differentially
expressed
encoded
genes
(eKDEGs)
progression,
immune
response
immunotherapy
PRAD.
Methods
Circular_seq
was
used
conjunction
with
TCGA-PRAD
transcriptome
dataset
to
sequence,
annotate,
filter
for
coding
(eDEGs)
PRAD
para-cancerous
normal
tissues.
Afterwards,
risk
models
were
created
eKDEGs
linked
prognosis
identified
using
Cox
Lasso
regression
analysis.
microenvironment
model
quantified
a
variety
immunological
algorithms,
which
also
its
characteristics
regard
immunotherapy,
response,
infiltration.
Results
In
this
research,
there
no
significant
difference
size,
type,
chromosomal
distribution
However,
4,290
eccDNAs
1,981
amplified.
Following
that,
499
eDEGs
tested
from
TCGA-PRAD.
By
techniques,
ZNF330
PITPNM3
as
PRAD,
new
conducted
based
on
this.
Survival
analysis
showed
that
high-risk
group
associated
poor
validated
external
data.
Immune
infiltration
risks
affected
cell
not
only
mediating
changes
function,
but
correlating
immunophenotyping.
Furthermore,
negatively
anti-
CTLA-4
/anti-
PD-1
mutational
burden.
addition,
Tumor
Dysfunction
Exclusion
analyses
more
prone
escape.
Drug
sensitivity
10
drugs,
instructive
treatment.
Conclusion
PITPNM
are
can
be
potential
prognostic
markers.
two-factor
combined
effectively
assess
survival
patients,
predict
different
responses
may
provide
ideas
immunotherapy.
Turkish Journal of Biochemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 5, 2024
Abstract
Background
Prostate
cancer
is
the
most
frequently
diagnosed
male
and
fifth
highest
cause
of
mortality
in
men.
CDR1as
has
played
an
essential
role
growth
several
malignancies.
However,
its
significance
progression
prostate
not
been
investigated.
We
aimed
to
investigate
mechanism
development
identify
a
new
target
for
diagnostics
treatment.
Methods
siRNA
miR-7-5p
mimic
were
transfected
into
PC3
DU145
PCa
cell
lines
their
effects
on
cellular
processes
Cell
viability
was
measured
by
WST-8
assay.
The
and/or
migration
detected
using
scratch-wound
apoptotic
capacity
cells
evaluated
Caspase-3
kit.
potential
targets
defined
via
silico
tools.
mRNA
protein
expression
levels
IGF1R
EIF4E
qRT-PCR
western
blot
assays,
respectively.
matching
between
luciferase
reporter
Results
Inhibiting
or
restoring
reduced
proliferation
while
increasing
apoptosis.
Silencing
elevated
decreasing
IGF1R.
Conclusions
functions
as
sponge,
promoting
tumor
development.
Journal of Cellular and Molecular Medicine,
Год журнала:
2024,
Номер
28(23)
Опубликована: Дек. 1, 2024
ABSTRACT
Prostate
cancer
(PCa)
constitutes
a
highly
common
and
lethal
disease
that
impacts
males
globally.
However,
the
specific
molecular
pathways
responsible
for
its
development
are
still
unknown.
Therefore,
revealing
regulators
contributed
to
progression
of
PCa
is
pivotal
developing
unique
management
strategies.
Through
comprehensive
bioinformatics
analysis
multiple
public
gene
databases,
we
thoroughly
investigated
COL10A1
expression
level,
clinical
significance,
co‐expressed
genes
signalling
in
PCa.
INHBA
level
was
assessed
specimens
using
RT‐qPCR,
Western
blotting
immunohistochemistry.
A
combination
experimental
techniques,
including
CCK‐8
assay,
colony
formation,
flow
cytometry,
Transwell,
wound‐healing,
immunoprecipitation
assays
rescue
study,
utilised
examine
fundamental
COL10A1's
action
across
The
significantly
elevated
PCa,
upregulation
has
been
connected
with
tumour
aggressiveness
weak
predictive
outcome
subjects.
current
investigation
revealed
regulation
expression,
either
by
or
downregulation,
resulted
sequential
augmentation
suppression
cell
progression,
migration
invasion.
Mechanistically,
manifested
directly
interact
facilitate
PI3K
AKT
phosphorylation
within
cells
mouse
models.
results
our
study
offer
new
perspectives
on
tumorigenic
role
interactions
may
play
important
roles
progression.