Bridging the Gap in Understanding Bone Metastasis: A Multifaceted Perspective
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(5), С. 2846 - 2846
Опубликована: Фев. 29, 2024
The
treatment
of
patients
with
advanced
cancer
poses
clinical
problems
due
to
the
complications
that
arise
as
disease
progresses.
Bone
metastases
are
a
common
problem
may
face,
and
currently,
there
no
effective
drugs
treat
these
individuals.
Prostate,
breast,
lung
cancers
often
spread
bone,
causing
significant
disabling
health
conditions.
bone
is
highly
active
dynamic
tissue
considered
favorable
environment
for
growth
cancer.
role
osteoblasts
osteoclasts
in
process
remodeling
way
which
their
interactions
change
during
progression
metastasis
critical
understanding
pathophysiology
this
disease.
These
create
self-perpetuating
loop
stimulates
metastatic
cells
bone.
metabolic
reprogramming
both
microenvironment
has
serious
implications
development
metastasis.
Insight
into
systemic
elements
regulate
process,
well
cellular
changes
occur
metastases,
discovery
cure
It
crucial
explore
different
therapeutic
options
focus
specifically
on
malignancy
order
effectively
This
review
will
effects
disorders
factors
like
hormones
cytokines
metastases.
We
also
examine
various
alternatives
available
today
upcoming
advances
novel
treatments.
Язык: Английский
Cannabinoid Receptor Type 2 Agonist, GW405833, Reduced the Impacts of MDA‐MB‐231 Breast Cancer Cells on Bone Cells
Cancer Medicine,
Год журнала:
2025,
Номер
14(4)
Опубликована: Фев. 1, 2025
ABSTRACT
Aim
Breast
cancer
frequently
metastasizes
to
bones.
The
interaction
between
breast
cells
and
bone
results
in
osteolytic
lesions
by
disrupting
the
balance
osteoblast‐mediated
production
osteoclast‐mediated
resorption.
This
study
aims
investigate
effects
of
cannabinoid
receptor
type
2
(CB2)
agonist,
GW405833,
on
interactions
osteoblasts
as
well
its
impact
cancer‐induced
osteoclastogenesis.
Materials
&
Methods
MDA‐MB‐231,
UMR‐106,
RAW
264.7
were
used
represent
cells,
osteoblast‐like
macrophage‐osteoclast
precursor
respectively.
Cell
viability
was
evaluated
MTT
assay,
cell
invasion
assessed
Transwell
assay.
Tartrate‐resistant
acid
phosphatase
(TRAP)
staining
utilized
evaluate
Results
Our
demonstrated
that
GW405833
disrupted
MDA‐MB‐231‐induced
UMR‐106
death
promoted
viability.
underlying
mechanism
these
determined
this
study.
reduced
AKT
phosphorylation
MDA‐MB‐231
without
affecting
mTOR
protein
expression
or
phosphorylation.
Conversely,
induced
phosphorylated
protein.
Furthermore,
inhibitor
reversed
GW405833‐induced
recovery
under
MDA‐MB‐231‐derived
conditioned
media
(CM)
exposure.
These
findings
underscore
critical
role
AKT/mTOR
pathway
mediating
GW405833's
inhibitory
cancer‐bone
interactions.
Additionally,
suppressed
osteoblast‐enhanced
invasion‐related
proteins
both
types,
along
with
reducing
osteoclastogenic
factors
CM
suppressing
CM‐enhanced
osteoclastogenesis
cells.
Conclusion
highlights
therapeutic
potential
agonist
for
treating
metastasis
bone‐related
complications.
Язык: Английский
SPP1‐SRD5A3 signaling axis regulated lymph node metastasis by activating Mucin type O glycan biosynthesis
The FASEB Journal,
Год журнала:
2025,
Номер
39(7)
Опубликована: Апрель 2, 2025
Lymph
node
metastasis
(LNM)
holds
substantial
implications
for
the
recurrence
and
survival
of
cancer
patients,
but
intricate
regulatory
mechanisms
underlying
LNM
remain
poorly
understood.
MTOGB
was
dominantly
increased
in
pan-cancer,
significantly
activated
epithelial
cells
enriched
LNM.
Subsequently,
we
identified
a
specific
cell
subpopulation,
EC4,
located
at
terminal
differentiation
trajectory
Lineage2.
By
intersecting
differentially
expressed
genes
cluster
2,
EC4
Lineage2,
six
crucial
genes.
Notably,
expression
Steroid
5α-reductase
3
(SRD5A3)
with
progression
stages.
Knockdown
SRD5A3
effectively
suppressed
MTOGB,
blocking
both
animal
models.
Nilotinib
screened
as
candidate
inhibitor
confirmed
to
remarkably
decrease
metastasis.
SOX4
potential
transcription
factor
SRD5A3,
modulated
by
dramatic
increase
communication
SPP1+
macrophages
immune
microenvironment.
The
supernatant
from
macrophage
enhanced
SOX4/SRD5A3
metastatic
ability
cells,
this
effect
reversed
deletion
SPP1.
Collectively,
our
findings
illuminate
SPP1-SRD5A3
signaling
driver
suggest
that
its
blockade
could
be
promising
option
overcoming
Язык: Английский
Circular RNAs: Emerging regulators of signaling pathways in epithelial-mesenchymal transition and angiogenesis during breast cancer progression
Nivruthi Sasi,
Dilipkumar Preetha,
Saranya Iyyappan
и другие.
Seminars in Oncology,
Год журнала:
2025,
Номер
52(2), С. 152340 - 152340
Опубликована: Апрель 1, 2025
Язык: Английский
The signature of extracellular vesicles in hypoxic breast cancer and their therapeutic engineering
Cell Communication and Signaling,
Год журнала:
2024,
Номер
22(1)
Опубликована: Окт. 21, 2024
Abstract
Breast
cancer
(BC)
currently
ranks
second
in
the
global
incidence
rate.
Hypoxia
is
a
common
phenomenon
BC.
Under
hypoxic
conditions,
cells
tumor
microenvironment
(TME)
secrete
numerous
extracellular
vesicles
(EVs)
to
achieve
intercellular
communication
and
alter
metabolism
of
primary
metastatic
tumors
that
shape
TME.
In
addition,
emerging
studies
have
indicated
hypoxia
can
promote
resistance
treatment.
Engineered
EVs
are
expected
become
carriers
for
treatment
due
their
high
biocompatibility,
low
immunogenicity,
drug
delivery
efficiency,
ease
modification.
this
review,
we
summarize
mechanisms
TME
distant
metastasis
BC
under
conditions.
Additionally,
highlight
potential
applications
engineered
mitigating
malignant
phenotypes
hypoxia.
Язык: Английский
Exploration of marine natural compounds as promising MDM2 inhibitors for treating triple-negative breast cancer: insights from molecular docking, ADME/T studies, molecular dynamics simulation and MM-PBSA binding free energy calculations
Discover Chemistry.,
Год журнала:
2024,
Номер
1(1)
Опубликована: Ноя. 28, 2024
Triple-negative
breast
cancer
(TNBC),
the
most
aggressive
form
of
cancer,
presents
a
significant
mortality
risk
owing
to
its
elevated
potential
for
metastasis.
The
overexpression
Murine
Double
Minute
2
homolog
(MDM2)
protein,
key
suppressor
tumour
p53,
in
TNBC
amplifies
growth,
advancement,
and
invasiveness.
Thus,
inhibiting
MDM2
protein
emerges
as
compelling
strategy
enhance
efficacy
treatment.
We
aimed
identify
novel
inhibitors
from
natural
marine
compounds,
known
their
distinctive
chemical
structures
heightened
anticancer
activities,
utilizing
molecular
docking,
ADME/T
analysis,
dynamics
(MD)
simulations,
MM-PBSA
calculations,
silico
PASS
predictions.
A
compound
library
was
constructed
initial
screening
purpose
docking
analysis
revealed
that
two
namely
10,11-dihydrosodwanone
B
sodwanone
T,
exhibited
significantly
higher
binding
affinity
(−
9.6
kcal/mol
−
9.1
kcal/mol,
respectively)
compared
established
inhibitor
nutlin-3a
8.4
kcal/mol).
investigations
were
conducted
ensure
drug-likeness
properties
safety
these
compounds.
Additionally,
tool
predicted
both
compounds
possess
activities.
Molecular
simulations
(100
ns)
calculations
indicated
T
formed
relatively
more
stable
complex
had
binding-free
energy
with
MDM2,
respectively.
In
conclusion,
this
research
suggests
promising
candidate
further
testing
development
an
therapeutic
applications
against
TNBC.
Nevertheless,
substantial
experimental
clinical
are
necessary
applicability
settings.
Язык: Английский
How Schwann Cells Are Involved in Brain Metastasis
Neuroglia,
Год журнала:
2024,
Номер
5(2), С. 155 - 164
Опубликована: Июнь 1, 2024
The
current
lack
of
a
comprehensive
understanding
brain
metastasis
mechanisms
presents
significant
gap
in
cancer
research.
This
review
outlines
the
role
that
Schwann
cells
(SCs)
have
this
process.
SCs
are
already
known
for
their
myelination
and
nerve
repair
within
peripheral
nervous
system
(PNS),
but
there
is
less
information
on
function
facilitating
transport
activation
neoplastic
to
aid
invasion
blood–brain
barrier
brain.
Detailed
insights
into
SCs’
interactions
with
various
cancers,
including
lung,
breast,
melanoma,
colon,
kidney,
pancreatic
reveal
how
these
coerced
repair-like
phenotypes
accelerate
spread
modulate
immune
responses.
By
outlining
involvement
perineural
BBB
modification,
highlights
functions
metastasis.
Язык: Английский
The interplay between breast cancer and the nervous system during the progression of breast cancer and implications for its targeted therapy
Guocui Cai,
Feiyang Songa
BIO Web of Conferences,
Год журнала:
2024,
Номер
124, С. 02015 - 02015
Опубликована: Янв. 1, 2024
Breast
cancer
ranks
as
a
leading
cause
of
cancer-related
deaths
in
women
globally.
Current
treatments
often
fall
short
eradicating
it
completely,
posing
challenges
managing
its
incidence
and
mortality
rates.
The
nervous
system
significantly
influences
breast
initiation,
progression,
metastasis.
review
highlights
how
the
hypothalamic-pituitary-adrenal
axis
central
peripheral
nerves,
such
parasympathetic
sympathetic
can
either
promote
or
inhibit
development
through
neurotransmitter
release.
Understanding
these
mechanisms
offers
new
therapeutic
targets,
potentially
improving
diagnosis
treatment
strategies.
Язык: Английский
Neutrophil-targeted liposomal platform: A shift in novel approach for early detection and treatment of cancer metastasis
Asian Journal of Pharmaceutical Sciences,
Год журнала:
2024,
Номер
19(5), С. 100949 - 100949
Опубликована: Авг. 23, 2024
Tumor
metastasis
is
responsible
for
90%
of
cancer-associated
deaths,
and
its
early
detection
may
decrease
the
likelihood
mortality.
Studies
have
demonstrated
that
results
from
interaction
between
"seeds"
(tumor
cells)
"soil"
(pre-metastatic
niche,
PMN).
As
first
most
abundant
immune
cells
to
be
recruited
PMN,
neutrophils
play
a
key
role
in
ultimate
formation
metastatic
foci
through
mechanisms
such
as
supporting
tumor
cell
growth,
promoting
angiogenesis,
shaping
an
immune-suppressive
microenvironment.
In
this
study,
two
distinct
types
sialic
acid
(SA)-modified
liposomes
were
prepared
target
regulate
pro-metastatic
l-selectin
receptor.
One
these
liposomes,
named
ICG@SAL,
was
used
encapsulate
indocyanine
green
(ICG)
specifically
designed
cancer
metastasis.
The
other
liposome,
referred
ABE/Cur@SAL,
co-loaded
abemaciclib
(ABE)
curcumin
(Cur),
with
intention
suppressing
progression
tumor.
Fluorescence
imaging
mouse
spontaneous
model
indicated
ICG@SAL
faster
targeting
stronger
accumulation
organs
than
unmodified
ICG
(ICG@CL).
This
suggested
could
detect
at
stage.
therapy
experimental
lung
ABE/Cur@SAL
inhibit
regulatory
T
(Treg)
proliferation,
enhance
effector
activity
reduce
tumorigenic
factor
release,
implying
Overall,
our
work
provided
sensitive
convenient
approach
diagnosis
treatment
employed
metastasis,
while
development
when
identified.
Язык: Английский
Construction of a novel mitochondrial oxidative stress-related genes prognostic system and molecular subtype characterization for breast cancer
Discover Oncology,
Год журнала:
2024,
Номер
15(1)
Опубликована: Ноя. 8, 2024
Breast
cancer
(BRCA)
is
the
most
common
malignant
tumor
among
women,
characterized
by
high
incidence
rates
and
mortality
rates.
Oxidative
stress
immunity,
particularly
in
relation
to
mitochondria,
have
emerged
as
pivotal
factors
breast
carcinogenesis.
Nonetheless,
limited
research
has
explored
specific
contribution
of
mitochondrial
oxidative
prognosis
BRCA.
Язык: Английский