Research Square (Research Square),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Oct. 30, 2023
Abstract
Aim
Bufalin,
a
cardiotonic
steroid
derived
from
Chinese
toad
venom,
exhibits
anticancer
effects
against
variety
of
malignancies.
However,
its
mechanism
action
in
human
liver
cancer
remains
elusive.
This
study
aimed
to
elucidate
the
molecular
underpinnings
bufalin's
antitumor
activity
HepG2
hepatocellular
carcinoma
(HCC)
cells
vitro.
Methods
were
exposed
40nM
bufalin
or
0nM
as
control,
and
their
transcriptomes
compared
using
RNA
sequencing.
Differentially
expressed
genes
(DEGs)
identified
annotated,
enriched
pathways
analyzed
Gene
ontology,
Kyoto
Encyclopedia
Genes,
set
enrichment
analysis,
Genomes
databases.
Results
sequencing
revealed
771
DEGs,
comprising
362
upregulated
409
downregulated
genes.
These
DEGs
involved
78
classical
pathways,
including
18
closely
associated
with
cancer,
such
central
carbon
metabolism
cell
cycle,
DNA
replication,
fatty
acid
metabolism,
ferroptosis,
so
forth.
Eleven
(Acyl-CoA
oxidase
2
et
al.)
HCC
validated
by
quantitative
real-time
reverse
transcription-polymerase
chain
reaction,
confirming
differential
expressions
response
treatment.
Conclusions
demonstrated
that
modulates
expression
implicated
various
aspects
pathogenesis
progression,
energy
proliferation,
lipid
oxidation,
death.
findings
suggest
may
exert
effect
on
targeting
multiple
mechanisms,
provide
potential
targets
for
bufalin-based
therapy.
Molecules,
Journal Year:
2023,
Volume and Issue:
28(5), P. 2231 - 2231
Published: Feb. 27, 2023
The
renaissance
of
research
into
natural
products
has
unequivocally
and
paradigmatically
shifted
our
knowledge
about
the
significant
role
in
cancer
chemoprevention.
Bufalin
is
a
pharmacologically
active
molecule
isolated
from
skin
toad
Bufo
gargarizans
or
melanostictus.
characteristically
unique
properties
to
regulate
multiple
molecular
targets
can
be
used
harness
multi-targeted
therapeutic
regimes
against
different
cancers.
There
burgeoning
evidence
related
functional
roles
signaling
cascades
carcinogenesis
metastasis.
been
reported
pleiotropically
myriad
signal
transduction
various
Importantly,
bufalin
mechanistically
regulated
JAK/STAT,
Wnt/β-Catenin,
mTOR,
TRAIL/TRAIL-R,
EGFR,
c-MET
pathways.
Furthermore,
bufalin-mediated
modulation
non-coding
RNAs
cancers
also
started
gain
tremendous
momentum.
Similarly,
targeting
tumor
microenvironments
macrophages
an
area
exciting
we
have
only
scratch
surface
complicated
nature
oncology.
Cell
culture
studies
animal
models
provide
proof-of-concept
for
impetus
inhibition
Bufalin-related
clinical
are
insufficient
interdisciplinary
researchers
require
detailed
analysis
existing
gaps.
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(2), P. e24395 - e24395
Published: Jan. 1, 2024
BackgroundBufalin,
the
main
active
ingredient
of
traditional
Chinese
medicine
huachansu,
is
used
in
clinical
treatment
colorectal
cancer
and
has
multiple
effects,
including
inhibition
migratory
invasion,
reversal
multi-drug
resistance,
induction
apoptosis
differentiation,
angiogenesis.MethodsWe
collected
relevant
articles
on
bufalin
from
2003
to
2022
using
Web
Science
platform,
analysed
information
VOSviewer,
CiteSpace,
Microsoft
Excel
categorise
summarise
publications
over
past
20
years.ResultsWe
371
papers,
with
a
steady
increase
number
published
globally.
China
highest
articles,
whereas
Japan
citations.
Currently,
there
considerable
enthusiasm
for
investigating
anti-tumour
mechanism
optimising
drug
delivery
systems
its
administration.ConclusionFor
first
time,
we
present
comprehensive
overview
papers
worldwide
two
decades
progress
application
tumour
therapy.
We
summarised
key
authors,
institutions,
countries
that
have
contributed
field
potential
cancer.
This
will
help
other
researchers
obtain
an
field,
enhance
collaboration
knowledge
sharing,
promote
future
research
bufalin.
World Journal of Gastrointestinal Oncology,
Journal Year:
2025,
Volume and Issue:
17(4)
Published: March 24, 2025
The
study
conducted
by
Wang
et
al,
focuses
on
the
role
of
Rho
GTPase
activating
protein
12
(ARHGAP12),
in
hepatocellular
carcinoma
(HCC).
This
research
reveals
that
ARHGAP12
expression,
markedly
elevated
malignant
cells
HCC,
correlates
strongly
with
adverse
outcomes
for
patients.
Furthermore,
illustrates
enhances
ability
HCC
to
invade
and
contributes
their
resistance
tyrosine
kinase
inhibitors
(TKIs)
through
modulation
focal
adhesion
pathway.
To
comprehensively
investigate
relationship
between
TKI
resistance,
this
integrates
single-cell
bulk
RNA
sequencing
methodologies
along
data
from
tumor
immune
hub
2,
Gene
Expression
Omnibus,
Cancer
Genome
Atlas,
CellMiner,
Genomics
Drug
Sensitivity
as
well
immunohistochemical
staining
proteomic
analyses.
Statistical
analyses,
including
Wilcoxon
rank-sum
test
receiver
operating
characteristic
curve
analysis,
were
employed
evaluate
correlation
expression
levels
clinical
parameters,
drug
sensitivity.
It
is
evident
a
more
profound
exploration
molecular
dynamics
especially
those
related
against
TKIs,
essential.
International Journal of Nanomedicine,
Journal Year:
2024,
Volume and Issue:
Volume 19, P. 5581 - 5603
Published: June 1, 2024
Lenvatinib
(LVN)
is
a
potentially
effective
multiple-targeted
receptor
tyrosine
kinase
inhibitor
approved
for
treating
hepatocellular
carcinoma,
metastatic
renal
cell
carcinoma
and
thyroid
cancer.
Nonetheless,
poor
pharmacokinetic
properties
including
water
solubility
rapid
metabolic,
complex
tumor
microenvironment,
drug
resistance
have
impeded
its
satisfactory
therapeutic
efficacy.
This
article
comprehensively
reviews
the
uses
of
nanotechnology
in
LVN
to
improve
antitumor
effects.
With
characteristic
high
modifiability
loading
capacity
nano-drug
delivery
system,
an
active
targeting
approach,
controllable
release,
biomimetic
strategies
been
devised
deliver
target
tumors
sequence,
compensating
lack
passive
targeting.
The
existing
applications
advances
improving
efficacy
include
longer-term
efficiency,
achieving
higher
combination
therapy,
tracking
diagnosing
application
reducing
toxicity.
Therefore,
using
multiple
combined
with
photothermal,
photodynamic,
immunoregulatory
therapies
overcomes
multi-drug
resistance,
regulates
unfavorable
yields
synergistic
In
brief,
nano-LVN
system
has
brought
light
war
against
cancer
while
at
same
time
effect.
More
intelligent
multifunctional
nanoparticles
should
be
investigated
further
converted
into
clinical
future.
European Radiology Experimental,
Journal Year:
2024,
Volume and Issue:
8(1)
Published: March 12, 2024
Abstract
Background
Multi-
b
-value
diffusion-weighted
imaging
(DWI)
with
different
postprocessing
models
allows
for
evaluating
hepatocellular
carcinoma
(HCC)
proliferation,
spatial
heterogeneity,
and
feasibility
of
treatment
strategies.
We
assessed
synergistic
effects
bufalin+sorafenib
in
orthotopic
HCC-LM3
xenograft
nude
mice
by
using
intravoxel
incoherent
motion
(IVIM),
diffusion
kurtosis
(DKI),
a
stretched
exponential
model
(SEM),
fractional-order
calculus
(FROC)
model.
Methods
Twenty-four
were
divided
into
bufalin+sorafenib,
bufalin,
sorafenib
groups,
control
group.
DWI
was
performed
3-T
scanner
after
3
weeks’
to
obtain
true
coefficient
D
t
,
pseudo-diffusion
p
perfusion
fraction
f
mean
diffusivity
(MD),
(MK),
distributed
(DDC),
heterogeneity
index
α
D,
fractional
order
parameter
β
microstructural
quantity
μ
.
Necrotic
(NF),
standard
deviation
(SD)
hematoxylin-eosin
staining,
microvessel
density
(MVD)
anti-CD31
staining
evaluated.
Correlations
parameters
histopathological
results
analyzed,
measurements
compared
among
four
groups.
Results
In
the
final
22
mice,
positively
correlated
MVD
(
r
=
0.679,
0.001).
Significantly
good
correlations
MK
0.677),
-0.696),
-0.639)
SD
observed
(all
<
0.010).
MK,
MVD,
much
lower,
while
MD,
NF
higher
bufalin
plus
group
than
0.050).
Conclusion
Evaluated
IVIM,
DKI,
SEM,
FROC,
found
inhibit
tumor
proliferation
angiogenesis
reduce
models.
Relevance
statement
b-
value
provides
potential
metrics
efficacy
HCC.
Key
points
•
Bufalin
combination
may
increase
effectiveness
HCC
therapy.
depicted
angiogenesis,
heterogeneity.
be
noninvasive
method
assess
therapeutic
efficacy.
Graphical