Jundishapur Journal of Natural Pharmaceutical Products,
Journal Year:
2024,
Volume and Issue:
19(4)
Published: Dec. 1, 2024
Background:
Shikonin,
a
compound
extracted
from
Lithospermum
erythrorhizon,
has
demonstrated
therapeutic
effects
on
cancer;
however,
its
oral
cancer
remain
unclear.
Objectives:
This
study
aimed
to
explore
the
value
of
shikonin
for
treatment
cancer.
Methods:
MTT,
colony
formation,
and
Transwell
assays
were
employed
evaluate
inhibitory
proliferation
migration
abilities
human
cell
lines
(SCC-4
SAS).
Apoptosis
viability
assessed
using
TdT-mediated
deoxyuridine
triphosphate-biotin
nick
end-labeling
(TUNEL)
assay.
To
investigate
potential
anticancer
mechanisms
shikonin,
RNA
sequencing,
quantitative
PCR,
western
blotting
performed
analyze
changes
in
expression
levels
cell-related
genes
proteins
(matrix
metalloproteinases-2
(MMP-2),
matrix
metalloproteinases-9
(MMP-9),
VEGF-A,
VEGF-C,
Beclin-1,
autophagy-related
(ATG5),
light
chain-3
(LC-3)).
Additionally,
animal
xenograft
experiments
conducted
examine
vivo
antitumor
shikonin.
Results:
The
findings
revealed
that
external
application
specifically
targeted
cells
without
affecting
normal
led
dose-dependent
inhibition
their
growth.
Even
at
non-lethal
doses,
effectively
suppressed
production
metalloproteinases,
thereby
inhibiting
wound
healing.
Furthermore,
reduced
tumor
progression
factors,
such
as
vascular
endothelial
growth
factor
(VEGF)-A
which
are
released
during
early
stages
angiogenesis
lymphangiogenesis.
Meanwhile,
higher
doses
induced
autophagy
activated
ATG-5,
LC-3B,
Beclin-1.
At
lethal
further
decreased
mitochondrial
membrane
potential,
calcium
ions,
triggered
apoptotic
pathways.
However,
administration
ion
chelator
(BAPTA-AM)
inhibited
shikonin-induced
apoptosis.
Conclusions:
These
results
demonstrate
induces
activates
pathways
cells.
Shikonin
significantly
apoptosis
rat
model.
In
conclusion,
growth,
metastasis,
progression-related
proteins.
Given
ease
drug
delivery
affected
area
cancer,
holds
substantial
future
applications
may
improve
patient
recovery
enhance
cure
rates.
European Journal of Medicinal Chemistry,
Journal Year:
2024,
Volume and Issue:
268, P. 116249 - 116249
Published: Feb. 23, 2024
Cancer
encompasses
a
group
of
pathologies
with
common
characteristics,
high
incidence,
and
prevalence
in
all
countries.
Although
there
are
treatments
available
for
this
disease,
they
not
always
effective
or
safe,
often
failing
to
achieve
the
desired
results.
This
is
why
it
necessary
continue
search
new
therapies.
One
strategies
obtaining
antitumor
drugs
use
1,4-naphthoquinone
as
scaffold
synthetic
natural
products
activity.
review
focuses
on
compiling
studies
related
activity
its
derivatives
over
last
10
years.
The
work
describes
main
naphthoquinones
classifies
based
structural
modifications
made
scaffold.
Additionally,
formation
metal
complexes
using
ligand
considered.
After
thorough
review,
197
compounds
potent
biological
against
cancer
have
been
classified
according
their
chemical
structures
mechanisms
action
described.
Acta Pharmaceutica Sinica B,
Journal Year:
2024,
Volume and Issue:
14(7), P. 2815 - 2853
Published: April 24, 2024
Regulated
cell
death
(RCD)
is
a
controlled
form
of
orchestrated
by
one
or
more
cascading
signaling
pathways,
making
it
amenable
to
pharmacological
intervention.
RCD
subroutines
can
be
categorized
as
apoptotic
non-apoptotic
and
play
essential
roles
in
maintaining
homeostasis,
facilitating
development,
modulating
immunity.
Accumulating
evidence
has
recently
revealed
that
evasion
frequently
the
primary
cause
tumor
survival.
Several
have
garnered
attention
promising
cancer
therapies
due
their
ability
induce
regression
prevent
relapse,
comparable
apoptosis.
Moreover,
they
offer
potential
solutions
for
overcoming
acquired
resistance
tumors
toward
drugs.
With
an
increasing
understanding
underlying
mechanisms
governing
these
subroutines,
growing
number
small-molecule
compounds
targeting
single
multiple
pathways
been
discovered,
providing
novel
strategies
current
therapy.
In
this
review,
we
comprehensively
summarized
regulatory
emerging
mainly
including
autophagy-dependent
death,
ferroptosis,
cuproptosis,
disulfidptosis,
necroptosis,
pyroptosis,
alkaliptosis,
oxeiptosis,
parthanatos,
mitochondrial
permeability
transition
(MPT)-driven
necrosis,
entotic
NETotic
lysosome-dependent
immunogenic
(ICD).
Furthermore,
focused
on
discussing
related
compounds.
brief,
insightful
findings
may
provide
valuable
guidance
investigating
individual
collaborative
approaches
towards
different
ultimately
driving
discovery
target
significantly
enhance
future
therapeutics.
International Journal of Nanomedicine,
Journal Year:
2024,
Volume and Issue:
Volume 19, P. 2507 - 2528
Published: March 1, 2024
Background:
Cancer
continues
to
be
a
prominent
issue
in
the
field
of
medicine,
as
demonstrated
by
recent
studies
emphasizing
significant
role
autophagy
development
cancer.
Traditional
Chinese
Medicine
(TCM)
provides
variety
anti-tumor
agents
capable
regulating
autophagy.
However,
clinical
application
autophagy-modulating
compounds
derived
from
TCM
is
impeded
their
restricted
water
solubility
and
bioavailability.
To
overcome
this
challenge,
utilization
nanotechnology
has
been
suggested
potential
solution.
Nonetheless,
current
body
literature
on
nanoparticles
delivering
TCM-derived
for
cancer
treatment
limited,
lacking
comprehensive
summaries
detailed
descriptions.
Methods:
Up
November
2023,
research
study
was
conducted
gather
relevant
data
using
databases,
including
PubMed,
ScienceDirect,
Springer
Link,
Web
Science,
CNKI.
The
keywords
utilized
investigation
included
"autophagy",
"nanoparticles",
"traditional
medicine"
"anticancer".
Results:
This
review
analysis
overcoming
delivery
challenges
enhancing
anti-cancer
properties
TCM.
evaluation
based
synthesis
different
classes
TCM,
mechanisms
action
treatment,
benefits
reported
various
scholarly
sources.
findings
indicate
that
shows
availability
thereby
opening
up
plethora
therapeutic
avenues.
Conclusion:
Nanotechnology
enhance
efficacy
traditional
through
regulation
Keywords:
autophagy,
nano-delivery,
anti-cancer,
medicine
Phytotherapy Research,
Journal Year:
2024,
Volume and Issue:
38(9), P. 4353 - 4385
Published: July 3, 2024
Autophagy
and
endoplasmic
reticulum
(ER)
stress
are
conserved
processes
that
generally
promote
survival,
but
can
induce
cell
death
when
physiological
thresholds
crossed.
The
pro-survival
aspects
of
these
exploited
by
cancer
cells
for
tumor
development
progression.
Therefore,
anticancer
drugs
targeting
autophagy
or
ER
to
and/or
block
the
being
investigated
extensively.
Consistently,
several
phytochemicals
have
been
reported
exert
their
effects
modulating
stress.
Various
(e.g.,
celastrol,
curcumin,
emodin,
resveratrol,
among
others)
activate
unfolded
protein
response
stress-mediated
apoptosis
through
different
pathways.
Similarly,
various
mechanisms
(namely
mechanistic
target
Rapamycin
[mTOR]
inhibition).
However,
phytochemical-induced
function
either
as
a
cytoprotective
mechanism
programmed
type
II.
Interestingly,
at
times,
same
phytochemical
6-gingerol,
shikonin,
II
depending
on
cellular
contexts,
such
type.
Although
there
is
well-documented
interplay
between
stress,
only
one-way
modulation
was
noted
with
some
(carnosol,
capsaicin,
cryptotanshinone,
guangsangon
E,
kaempferol,
δ-tocotrienol):
stress-dependent
autophagy.
Plant
extracts
sources
potent
while
numerous
in
preclinical
clinical
studies,
search
novel
ongoing
from
plant
used
traditional
medicine
Origanum
majorana).
Nonetheless,
translation
phytochemicals,
promising
avenue
therapeutics,
hindered
limitations
need
be
addressed
future
studies.
Journal of Chemical Research,
Journal Year:
2025,
Volume and Issue:
49(1)
Published: Jan. 1, 2025
A
total
synthesis
of
the
natural
polycyclic
phenolic
compound
daldiquinone
was
reported
derived
from
1-naphthaldehyde.
The
utilizes
regioselective
peri-C-H
oxidation
as
a
key
step,
proceeding
through
longest
linear
sequence
seven
steps
with
an
overall
yield
40%.
binaphthol
intermediate
is
obtained
via
Baeyer-Villiger
oxidative
rearrangement
in
81%
yield,
followed
by
IBX
to
produce
naphthoquinone.
binaphthalene
core
constructed
using
Suzuki
coupling.
This
strategy,
which
relied
on
direct
C-H
bond
naphthalene
ring,
significantly
truncated
synthetic
pathway
and
boosted
efficiency.
regiospecific
approach
offers
promising
for
obtaining
wide
array
derivatives.