Forests,
Journal Year:
2023,
Volume and Issue:
14(6), P. 1172 - 1172
Published: June 6, 2023
(1)
Anthracnose
caused
by
Colletotrichum
damages
crops,
ornamentals,
and
forest
trees
severely,
resulting
in
enormous
economic
losses
to
agricultural
forestry
systems.
Overusing
traditional
chemical
fungicides
leads
fungicide
resistance,
environmental
pollution,
potential
risks
public
health.
Therefore,
priorities
should
be
given
developing
efficient
environmentally
friendly
approaches
phytopathogens
management,
including
anthracnose.
(2)
In
this
study,
the
antifungal
activity
of
botanical
derivative
polysubstituted
cyclic
1,2-diketones
(FPL001)
against
C.
gloeosporioides
was
examined.
(3)
FPL001
significantly
inhibited
vegetative
growth
with
an
EC50
160.23
µg/mL.
When
concentration
reached
30
µg/mL,
conidial
germination
appressorium
formation
were
completely
inhibited.
also
suppressed
invasive
hyphae
development
plant
infection
gloeosporioides.
did
not
exhibit
toxicity
model
organisms
such
as
alfalfa
silkworm
larvae.
(4)
These
results
indicate
that
compound
is
a
agent
for
green
control
Biologics,
Journal Year:
2024,
Volume and Issue:
Volume 18, P. 229 - 255
Published: Sept. 1, 2024
Natural
products
have
proven
to
be
promising
anti-cancer
agents
due
their
diverse
chemical
structures
and
bioactivity.This
review
examines
central
role
in
cancer
treatment,
focusing
on
mechanisms
of
action
therapeutic
benefits.Medicinal
plants
contain
bioactive
compounds,
such
as
flavonoids,
alkaloids,
terpenoids
polyphenols,
which
exhibit
various
anticancer
properties.These
compounds
induce
apoptosis,
inhibit
cell
proliferation
cycle
progression,
interfere
with
microtubule
formation,
act
topoisomerase
targets,
angiogenesis,
modulate
key
signaling
pathways,
improve
the
tumor
microenvironment,
reverse
drug
resistance
activate
immune
cells.Herbal
drugs
offer
advantages,
particularly
selective
toxicity
against
cells,
reducing
adverse
side
effects
associated
conventional
chemotherapy.Recent
studies
clinical
trials
highlight
benefits
herbal
medicines
alleviating
effects,
improving
tolerance
chemotherapy
occurrence
synergistic
treatments.For
example,
medicine
SH003
was
found
safe
potentially
effective
treatment
solid
cancers,
while
Fucoidan
showed
anti-inflammatory
properties
that
are
beneficial
for
patients
advanced
cancer.The
current
research
landscape
is
extensive.Numerous
investigating
efficacy,
safety
cancers
lung,
prostate,
breast
hepatocellular
carcinoma.Promising
developments
include
polypharmacological
approach,
combination
therapies,
immunomodulation
improvement
quality
life.However,
there
still
challenges
development
use
natural
drugs,
need
further
into
action,
possible
interactions
optimal
dosage.Standardizing
extracts,
bioavailability
delivery,
overcoming
regulatory
acceptance
hurdles
critical
issues
addressed.Nonetheless,
warrant
investigation
development.Multidisciplinary
collaboration
essential
advance
therapy
integrate
these
mainstream
treatment.
Pharmaceuticals,
Journal Year:
2024,
Volume and Issue:
17(5), P. 598 - 598
Published: May 8, 2024
In
the
current
work,
synergy
between
natural
compounds
and
conventional
chemotherapeutic
drugs
is
comprehensively
reviewed
in
light
of
preclinical
research
findings.
The
prognosis
for
lung
cancer
patients
poor,
with
a
5-year
survival
rate
18.1%.
use
combination
has
gained
significant
attention
as
potential
novel
approach
treatment
cancer.
present
work
highlights
importance
finding
more
effective
therapies
to
increase
rates.
Chemotherapy
primary
option
but
it
limitations
such
reduced
effectiveness
because
cells
become
resistant.
Natural
isolated
from
medicinal
plants
have
shown
promising
anticancer
or
chemopreventive
properties
their
synergistic
effect
been
observed
when
combined
therapies.
an
anti-cancer
drug
compound
exhibits
effects,
enhancing
overall
therapeutic
actions
against
cells.
conclusion,
this
provides
overview
latest
on
plant-derived
alternative
complementary
options
chemotherapy
discusses
treating
minimal
side
effects.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 29, 2025
Abstract
Methods
The
ethanolic
roots
(CCRE)
and
leaves
(CCLE)
extracts
were
interrogated
for
their
apoptotic
potential
against
human
lung
adenocarcinoma
cell
line
(A549)
using
DNA
fragmentation,
Annexin
V-FITC/PI
staining
apoptosis
assay
cycle
analysis
flow
cytometry.
Results
Our
results
revealed
significant
damage
induced
death
in
A549
on
treatment
with
active
concentrations
(40
µg/ml
80
µg/ml)
of
the
S
phase
arrest.
Conclusions
This
is
first
study
demonstrating
inducing
chemically
characterized
bioactive
compounds
present
from
Chlorophytum
comosum
non-small
line.
concludes
that
can
be
a
candidate
natural
isolated,
clinically
evaluated
development
novel
naturally
derived
anti-cancer
drugs
cancer.
Pharmaceuticals,
Journal Year:
2025,
Volume and Issue:
18(5), P. 644 - 644
Published: April 28, 2025
Despite
numerous
advances
in
treatment,
cancer
still
remains
a
leading
cause
of
death
worldwide.
Given
the
significant
health
and
economic
burden
this
disease
imposes,
it
is
important
to
explore
more
effective
treatment
strategies.
A
major
drawback
conventional
therapies
persistence
drug
resistance,
adverse
reactions
chemotherapy,
digestive
damage,
reduced
quality
life,
high
costs.
To
address
these
challenges,
researchers
have
been
investigating
utility
using
complementary
alternative
medicine
(CAM)
alongside
treatments.
Some
CAM
approaches
reported
enhance
patients’
life
reduce
severity
effects
from
therapies.
This
review
explores
traditional
Chinese,
Korean,
Indian,
Japanese,
South
African
medicines
as
supportive
for
We
also
discuss
concept
integrative
oncology
its
global
relevance,
typically
emphasize
whole-person
care,
including
diet,
lifestyle,
mental/emotional
well-being.
In
addition,
we
identify
key
active
phytochemicals
herbal
used
systems
treatment.
Our
discussion
aims
provide
foundation
future
research
into
oncology,
fostering
an
interdisciplinary
approach
management.
Phytotherapy Research,
Journal Year:
2024,
Volume and Issue:
38(8), P. 3899 - 3920
Published: May 28, 2024
Abstract
Lung
cancer,
the
second
leading
cause
of
cancer‐related
deaths,
accounts
for
a
substantial
portion,
representing
18.4%
all
cancer
fatalities.
Despite
advances
in
treatment
modalities
such
as
chemotherapy,
surgery,
and
immunotherapy,
significant
challenges
persist,
including
chemoresistance,
non‐specific
targeting,
adverse
effects.
Consequently,
there
is
an
urgent
need
innovative
therapeutic
approaches
to
overcome
these
limitations.
Natural
compounds,
particularly
phytoconstituents,
have
emerged
promising
candidates
due
their
potent
anticancer
properties
relatively
low
incidence
effects
compared
conventional
treatments.
However,
inherent
poor
solubility,
rapid
metabolism,
enzymatic
degradation
hinder
clinical
utility.
To
address
obstacles,
researchers
increasingly
turned
nanotechnology‐based
drug
delivery
systems
(DDS).
Nanocarriers
offer
several
advantages,
enhanced
stability,
prolonged
circulation
time,
targeted
tumor
sites,
thereby
minimizing
off‐target
By
encapsulating
phytoconstituents
within
nanocarriers,
aim
optimize
bioavailability
efficacy
while
reducing
systemic
toxicity.
Moreover,
integration
nanotechnology
with
allows
nuanced
understanding
intricate
molecular
pathways
involved
lung
pathogenesis.
This
integrated
approach
holds
promise
modulating
key
cellular
processes
implicated
growth
progression.
Additionally,
by
leveraging
synergistic
seek
develop
tailored
strategies
that
maximize
In
conclusion,
nanocarriers
represents
avenue
advancing
treatment.
has
potential
revolutionize
current
paradigms
offering
targeted,
efficient,
minimally
toxic
interventions.
Continued
research
this
field
improving
patient
outcomes
addressing
unmet
needs
management.
Pharmacognosy Magazine,
Journal Year:
2024,
Volume and Issue:
20(4), P. 1276 - 1285
Published: Aug. 16, 2024
Background
The
predisposition
toward
gastrointestinal
disease
is
increasing
as
a
result
of
dietary
changes
and
overindulgence
in
food
preparation.
Ninety
percent
stomach
cancers
are
adenocarcinomas,
type
cancer
the
tract
that
leading
cause
mortality
worldwide.
Purpose
Astilbin,
natural
dihydroflavonol
substance
derived
from
range
foods
medicinal
herbs,
has
been
shown
current
study
to
have
anticancer
potential
against
gastric
AGS
cell
lines.
Materials
Methods
half
maximal
inhibitory
concentration
value
was
determined
after
astilbin
given
lines
at
various
doses.
To
verify
apoptosis,
astilbin-treated
line
subsequently
stained
with
dual
dye
acridine
orange/ethidium
bromide.
lines,
enzyme-linked
immunosorbent
assay
(ELISA)
approach
also
used
investigate
inflammatory
cytokines.
Using
ELISA,
apoptotic
marker
expression
including
Bcl-2-associated
X-protein,
caspase-9
proteins,
B-cell
lymphoma
2
assessed
cells
treated
astilbin.
Results
study’s
findings
reveal
prime
candidate
for
therapy
since
it
causes
apoptosis
stronger
effect
on
major
markers
disease.
Conclusion
provides
comprehensive
methodologies
tools
predicting
absorption,
distribution,
metabolism,
excretion,
toxicity
properties,
facilitating
informed
decision-making
development
optimization
therapy.
BMC Complementary Medicine and Therapies,
Journal Year:
2024,
Volume and Issue:
24(1)
Published: July 15, 2024
Medicinal
plant-mediated
combinational
therapies
have
gained
importance
globally
due
to
minimal
side
effects
and
enhanced
treatment
outcomes
compared
single-drug
modalities.
We
aimed
analyze
the
cytotoxic
potential
of
each
conventional
i.e.,
photodynamic
therapy
(PDT),
chemotherapy
(doxorubicin
hydrochloride;
Dox-HCl)
with
or
without
various
concentrations
medicinal
plant
extracts
(PE)
on
soft
tissue
cancer
Rhabdomyosarcoma
(RD)
cell
line.
Journal of Toxicology and Environmental Health,
Journal Year:
2023,
Volume and Issue:
87(2), P. 57 - 76
Published: Nov. 6, 2023
The
present
study
aimed
to
determine
the
biological
properties
of
an
extract
Solanum
aculeatissimum
aqueous
(SaCE)
alone
as
well
silver
nanoparticles
(AgNPs)
generated
by
green
synthesis
utilizing
S.
(SaCE).
These
synthesized
SaCE
AgNPs
were
characterized
using
UV-VIS
spectrophotometry,
scanning
transmission
electron
microscopy
(TEM),
energy
dispersive
spectroscopy
(EDS),
zeta
potential
(ZP),
dynamic
light
scattering
(DLS).
Determination
total
polyphenols,
flavonoids,
saponins
content
was
conducted.
In
addition,
high
performance
liquid
chromatography-mass
spectrometry
(HPLC-MS)
employed
identify
constituents
in
this
extract.
Antioxidant
activity
determined
DPPH
radical
scavenging
and
ferric
ion
reducing
power
(FRAP)
methods.
Antiglycation
demonstrated
through
relative
mobility
electrophoresis
(RME)
determination
free
amino
groups.
inhibitory
on
tyrosinase
also
examined.
Molecular
docking
analyses
performed
assess
molecular
interactions
with
DNA
tyrosinase.
antitumor
measured.
Phytochemical
analysis
showed
presence
polyphenols
(1000.41
293.37
mg
gallic
acid
equivalent/g),
flavonoids
(954.87
479.87
rutin
(37.89
23.01%
saponins),
particular
steroidal
(aculeatiside
A
B).
Both
exhibited
significant
antioxidant
(respectively,
73.97%,
56.27%
test,
874.67
837.67
μM
Trolox
Equivalent/g
FRAP
test)
antiglycation
activities
(72.81
67.98%
groups,
results
observed
RME).
presented
33.2,
36.1%
tyrosinase,
respectively.
silico
assay
interaction
between
saponins,
or
action
against
various
human
tumor
cells.
Data
that
extracts
from
interest
for
application
new
therapeutic
formulations
medicine.