Knowledge map of programmed cell death in esophageal cancer: a bibliometric analysis
Rulin Li,
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Yanchun Yang,
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Yang Gao
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et al.
Discover Oncology,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: April 24, 2025
This
study
aimed
to
delineate
the
evolving
knowledge
structure
of
programmed
cell
death
in
esophageal
cancer
and
identify
key
thematic
trends,
influential
collaborations,
emerging
areas
for
future
research.
A
bibliometric
approach
was
applied
2677
publications
retrieved
from
Web
Science
Core
Collection
(2000-2024).
Three
complementary
tools-CiteSpace,
VOSviewer,
bibliometrix-were
employed
visualize
co-citation
networks,
detect
citation
bursts,
map
collaborative
patterns
among
authors,
institutions,
countries.
Inclusion
criteria
focused
on
articles
reviews
that
addressed
conjunction
with
apoptosis,
necroptosis,
pyroptosis,
ferroptosis,
autophagy,
or
related
pathways.
Publication
outputs
grew
markedly,
reflecting
a
shift
early
investigations
basic
apoptotic
mechanisms
broader
explorations
ferroptosis.
China
led
publication
volume
citations,
driven
by
substantial
governmental
funding
large
clinical
cohorts.
The
United
States
Japan
also
contributed
significantly,
forming
international
research
networks
spanned
Asia
Europe.
Leading
particularly
Zhengzhou
University,
demonstrated
extensive
collaborations.
Journals
such
as
Oncology
Letters
Reports
were
prominent
outlets
new
findings,
while
highly
cited
references
highlighted
hypoxia,
immune
checkpoint
blockade,
gene-editing
strategies.
Keyword
analyses
revealed
ascendance
immuno-oncology,
network
pharmacology,
translational
applications
targeting
multiple
regulated
Bibliometric
evidence
underscores
rapid
expansion
multidisciplinary
integrates
diverse
pathways
cancer.
Continued
leveraging
advanced
genomics
immunologic
strategies,
are
poised
accelerate
breakthroughs
enable
more
personalized,
effective
therapies.
Language: Английский
Biogenic synthesized CuO nanoparticles and 5-fluorouracil loaded anticancer gel for HeLa cervical cancer cells
Discover Nano,
Journal Year:
2024,
Volume and Issue:
19(1)
Published: Dec. 27, 2024
Abstract
Cervical
cancer
remains
a
significant
health
challenge
in
developing
countries
are
high
due
to
low
HPV
vaccination
rates,
delayed
diagnosis,
and
restricted
healthcare
access.
Metal
nanomaterials,
such
as
copper
oxide
(CuO)
nanoparticles
(NPs),
have
shown
promise
therapy
their
ability
induce
apoptosis.
5-Fluorouracil
(5-Fu)
enhances
the
cytotoxic
effect
against
cervical
cancer,
working
synergistically
with
CuO
NPs
maximize
therapeutic
impact
while
potentially
reducing
5-Fu's
systemic
side
effects.
This
study
explores
synergistic
potential
of
green-synthesized
combined
5-Fu
gel
formulation
for
targeted
anticancer
activity
HeLa
cells.
were
synthesized
using
Trichosanthes
dioica
dried
seeds
extract
incorporated
into
pectin-xanthan
gum-based
gel.
The
exhibited
zeta
−23.7
mV,
particle
size
approximately
26
nm,
spherical
morphology.
Characterization
studies,
including
FTIR,
viscosity,
spreadability,
pH,
stability
assessments,
confirmed
gel's
suitability
vaginal
delivery.
In-vitro
drug
release
showed
xanthan
gum
extended
up
8
h.
MTT
assay
revealed
PXFCu6
IC
50
at
11.82
±
0.22
μg/mL,
significantly
more
cells,
being
3.62
times
potent
than
(IC
:
42.8
0.24
μg/mL)
1.63
alone
19.3
0.49
μg/mL).
antibacterial
no
inhibition
plain
gel,
but
T.
-mediated
22.35
4.9
mm.
had
52.05
1.37
mm
Escherichia
coli
growth.
better
4
°C,
maintaining
release,
unlike
25
°C
where
mild
degradation
occurred.
research
highlights
NPs-5-Fu
novel,
effective
strategy
treatment.
Graphical
abstract
Language: Английский