Lung
cancer
is
one
of
the
cancers
with
highest
mortality
rates.
Non-small
cell
lung
(NSCLC)
accounts
for
85%
cases
and
often
diagnosed
at
an
advanced
stage
a
poor
prognosis.
Due
to
lack
effective
molecular
targets,
current
clinical
cure
rate
low,
recurrence
high.
Recent
studies
have
found
that
active
components
traditional
Chinese
medicine
herbal
formulas
can
inhibit
development
NSCLC
through
multiple
pathways
effectively
reducing
its
metastasis
rates,
improving
treatment
side
effects,
compensating
deficiencies
in
drug
resistance.
Although
treatments
such
as
surgery,
radiotherapy,
targeted
therapy,
immunotherapy
achieved
better
efficacy
treating
cancer,
they
still
problems
complications
severe
adverse
reactions.
In
recent
years,
numerous
basic
confirmed
good
effects
cancer.
Traditional
has
synergistic
regulatory
effect
components,
pathways,
channels.
The
monomeric
complex
mechanisms
action
determine
there
are
issues
unclear
related
prevention
by
medicine.
There
urgent
need
elucidate
intervening
from
perspective
modern
medicine,
levels
biology,
network
pharmacology,
etc.
This
article
systematically
summarizes
research
progress
on
regulation
above-mentioned
signaling
expression
key
protein
molecules
monomers
or
formulas,
aiming
clarify
progression
provide
ideas
theoretical
basis
in-depth
study
application
Journal of Cancer,
Journal Year:
2024,
Volume and Issue:
15(7), P. 2024 - 2032
Published: Jan. 1, 2024
Objective:
This
study
evaluated
the
efficacy
and
safety
of
gemcitabine
oxaliplatin
intrathoracic
perfusion
chemotherapy
(IPCGOR)
regimen
combined
with
interleukin-2
(IL-2)
for
advanced
non-small
cell
lung
cancer
(NSCLC).Methods:
We
conducted
a
retrospective
analysis
460
NSCLC
patients
from
Yunnan
Province
Early
Cancer
Diagnosis
Treatment
Project
(June
2020-October
2022),
assessing
IPCGOR
IL-2
combination.Outcomes
were
measured
based
on
RECIST
1.1
criteria,
focusing
objective
response
rate
(ORR),
disease
control
(DCR),
median
progression-free
survival
(mPFS),
overall
(MOS),
treatment
safety.Results:
The
demonstrated
an
ORR
67.4%,
DCR
97.4%,
mPFS
8.5
months,
MOS
12.5
months.14
underwent
successful
surgery
post-treatment.Common
adverse
reactions
manageable,
no
treatment-related
deaths
reported.
Conclusion:The
shows
promising
tolerable
profile
NSCLC.These
findings
suggest
its
potential
as
reference
treating
NSCLC.However,
study's
nature
single-center
design
pose
limitations.Future
research
should
focus
prospective
studies,
randomized
controlled
trials,
long-term
outcome
assessments,
particularly
in
diverse
patient
subgroups,
to
further
validate
refine
clinical
application
this
regimen.
Journal of Clinical Medicine,
Journal Year:
2024,
Volume and Issue:
13(7), P. 2046 - 2046
Published: April 1, 2024
Over
the
past
two
decades,
prognosis
in
adolescents
and
young
adults
(AYAs)
diagnosed
with
acute
myeloid
leukemia
(AML)
has
significantly
improved.
The
standard
intensive
cytotoxic
treatment
approach
for
AYAs
AML,
consisting
of
induction
chemotherapy
anthracycline/cytarabine
combination
followed
by
consolidation
or
stem
cell
transplantation,
lately
been
shifting
toward
novel
targeted
therapies,
mostly
fields
clinical
trials.
One
most
recent
advances
treating
AML
is
B-cell
lymphoma
2
(Bcl-2)
inhibitor
venetoclax
hypomethylating
agents,
which
studied
elderly
populations
was
approved
Food
Drug
Administration
(FDA)
patients
over
75
years
age
excluded
from
schemas
due
to
comorbidities.
Regarding
AYA
population,
therapy
could
be
a
therapeutic
option
refractory/relapsed
(R/R)
although
data
real-world
studies
are
currently
limited.
Venetoclax
frequently
used
advanced
hematologic
malignancies,
mainly
lymphoblastic
myelodysplastic
syndromes,
as
salvage
considerable
efficacy
safety.
Herein,
we
aim
summarize
evidence
obtained
trials
observational
on
use
AML.
Based
available
evidence,
safe
effective
R/R
patients.
However,
further
research
larger
cohorts
needed
confirm
these
data,
establishing
benefits
venetoclax-based
regimen
this
special
population.
Frontiers in Neuroscience,
Journal Year:
2025,
Volume and Issue:
18
Published: Jan. 15, 2025
Intracerebral
hemorrhage
(ICH)
is
a
major
public
health
challenge
worldwide,
and
associated
with
elevated
rates
of
mortality,
disability,
morbidity,
especially
in
low-
middle-income
nations.
However,
our
knowledge
the
detailed
molecular
processes
involved
ICH
remains
insufficient,
particularly
those
secondary
injury
stage,
resulting
lack
effective
treatments
for
ICH.
Human
platelet
lysates
(HPL)
are
abundant
bioactive
factors,
numerous
studies
have
demonstrated
their
beneficial
effects
on
neurological
diseases,
including
anti-neuroinflammatory
ability,
anti-oxidant
effects,
maintenance
blood-brain
barrier
integrity,
promotion
neurogenesis.
In
this
review,
we
thoroughly
explore
potential
HPL
treating
from
three
critical
perspectives:
rationale
selecting
as
treatment
ICH,
mechanisms
through
which
contributes
to
management,
additional
measures
necessary
We
elucidate
role
platelets
pathophysiology
highlight
limitations
current
options
advancements
preclinical
research
application
disorders.
Furthermore,
historical
developments
preparation
methods
field
biomedicine
discussed.
Additionally,
summarize
molecules
present
therapeutic
Finally,
outline
issues
that
must
be
addressed
regarding
utilizing
modality
Objective:
This
study
investigates
the
development
trends
and
research
hotspots
in
clinical
testing
for
multiple
myeloma
from
2000
to
2023,
using
bibliometric
techniques.
Method:
Search
relevant
literature
on
of
published
Web
Science
Core
Collection
(WoSCC)
use
CiteSpace
6.2.R4
software
draw
a
visual
knowledge
map
authors,
institutions,
national
regional
cooperation
networks,
journals,
keywords,
conduct
analysis.
Results:
The
found
an
upward
trend
publications
over
specified
period,
with
significant
growth
noted
2012
onwards.
majority
originates
United
States,
contributions
institutions
like
Mayo
Clinic
MD
Anderson
Cancer
Center.
Analysis
author
collaboration
networks
indicated
relatively
low
centrality,
suggesting
minimal
among
researchers.
Bibliometric
mapping
highlighted
several
field
including
therapeutic
strategies
involving
proteasome
inhibitors
immunomodulatory
drugs,
role
stem
cell
transplantation,
importance
achieving
monitoring
residual
disease.
Conclusion:
is
characterized
by
growing
body
research,
States.
Despite
increasing
volume
there
need
enhanced
researchers
consolidate
findings
advance
practice.
Frontiers in Oncology,
Journal Year:
2025,
Volume and Issue:
14
Published: Jan. 21, 2025
Apoptosis
is
an
essential
characteristic
of
cancer
and
its
dysregular
promotes
tumor
growth,
clonal
evolution,
treatment
resistance.
B-cell
lymphoma-2
(BCL-2)
protein
family
members
are
key
to
the
intrinsic,
mitochondrial
apoptotic
pathway.
The
inhibition
BCL-2
pro-survival
proteins,
which
frequently
overexpressed
in
malignancies
pose
a
fundamental
carcinogenic
mechanism
has
been
proposed
as
promising
therapeutic
option,
with
venetoclax
(ABT-199)
being
first
FDA-approved
inhibitor.
Unfortunately,
although
shown
remarkable
results
range
lymphoid
cancers
well
acute
myeloid
leukemia
(AML),
development
resistance
significantly
reduces
response
rates
specific
subtypes.
In
this
article,
we
explain
role
proteins
apoptosis
their
action
that
justifies
potential
target
malignancies,
including
chronic
lymphocytic
leukemia,
multiple
myeloma,
lymphomas,
but
also
AML.
We
further
analyze
characteristics
result
intrinsic
or
inherited
inhibitors.
Finally,
focus
on
biomarkers
can
be
used
predict
responses
name
personalized
medicine,
goal
exploring
alternative
strategies
overcome
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.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(17), P. 9143 - 9143
Published: Aug. 23, 2024
Besides
producing
cellular
energy,
mitochondria
are
crucial
in
controlling
oxidative
stress
and
modulating
metabolism,
particularly
under
stressful
conditions.
A
key
aspect
of
this
regulatory
role
involves
the
recycling
process
autophagy,
which
helps
to
sustain
energy
homeostasis.
Autophagy,
a
lysosome-dependent
degradation
pathway,
plays
fundamental
maintaining
homeostasis
by
degrading
damaged
organelles
misfolded
proteins.
In
context
tumor
formation,
autophagy
significantly
influences
cancer
metabolism
chemotherapy
resistance,
contributing
both
suppression
surveillance.
This
review
focuses
on
relationship
between
specifically
progression.
Investigating
interaction
reveals
new
possibilities
for
treatments
may
result
development
more
effective
therapies
targeting
mitochondria,
could
have
significant
implications
treatment.
Additionally,
highlights
increasing
understanding
autophagy’s
development,
with
focus
mitochondrial
function
pre-clinical
clinical
research.
It
also
explores
potential
developing
more-targeted
personalized
investigating
autophagy-related
biomarkers.