Vaccines,
Год журнала:
2023,
Номер
12(1), С. 45 - 45
Опубликована: Дек. 30, 2023
The
incidence
of
thyroid
cancer
(TC)
has
increased
over
the
past
30
years.
Although
differentiated
(DTC)
a
good
prognosis
in
most
patients
undergoing
total
thyroidectomy
followed
by
radioiodine
therapy
(RAI),
5–10%
develop
metastasis.
Anaplastic
(ATC)
low
survival
rate
and
few
effective
treatments
have
been
available
to
date.
Recently,
tyrosine
kinase
inhibitors
(TKIs)
successfully
applied
RAI-resistant
or
non-responsive
TC
suppress
disease.
However,
eventually
develops
resistance
TKIs.
Immunotherapy
is
promising
treatment
for
TC,
majority
which
considered
an
immune-hot
malignancy.
Immune
suppression
cells
immune-suppressing
cells,
including
tumor-associated
macrophages,
myeloid-derived
suppressor
regulatory
T
complex
dynamic.
Negative
immune
checkpoints,
cytokines,
vascular
endothelial
growth
factors
(VEGF),
indoleamine
2,3-dioxygenase
1
(IDO1)
antitumor
cells.
Basic
translational
advances
checkpoint
(ICIs),
molecule-targeted
therapy,
tumor-specific
immunotherapy,
their
combinations
enabled
us
overcome
activate
This
review
summarizes
current
findings
regarding
microenvironment,
immunosuppression,
immunological
targets,
immunotherapy
highlights
potential
efficacy
immunotherapy.
Cancer Communications,
Год журнала:
2023,
Номер
44(1), С. 3 - 22
Опубликована: Дек. 30, 2023
Abstract
In
recent
years,
remarkable
breakthroughs
have
been
reported
on
antibody‐drug
conjugates
(ADCs),
with
15
ADCs
successfully
entering
the
market
over
past
decade.
This
substantial
development
has
positioned
as
one
of
fastest‐growing
domains
in
realm
anticancer
drugs,
demonstrating
their
efficacy
treating
a
wide
array
malignancies.
Nonetheless,
there
is
still
an
unmet
clinical
need
for
wider
application,
better
efficacy,
and
fewer
side
effects
ADCs.
An
ADC
generally
comprises
antibody,
linker
payload,
combination
profound
drug
structure,
pharmacokinetic
profile
efficacy.
Hence,
optimization
key
components
provides
opportunity
to
develop
higher
potency
effects.
this
review,
we
comprehensively
reviewed
current
prospects
ADC,
provided
analysis
marketed
ongoing
pipelines
globally
well
China,
highlighted
several
platforms
technologies
specific
different
pharmaceutical
enterprises
biotech
companies,
also
discussed
new
related
technologies,
possibility
next‐generation
directions
research.
Drug Resistance Updates,
Год журнала:
2023,
Номер
71, С. 101002 - 101002
Опубликована: Авг. 22, 2023
Adenocarcinoma
is
a
common
type
of
malignant
tumor,
originating
from
glandular
epithelial
cells
in
various
organs,
such
as
pancreas,
breast,
lung,
stomach,
colon,
rectus,
and
prostate.
For
patients
who
lose
the
opportunity
for
radical
surgery,
medication
available
to
provide
potential
clinical
benefits.
However,
drug
resistance
big
obstacle
obtain
desired
prognosis.
In
this
review,
we
summary
treatment
strategies
mechanisms
adenocarcinoma
different
including
pancreatic
cancer,
gastric
adenocarcinoma,
colorectal
lung
prostate
cancer.
Although
underlying
molecular
involved
vary
one
organ
other,
there
are
several
targets
that
universal
targeting
these
molecules
could
potentially
reverse
adenocarcinomas.
Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics,
Год журнала:
2024,
Номер
32(3), С. 503 - 515
Опубликована: Янв. 1, 2024
The
increasing
interest
in
RNA
modifications
has
significantly
advanced
epigenomic
and
epitranscriptomic
technologies.
This
study
focuses
on
the
immuno-oncological
impact
of
ALYREF
human
cancer
through
a
pan-cancer
analysis,
enhancing
understanding
this
gene's
role
cancer.
We
observed
differential
expression
between
tumor
normal
samples,
correlating
strongly
with
prognosis
various
cancers,
particularly
kidney
renal
papillary
cell
carcinoma
(KIRP)
liver
hepatocellular
(LIHC).
showed
negative
correlation
most
tumor-infiltrating
cells
lung
squamous
(LUSC)
lymphoid
neoplasm
diffuse
large
B-cell
lymphoma
(DLBC),
while
positive
correlations
were
noted
LIHC,
chromophobe
(KICH),
mesothelioma
(MESO),
KIRP,
pheochromocytoma
paraganglioma
(PARD),
glioma
(GBMLGG).
Additionally,
was
closely
associated
heterogeneity,
stemness
indices,
high
mutation
rate
TP53
across
these
cancers.
In
conclusion,
may
serve
as
an
oncogenic
biomarker
numerous
meriting
further
research
attention.
Journal of Controlled Release,
Год журнала:
2024,
Номер
378, С. 438 - 459
Опубликована: Дек. 21, 2024
Cancer
vaccines
are
promising
therapeutic
approaches
to
enhance
specific
T-cell
immunity
against
most
solid
tumors.
By
stimulating
anti-tumor
immunity,
clearing
minimal
residual
disease,
and
minimizing
adverse
effects,
these
target
tumor
cells
effective
when
combined
with
immune
checkpoint
blockade
or
other
immunotherapies.
However,
the
development
of
cell-based
faces
quality
issues
due
poor
immunogenicity,
heterogeneity,
a
suppressive
microenvironment,
ineffective
delivery
methods.
In
contrast,
extracellular
vesicles
(EVs),
naturally
released
by
cells,
considered
ideal
drug
carriers
vaccine
platforms.
EVs
offer
highly
organ-specific
targeting,
induce
broader
more
responses,
demonstrate
superior
tissue
ability.
The
EV
is
crucial
for
advancing
cancer
immunotherapy.
Compared
vaccines,
produced
under
Good
Manufacturing
Practices
(GMP)
advantages
such
as
high
safety,
ease
preservation
transport,
wide
range
sources.
This
review
summarizes
latest
research
findings
on
potential
applications
in
this
field.
It
also
highlights
novel
neoantigens
cancer.
Molecular & Cellular Oncology,
Год журнала:
2025,
Номер
12(1)
Опубликована: Март 3, 2025
Immunotherapy
options
for
microsatellite
stable
(MSS)
colorectal
cancer
are
currently
very
limited.
The
lack
of
detectably
unique
or
altered
immunogens
in
the
tumor
microenvironment
may
be
a
factor.
Radiation
and
chemotherapy
enhance
immunotherapy
by
increasing
cell
visibility
through
Major
Histocompatibility
Complex
I
(MHC
I)
expression.
To
investigate
this,
we
treated
MSS
microsatellite-instable
(MSI)
colon
cells
with
topoisomerase
inhibitor
analyzed
MHC
I-associated
peptides.
Treatment
increased
peptide
numbers
5%
RKO
83%
SW620
cells,
40-50%
peptides
being
exclusive
to
treatment.
Additionally,
clustering
analysis
revealed
set
uniquely
conserved
residues
displayed
only
cells.
Gene
Ontology
I-displayed
proteins
treatment-induced
increase
extracellular
vesicle-
nuclear-derived
proteins,
alongside
reduced
cytosolic
protein
sampling.
Overall,
present
evidence
treatment-inducible
differential
display
peptides,
some
which
affect
interactions
functions
immune
Given
multitude
factors
that
modulate
effects
expression
associated
further
studies
needed
elucidate
pathophysiological
implications
these
changes.
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(7), С. 2923 - 2923
Опубликована: Март 24, 2025
Understanding
the
modulation
of
specific
immune
cells
within
tumor
microenvironment
(TME)
offers
new
hope
in
cancer
treatments,
especially
immunotherapies.
In
recent
years,
and
resistance
to
immunotherapy
have
become
critical
challenges
treatments.
However,
novel
strategies
for
emerged
as
promising
approaches
oncology
due
vital
roles
immunomodulators
regulating
progression
metastasis
modulating
immunological
responses
standard
care
With
progress
immuno-oncology,
a
growing
number
mechanisms
are
being
uncovered,
offering
potential
enhanced
clinical
near
future.
Thus,
gaining
comprehensive
understanding
broader
context
is
essential.
Herein,
we
particularly
summarize
paradoxical
role
tumor-related
cells,
focusing
on
how
targeted
their
actions
modulated
by
immunotherapies
overcome
immunotherapeutic
cells.
We
also
highlight
molecular
employed
tumors
evade
long-term
effects
agents,
rendering
them
ineffective.
Exploration of Immunology,
Год журнала:
2025,
Номер
5
Опубликована: Апрель 8, 2025
Neoantigen
vaccines
are
a
promising
strategy
in
cancer
immunotherapy
that
leverage
tumor-specific
mutations
to
elicit
targeted
immune
responses.
Although
they
have
considerable
potential,
development
challenges
related
antigen
prediction
accuracy,
manufacturing
complexity,
and
scalability
remain
key
obstacles
their
widespread
clinical
use.
This
literature
review
was
conducted
using
PubMed,
Scopus,
Web
of
Science,
Google
Scholar
databases
identify
relevant
studies.
Keywords
included
“neoantigen
vaccines,”
“personalized
immunotherapy,”
“tumor
heterogeneity,”
“bioinformatics
pipelines,”
“prediction
algorithms”.
Clinical
trial
data
were
sourced
from
ClinicalTrials.gov,
Trialtrove,
other
publicly
available
registries.
Eligible
studies
peer-reviewed
research
articles,
systematic
reviews,
trials
focusing
on
neoantigen
vaccine
development,
bioinformatic
strategies,
immunotherapy.
Tumor
heterogeneity
clonal
evolution
significantly
impact
efficacy,
necessitating
multi-epitope
targeting
adaptive
design.
Current
algorithms
suffer
high
false-positive
false-negative
rates,
requiring
further
integration
with
multi-omics
machine
learning
enhance
accuracy.
Manufacturing
remains
complex,
time-intensive,
costly,
advancements
standardization
automation.
Combination
therapies,
such
as
checkpoint
inhibitors
adoptive
cell
counteract
the
immunosuppressive
tumor
microenvironment,
improving
treatment
outcomes.
hold
great
potential
for
personalized
therapy
but
require
bioinformatics,
scalability,
immunomodulatory
strategies
efficacy.
Continued
interdisciplinary
collaboration
essential
refining
applications.
Exploration of Targeted Anti-tumor Therapy,
Год журнала:
2025,
Номер
6
Опубликована: Апрель 27, 2025
Neoantigen-based
immunotherapy
has
emerged
as
a
transformative
approach
in
cancer
treatment,
offering
precision
medicine
strategies
that
target
tumor-specific
antigens
derived
from
genetic,
transcriptomic,
and
proteomic
alterations
unique
to
cells.
These
neoantigens
serve
highly
specific
targets
for
personalized
therapies,
promising
more
effective
tailored
treatments.
The
aim
of
this
article
is
explore
the
advances
neoantigen-based
highlighting
successful
treatments
such
vaccines,
tumor-infiltrating
lymphocyte
(TIL)
therapy,
T-cell
receptor-engineered
T
cells
therapy
(TCR-T),
chimeric
antigen
receptor
(CAR-T),
particularly
types
like
glioblastoma
(GBM).
Advances
technologies
next-generation
sequencing,
RNA-based
platforms,
CRISPR
gene
editing
have
accelerated
identification
validation
neoantigens,
moving
them
closer
clinical
application.
Despite
results,
challenges
tumor
heterogeneity,
immune
evasion,
resistance
mechanisms
persist.
integration
AI-driven
tools
multi-omic
data
refined
neoantigen
discovery,
while
combination
therapies
are
being
developed
address
issues
suppression
scalability.
Additionally,
discusses
ongoing
development
immunotherapies
targeting
mutations,
emphasizing
need
continued
collaboration
between
computational
experimental
approaches.
Ultimately,
cutting-edge
research
holds
potential
revolutionize
care,
hope
targeted
Dendritic
cells
(DCs)
are
critical
players
at
the
intersection
of
innate
and
adaptive
immunity,
making
them
ideal
candidates
for
anticancer
vaccine
development.
DC-based
immunotherapies
typically
involve
isolating
patient-derived
DCs,
pulsing
with
tumor-associated
antigens
(TAAs)
or
tumor-specific
(TSAs),
utilizing
maturation
cocktails
to
ensure
their
effective
activation.
These
matured
DCs
then
reinfused
elicit
T-cell
responses.
While
this
approach
has
demonstrated
ability
generate
potent
immune
responses,
its
clinical
efficacy
been
limited
due
immunosuppressive
tumor
microenvironment.
Recent
efforts
have
focused
on
enhancing
immunogenicity
vaccines,
particularly
through
combination
therapies
T
cell-targeting
immunotherapies.
This
Trial
Watch
summarizes
recent
advances
in
cancer
treatments,
including
development
new
preclinical
strategies,
discusses
future
potential
vaccines
evolving
landscape
immuno-oncology.