Journal of Clinical Medicine,
Journal Year:
2024,
Volume and Issue:
13(19), P. 5876 - 5876
Published: Oct. 2, 2024
Head
and
neck
squamous
cell
carcinoma
(HNSCC)
is
the
sixth
most
common
cancer
worldwide,
characterized
by
high
aggressiveness
frequent
metastasis
to
regional
lymph
nodes.
Despite
advances
in
therapy,
including
checkpoint
inhibitor
immunotherapy,
surgery,
radiotherapy,
chemotherapy,
survival
rates
for
patients
with
advanced
HNSCC
remain
unsatisfactory.
This
article
presents
latest
research
on
predictive
biomarkers
such
as
PD-L1,
PD-1,
CTLA-4,
p53,
HPV,
which
may
enhance
treatment
efficacy
improve
clinical
outcomes
patients.
The
value
of
these
biomarkers,
their
limitations,
potential
application
therapy
are
emphasized.
Special
attention
given
shows
promising
results
treating
this
type
through
modulation
immune
response.
review’s
findings
highlight
need
further
new
develop
more
personalized
effective
therapeutic
strategies
Cancers,
Journal Year:
2022,
Volume and Issue:
14(24), P. 6079 - 6079
Published: Dec. 10, 2022
Head
and
neck
cancer
(HNC),
also
known
as
the
that
can
affect
structures
between
dura
mater
pleura,
is
6th
most
common
type
of
cancer.
This
heterogeneous
group
malignancies
usually
treated
with
a
combination
surgery
radio-
chemotherapy,
depending
on
if
disease
localized
or
at
an
advanced
stage.
However,
HNC
patients
are
diagnosed
stage,
resulting
in
death
half
these
patients.
Thus,
prognosis
recurrent/metastatic
HNC,
especially
squamous
cell
carcinoma
(HNSCC),
notably
poorer
than
HNC.
review
explores
epidemiology
etiologic
factors
histopathology
this
cancer,
diagnosis
methods
treatment
approaches
currently
available.
Moreover,
special
interest
given
to
novel
therapies
used
treat
subtypes
worse
prognosis,
exploring
immunotherapies
targeted/multi-targeted
drugs
undergoing
clinical
trials,
well
light-based
(i.e.,
photodynamic
photothermal
therapies).
Journal of Personalized Medicine,
Journal Year:
2022,
Volume and Issue:
12(6), P. 854 - 854
Published: May 24, 2022
Head
and
neck
cancers
(HNCs)
represent
the
sixth
most
widespread
malignancy
worldwide.
Surgery,
radiotherapy,
chemotherapeutic
immunotherapeutic
drugs
main
clinical
approaches
for
HNC
patients.
Moreover,
HNCs
are
characterised
by
an
elevated
mutational
load;
however,
specific
genetic
mutations
or
biomarkers
have
not
yet
been
found.
In
this
scenario,
personalised
medicine
is
showing
its
efficacy.
To
study
reliability
effects
of
treatments,
preclinical
research
can
take
advantage
next-generation
sequencing
innovative
technologies
that
developed
to
obtain
genomic
multi-omic
profiles
drive
treatments.
The
crosstalk
between
malignant
healthy
components,
as
well
interactions
with
extracellular
matrices,
important
features
which
responsible
treatment
failure.
Preclinical
has
constantly
implemented
in
vitro
vivo
models
mimic
natural
tumour
microenvironment.
Among
them,
3D
systems
reproduce
mass
architecture,
such
biomimetic
scaffolds
organoids.
addition,
changed
over
last
decades
overcome
problems
animal
management
complexity
time-consuming
experiments.
review,
we
will
explore
new
aimed
improve
tools
apply
precision
a
therapeutic
option
patients
affected
HNCs.
Expert Opinion on Biological Therapy,
Journal Year:
2023,
Volume and Issue:
23(11), P. 1053 - 1065
Published: Nov. 2, 2023
Introduction
In
the
field
of
bioconjugates,
focus
on
antibody
–
drug
conjugates
(ADCs)
with
novel
payloads
beyond
traditional
categories
potent
cytotoxic
agents
is
increasing.
These
innovative
ADCs
exhibit
various
molecular
formats,
ranging
from
small-molecule
payloads,
such
as
immune
agonists
and
proteolytic
agents,
to
macromolecular
oligonucleotides
proteins.
Molecular Carcinogenesis,
Journal Year:
2023,
Volume and Issue:
62(8), P. 1091 - 1106
Published: April 17, 2023
Aberrant
N7
-methylguanosine
(m7G)
levels
closely
correlate
with
tumor
genesis
and
progression.
NCBP2
EIF4E3
are
two
important
m7G-related
cap-binding
genes.
This
study
aimed
to
identify
the
relationship
between
EIF4E3/NCBP2
function
immunological
characteristics
of
head
neck
squamous
cell
carcinoma
(HNSCC).
Hierarchical
clustering
was
employed
in
classifying
HNSCC
patients
into
groups
based
on
expressions
EIF4E3.
The
differentially
expressed
genes
were
identified
groups,
GO
functional
enrichment
subsequently
performed.
Weighted
gene
co-expression
network
analysis
conducted
hub
related
expression
immunity.
differential
infiltration
immune
cells
response
immunotherapy
compared
groups.
Single-cell
sequence
trajectory
analyses
performed
predict
differentiation
display
each
state.
In
addition,
quantitative
real-time
PCR,
spatial
transcriptome
analysis,
transwell
assay,
western
blotting
verify
biological
EIF4E3/NCBP2.
Here,
group
A
showed
a
higher
lower
expression,
which
had
scores,
proportion
most
cells,
activities,
immunomodulatory
targets,
better
cancer
immunotherapy.
Besides,
56
molecules
notable
regulation
significance
identified.
risk
model
containing
17
prognostic
nomogram
successfully
established.
Moreover,
tissues
than
normal
tissues.
played
vital
role
monocytes.
Furthermore,
CCL4/CCL5
can
be
regulated
via
overexpression
knockdown.
Collectively,
affect
downstream
as
well
contexture
immunotherapy,
could
induce
"cold-to-hot"
transformation
patients.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: Feb. 13, 2024
Platinum-based
antitumor
drugs
are
broad-spectrum
agents
with
unique
mechanisms
of
action.
Combination
chemotherapy
regimens
based
on
platinum
commonly
used
in
cancer
treatment.
However,
these
can
cause
various
adverse
reactions
the
human
body
through
different
routes
administration,
including
reproductive
toxicity,
genetic
and
embryonic
developmental
toxicity.
Preventing
effects
is
crucial
to
enhance
patients'
quality
life
reduce
healthcare
costs.
This
article
discusses
types
history
active
compounds,
their
action,
potential
reproductive,
genetic,
text
explores
preventive
measures
animal
experimental
results.
Its
aim
provide
references
for
personalized
treatment
occupational
protection
when
using
drugs.
The
continuous
progress
science
technology,
along
deepening
medical
research,
suggests
that
application
will
broaden.
Therefore,
development
new
be
an
important
direction
future
research.
Cancer Medicine,
Journal Year:
2024,
Volume and Issue:
13(13)
Published: July 1, 2024
Abstract
Background
Cancer
utilizes
immunosuppressive
mechanisms
to
create
a
tumor
microenvironment
favorable
for
its
progression.
The
purpose
of
this
study
is
histologically
characterize
the
immunological
properties
oral
squamous
cell
carcinoma
(OSCC)
and
identify
key
molecules
involved
in
patient
prognosis.
Methods
First,
overlapping
differentially
expressed
genes
(DEGs)
were
screened
from
OSCC
transcriptome
data
public
databases.
Correlation
analysis
DEGs
with
known
immune‐related
identified
immune
OSCC.
Next,
stromal
patterns
classified
immunohistochemical
staining
was
performed
markers
(CD3,
CD4,
Foxp3,
CD8,
CD20,
CD68,
CD163),
programmed
death‐ligand
1
(PD‐L1),
guanylate
binding
protein
5
(GBP5)
resected
specimens
obtained
110
patients
who
underwent
resection.
Correlations
between
each
factor
their
prognostic
impact
analyzed.
Results
Among
novel
OSCC‐specific
(including
ADAMDEC1
,
CXCL9
CXCL13
DPT
GBP5
IDO1
PLA2G7
),
selected
as
target
gene.
Histopathologic
showed
that
multiple
T‐cell
subsets
CD20‐positive
cells
less
common
advanced
stages,
whereas
CD163‐positive
more
stages.
immature
type
pattern
category
associated
infiltration,
lower
expression
PD‐L1
cells,
stroma,
shorter
overall
survival
recurrence‐free
survival.
Expression
stroma
correlated
infiltration
tumors
cells.
Patients
low
high
had
significantly
longer
Conclusions
may
reflect
both
invasive
immunomodulatory
potentials
cancer‐associated
fibroblasts
has
been
suggested
potential
biomarker
predict
prognosis
therapeutic
efficacy
checkpoint
inhibitors.
Oral Diseases,
Journal Year:
2023,
Volume and Issue:
30(4), P. 2075 - 2083
Published: Sept. 13, 2023
Abstract
Objectives
To
determine
the
diagnostic
accuracy
of
long
non‐coding
RNA
“MALAT1”
measured
in
saliva
patients
with
oral
squamous
cell
carcinoma
(OSCC)
and
assess
salivary
expression
microRNA‐124,
which
MALAT1
targets.
Subjects
Methods
Forty
subjects
were
collected
a
consecutive
pattern
allocated
into
two
groups.
Group
A
included
20
OSCC,
while
B
healthy
subjects.
Salivary
microRNA
(miRNA)‐124
was
evaluated
study
groups
using
quantitative
real‐time
polymerase
chain
reaction
correlated
histopathological
examination
OSCC
Results
yielded
statistically
significant
higher
than
controls
lower
miRNA‐124
controls.
There
is
inverse
relationship
between
miRNA‐124.
Moreover,
there
difference
samples
from
metastatic
cases
compared
non‐metastatic
cases,
as
well
lymph
node
involvement
those
without
involvement.
At
cut‐off
value
2.24,
exhibited
95%
sensitivity
90%
specificity
differentiating
Conclusion
acts
sponge
for
could
be
potential
biomarker
OSCC.