Recent Advancements, Limitations, and Future Perspectives of the use of Personalized Medicine in Treatment of Colon Cancer
Technology in Cancer Research & Treatment,
Год журнала:
2023,
Номер
22
Опубликована: Янв. 1, 2023
Due
to
the
heterogeneity
of
colon
cancer,
surgery,
chemotherapy,
and
radiation
are
ineffective
in
all
cases.
The
genomic
profile
biomarkers
associated
with
process
considered
personalized
medicine,
along
patient's
personal
history.
It
is
based
on
response
targeted
therapies
specific
genetic
variations.
transcriptomic
epigenetic
features
evaluated,
best
therapeutic
approach
diagnostic
testing
identified
through
medicine.
This
review
aims
summarize
necessary,
updated
information
cancer
related
Personalized
medicine
gaining
prominence
as
generalized
treatments
finding
it
challenging
contain
cases
which
currently
rank
fourth
among
global
incidence
while
being
fifth
largest
total
death
worldwide.
In
therapy,
patients
grouped
into
categories,
chosen
evaluating
their
molecular
features.
Various
strategies
explored
treatment
involving
immunotherapy,
phytochemicals,
other
biomarker-specific
therapies.
However,
significant
challenges
must
be
overcome
integrate
healthcare
systems
completely.
We
look
at
various
signaling
pathways
alterations
understand
identify
useful
therapy.
current
available
improve
existing
methods
discussed.
highlights
advantages
limitations
scenario
developed
countries
faced
middle-
low-income
also
summarized.
Finally,
we
discuss
future
perspectives
how
could
integrated
systems.
Язык: Английский
Harnessing the potential of HLA-G in cancer therapy: advances, challenges, and prospects
Journal of Translational Medicine,
Год журнала:
2024,
Номер
22(1)
Опубликована: Фев. 3, 2024
Abstract
Immune
checkpoint
blockades
have
been
prized
in
circumventing
and
ablating
the
impediments
posed
by
immunosuppressive
receptors,
reaching
an
exciting
juncture
to
be
innovator
anticancer
therapy
beyond
traditional
therapeutics.
Thus
far,
approved
immune
principally
targeted
PD-1/PD-L1
CTLA-4
with
success
a
plethora
of
tumors
yet
are
still
trapped
dilemmas
limited
response
rates
adverse
effects.
Hence,
unveiling
new
immunotherapeutic
targets
has
aroused
immense
scientific
interest
hope
expanding
clinical
application
scale
heights.
Human
leukocyte
antigen-G
(HLA-G),
non-classical
major
histocompatibility
complex
(MHC)
class
I
molecule,
is
enriched
on
various
malignant
cells
involved
hindrance
effector
facilitation
cells.
HLA-G
stands
out
as
crucial
next-generation
showing
great
promise
for
benefit
cancer
patients.
Here,
we
provide
overview
current
understanding
expression
pattern
immunological
functions
HLA-G,
well
its
interaction
well-characterized
checkpoints.
Since
can
shed
from
cell
surface
or
released
free
soluble
(sHLA-G)
part
extracellular
vesicles
(EVs),
namely
HLA-G-bearing
EVs
(HLA-G
EV
),
discuss
potential
sHLA-G
predictive
biomarkers.
This
review
also
addresses
advancement
HLA-G-based
therapies
preclinical
settings,
focus
their
cancer.
Язык: Английский
Immunotherapy for colorectal cancer: insight from inherited genetics
Trends in cancer,
Год журнала:
2024,
Номер
10(5), С. 444 - 456
Опубликована: Фев. 14, 2024
Язык: Английский
Exploring the Role of KIR2DS4 and HLA-A*02:07 in Predicting Chemotherapy Sensitivity and Erythrocytopenia in Nasopharyngeal Carcinoma
Research Square (Research Square),
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 11, 2025
Abstract
Background:
Nasopharyngeal
carcinoma
(NPC)
is
common
in
Southeast
Asia,
with
most
patients
diagnosed
locally
advanced
disease.
Radiotherapy
alone
often
ineffective,
so
platinum-based
chemotherapy
combined
for
better
outcomes.
However,
response
and
side
effects
vary
among
patients.
Genetic
markers,
particularly
human
leukocyte
antigen
(HLA)
killer-cell
immunoglobulin-like
receptors
(KIR),
have
been
implicated
modulating
sensitivity
toxicity.
Identifying
these
markers
could
facilitate
personalized
treatment
strategies
NPC
Methods:
This
study
included
204
between
April
2020
October
2021,
performed
KIR
HLA-A
allele
typing.
The
control
group
consisted
of
201
healthy
individuals,
matched
by
gender
age,
who
underwent
routine
health
check-ups
at
the
hospital.
Among
cases,
110
nasopharyngeal
received
platinum
based
were
analyzed
relationship
HLA
genotype
characteristics
sensitivity,
as
well
occurrence
induced
effects.
Results:
exhibited
higher
expression
activating
KIR2DS4
(97.55%
vs
91.54%,
OR
=
3.677,
95%
CI
1.320
~
10.168,
P
0.008)
inhibitory
KIR3DL1
93.03%,
2.980,
1.053
8.434,
P
0.032),
suggesting
their
involvement
BB
haplotype,
a
particular
gene
combination,
was
less
frequent
patients,
hinting
protective
effect
(4.90%
11.44%,
0.399,
0.185
0.861,
0.016).
detection
frequency
HLA-A*11:01
case
significantly
lower
than
that
(23.53%
30.71%,
0.694,
0.505
0.955,
0.024),
HLA-A*02:07
(17.16%
8.70%,
2.175,
1.394
3.392,
<
0.001).
Notably,
associated
increased
(51.35%
21.91%,
3.760,
1.552
8.648,
0.002).
Additionally,
KIR2DS4*003
linked
to
reduced
incidence
chemotherapy-induced
erythrocytopenia
(2.63%
97.37%
non-carriers,
0.135,
0.017
1.082,
0.032).
Conclusions:
Our
findings
suggest
are
promising
genetic
predicting
risk
These
results
support
potential
regimens
on
profiling,
helping
reduce
improve
efficacy.
Язык: Английский
Analysis of HLA-G 14 bp Insertion/Deletion Polymorphism and HLA-G, ILT2 and ILT4 Expression in Head and Neck Squamous Cell Carcinoma Patients
Diseases,
Год журнала:
2024,
Номер
12(2), С. 34 - 34
Опубликована: Фев. 8, 2024
HLA-G
is
the
checkpoint
molecule
involved
in
suppression
of
immune
response.
Increased
expression
and
its
ILTs
receptors
have
been
correlated
with
tumor
progression
various
cancer
types.
In
head
neck
squamous
cell
carcinoma
(HNSCC)
tumors,
effect
HLA-G,
ILT2
ILT4
on
development
has
to
be
explained.
The
34
HNSCC
patients
98
controls
were
genotyped
for
14
bp
ins/del
polymorphism.
lesions,
mRNA
was
analysed
using
real-time
PCR.
association
between
clinical
variables
(age
at
onset,
TNM
staging
system
p16
positivity)
also
evaluated.
No
genetic
risk
detected
(p
>
0.05).
However,
non-metastatic
group,
a
significantly
higher
noted
tumors
T4
stage
compared
those
T1
T2
stages
=
0.0289).
increased
vs.
metastatic
0.0269).
Furthermore,
T1+T2
T3
0.0495).
Our
results
suggest
that
creates
an
immunological
microenvironment
development.
Язык: Английский