Asian Journal of Medicine and Biomedicine,
Journal Year:
2023,
Volume and Issue:
7(2), P. 173 - 198
Published: Oct. 20, 2023
Despite
of
the
advancements
in
treating
cancer,
it
is
yet
one
dominant
causes
death
worldwide.
The
current
therapies
are
either
incapable
against
certain
cancers
or
impeding
to
patients,
which
diminishes
their
personal
satisfaction.
utilization
nanoparticles
cancer
treatment
might
possibly
increment
patient
endurance,
decrease
secondary
effects
and
diminish
rates.
fundamental
constraint
therapeutics
an
absence
explicitness
conveyance
as
they
target
normal
cells
too.
advancement
nanoscale
carriers
can
defeat
both
growth
hindrances
well
give
explicit,
designated
conveyance.
This
study
also
aims
focus
on
therapeutic
strategies
different
types
have
been
discussed
comprehensively.
Moreover,
nanomedicines
addressed
end
highlight
some
more
possible
measures.
Cancer Cell International,
Journal Year:
2023,
Volume and Issue:
23(1)
Published: Nov. 20, 2023
Abstract
Carcinoma
of
the
lung
is
among
most
common
types
cancer
globally.
Concerning
its
histology,
it
categorized
as
a
non-small
cell
carcinoma
(NSCLC)
and
small
(SCLC)
subtype.
MicroRNAs
(miRNAs)
are
member
non-coding
RNA
whose
nucleotides
range
from
19
to
25.
They
known
be
critical
regulators
via
epigenetic
control
oncogenes
expression
by
regulating
tumor
suppressor
genes.
miRNAs
have
an
essential
function
in
tumorous
microenvironment
modulating
growth,
metastasis,
angiogenesis,
metabolism,
apoptosis.
Moreover,
wide
information
produced
several
investigations
indicates
their
tumor-suppressing,
oncogenic,
diagnostic
assessment,
predictive
marker
functions
different
malignancy.
miRNA
mimics
or
anti-miRNAs
can
transferred
into
cell,
with
possible
curative
implications.
As
result,
hold
promise
targets
for
treatment
detection.
In
this
study,
we
investigate
various
malignancy,
which
been
achieved
recent
years
that
show
cancer-associated
regulation
expression,
concerning
beginning,
development,
resistance
chemotherapy,
also
probability
utilize
biomarkers
therapy
reaction.
Graphical
abstract
Cancers,
Journal Year:
2024,
Volume and Issue:
16(5), P. 923 - 923
Published: Feb. 25, 2024
Extracellular
vesicles
(EVs),
including
exosomes
and
microvesicles,
together
with
apoptotic
bodies
form
a
diverse
group
of
nanoparticles
that
play
crucial
role
in
intercellular
communication,
participate
numerous
physiological
pathological
processes.
In
the
context
cancer,
they
can
allow
transfer
bioactive
molecules
genetic
material
between
cancer
cells
surrounding
stromal
cells,
thus
promoting
such
processes
as
angiogenesis,
metastasis,
immune
evasion.
this
article,
we
review
recent
advances
understanding
how
EVs,
especially
exosomes,
influence
tumor
progression
modulation
microenvironment.
The
key
mechanisms
include
inducing
epithelial-mesenchymal
transition,
polarizing
macrophages
toward
protumoral
phenotypes,
suppressing
antitumor
immunity.
therapeutic
potential
engineered
is
highlighted,
their
loading
drugs,
RNA
therapeutics,
or
antigens
to
alter
Current
techniques
for
isolation,
characterization,
engineering
are
discussed.
Ongoing
challenges
improving
exosome
efficiency,
optimizing
biodistribution,
enhancing
selective
cell
targeting.
Overall,
present
promising
opportunities
understand
tumorigenesis
develop
more
targeted
diagnostic
strategies
by
exploiting
natural
communication
networks
tumors.
oncology,
regulatory
therapy
provides
possibility
reproducing
original
conditions
unfavorable
existence
process
may
be
feasible
alternative
population
treatments.
We
also
current
access
technology
enabling
intervention
using
exosomes.
International Journal of Molecular Sciences,
Journal Year:
2022,
Volume and Issue:
24(1), P. 93 - 93
Published: Dec. 21, 2022
Lung
cancer
(LC)
is
the
leading
cause
of
death
in
United
States.
Erythropoietin-producing
hepatocellular
receptors
(EPHs)
comprise
largest
receptor
tyrosine
kinases
(RTKs)
family
mammals.
EPHs
along
with
their
ligands,
EPH-family
receptor-interacting
proteins
(ephrins),
have
been
found
to
be
either
up-
or
downregulated
LC
cells,
hence
exhibiting
a
defining
role
carcinogenesis
and
tumor
progression.
In
capacity
as
membrane-bound
molecules,
EPHs/ephrins
may
represent
feasible
targets
context
precision
treatment.
order
investigate
available
therapeutics
targeting
EPH/ephrin
system
LC,
literature
review
was
conducted,
using
MEDLINE,
LIVIVO,
Google
Scholar
databases.
EPHA2
most
well-studied
target
The
EPHA2,
EPHA3,
EPHA5,
EPHA7,
EPHB4,
EPHB6,
ephrin-A1,
ephrin-A2,
ephrin-B2,
ephrin-B3
cells
xenograft
models
not
only
directly
correlates
profound
suppression
but
also
enriches
effects
well-established
therapeutic
regimens.
However,
sole
clinical
trial
incorporating
NSCLC
patient
could
describe
objective
anti-cancer
after
anti-EPHA2
antibody
administration.
Collectively,
seem
promising
treatment
LC.
large
trials
still
need
performed,
view
examining
setting.
Cancers,
Journal Year:
2022,
Volume and Issue:
15(1), P. 54 - 54
Published: Dec. 22, 2022
Inflammation
of
the
human
lung
is
mediated
in
response
to
different
stimuli
(e.g.,
physical,
radioactive,
infective,
pro-allergenic,
or
toxic)
such
as
cigarette
smoke
and
environmental
pollutants.
These
often
promote
an
increase
inflammatory
activities
airways,
manifesting
themselves
chronic
diseases
allergic
airway
diseases,
asthma
bronchitis/chronic
obstructive
pulmonary
disease,
even
cancer).
Non-coding
RNA
(ncRNAs)
are
single-stranded
molecules
few
nucleotides
that
regulate
gene
expression
involved
many
cellular
processes.
ncRNA
typically
reduction
translation
stability
genes
mRNAs
s.
They
biological
aspects
growth,
proliferation,
differentiation,
regulation
cell
cycle,
aging,
apoptosis,
metabolism,
neuronal
patterning,
influence
a
wide
range
biologic
processes
essential
for
maintenance
homeostasis.
The
relevance
ncRNAs
pathogenetic
mechanisms
respiratory
has
been
widely
established
last
decade
papers
were
published.
However,
once
their
importance
mechanisms,
it
becomes
important
further
deepen
research
this
direction.
In
review
we
describe
several
most
recent
knowledge
concerning
(overall
miRNAs)
lung.
Deleted Journal,
Journal Year:
2024,
Volume and Issue:
34(2), P. 241 - 250
Published: June 1, 2024
Aim:
The
purpose
of
our
study
was
to
investigate
the
impact
miR-137
suppression
on
growth
OECM-1
human
tongue
SCC
cell
line.
In
addition,
by
targeting
NF-Y
gene,
we
also
studied
molecular
mechanism
miR-137.
Methods:
(OECM-1)
&
negative
control
(SCC-15)
cells
were
transfected
with
microRNA137
inhibitor,
MTT
assay
utilized
ascertain
cytotoxic
impact.
SYBER
green-based
quantitative
polymerase
chain
reaction
used
determine
expression
level
both
and
genes
in
treated
untreated
cells.
collected
data
subjected
One-way
analysis
variance
(ANOVA)
Tukey's
multiple
comparisons
test.RESULTS:
According
research,
an
inhibitor
significantly
increased
their
ability
proliferate
when
compared
samples
control.
Also,
reported
that
is
down
regulated
OSCC
associated
1.4
folds
increase
cells.CONCLUSION:
MiR-137
lines
normal
its
inhibition
has
a
significant
proliferation
which
reflects
tumor
suppressor
role
OSCC.
marked
suggested
new
target
for
Authorea (Authorea),
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 16, 2024
Recent
advancements
in
immunotherapy
spotlight
the
pivotal
role
of
macrophages
disease
treatment.
The
polarization
macrophages,
wherein
these
immune
cells
differentiate
into
either
pro-inflammatory
(M1)
or
anti-inflammatory
(M2)
states,
plays
a
vital
therapeutic
modulation
spectrum
diseases.
Oligonucleotides
have
emerged
as
potent
tools
for
modulating
macrophage
with
high
specificity
and
potential
cost-effectiveness
compared
to
traditional
therapies.
In
this
review,
we
delve
application
oligonucleotides
steering
polarization,
introducing
how
is
polarized
4
different
kinds
oligonucleotide
(ASO,
siRNA,
agomir/antagomir
aptamer)
works,
discusses
their
potentials
challenges
associated
strategies,
emphasizing
importance
precise,
disease-specific
interventions
by
presenting
actual
examples.
While
clinical
faces
challenges,
also
highlights
some
recent,
significant
advances
current
trials
future
stimulating
advantages
immunotherapy,
signaling
frontier
treatment
management.