Epigenomics,
Journal Year:
2023,
Volume and Issue:
15(4), P. 227 - 248
Published: Feb. 1, 2023
The
COVID-19
outbreak
has
created
disaster
globally,
and
mankind
is
yet
to
come
in
terms
with
combating
this
global
menace.
Amid
turmoil,
immunocompromised
individuals
like
cancer
patients
exhibit
dismal
immune
responses
toward
such
infection.
In
order
treat
during
adverse
situations,
it
necessary
understand
the
phenomena
that
interlink
these
two
diseased
states.
Modulation
of
host
epigenetic
landscape
a
key
hallmark
both
viral
infections,
including
COVID-19.
Our
review
aims
shed
light
upon
interplay
between
cancer,
primarily
through
genetic
modulations
gene
expression
profile,
so
as
design
better
therapeutic
strategies
near
future.
Advanced Materials,
Journal Year:
2022,
Volume and Issue:
35(17)
Published: Nov. 1, 2022
Abstract
Leukocytes
play
a
vital
role
in
immune
responses,
including
defending
against
invasive
pathogens,
reconstructing
impaired
tissue,
and
maintaining
homeostasis.
When
the
system
is
activated
vivo,
leukocytes
accomplish
series
of
orderly
complex
regulatory
processes.
While
cancer
inflammation‐related
diseases
like
sepsis
are
critical
medical
difficulties
plaguing
humankind
around
world,
have
been
shown
to
largely
gather
at
focal
site,
significantly
contribute
inflammation
progression.
Therefore,
living
leukocyte‐based
drug
delivery
systems
attracted
considerable
attention
recent
years
due
innate
specific
targeting
effect,
low
immunogenicity,
improved
therapeutic
efficacy,
reverse
effect.
In
this
review,
advances
development
macrophages,
neutrophils,
lymphocytes
as
promising
treatment
strategies
for
introduced.
The
advantages,
current
challenges,
limitations
these
also
discussed,
well
perspectives
on
future
precision
targeted
therapy
clinics
provided.
Collectively,
it
expected
that
such
kind
cell‐based
improve
or
even
revolutionize
treatments
cancers
clinics.
Cellular and Molecular Immunology,
Journal Year:
2023,
Volume and Issue:
20(7), P. 739 - 776
Published: May 17, 2023
Abstract
Over
the
past
thirty
years,
importance
of
chemokines
and
their
seven-transmembrane
G
protein-coupled
receptors
(GPCRs)
has
been
increasingly
recognized.
Chemokine
interactions
with
trigger
signaling
pathway
activity
to
form
a
network
fundamental
diverse
immune
processes,
including
host
homeostasis
responses
disease.
Genetic
nongenetic
regulation
both
expression
structure
conveys
chemokine
functional
heterogeneity.
Imbalances
defects
in
system
contribute
pathogenesis
variety
diseases,
cancer,
inflammatory
metabolic
neurological
disorders,
which
render
focus
studies
aiming
discover
therapies
important
biomarkers.
The
integrated
view
biology
underpinning
divergence
plasticity
provided
insights
into
dysfunction
disease
states,
including,
among
others,
coronavirus
2019
(COVID-19).
In
this
review,
by
reporting
latest
advances
results
from
analyses
plethora
sequencing-based
datasets,
we
outline
recent
understanding
genetic
variations
heterogeneity
provide
an
updated
contribution
pathophysiological
network,
focusing
on
chemokine-mediated
inflammation
cancer.
Clarification
molecular
basis
dynamic
chemokine-receptor
will
help
advance
achieve
precision
medicine
application
clinic.
Seminars in Cancer Biology,
Journal Year:
2021,
Volume and Issue:
85, P. 155 - 163
Published: July 24, 2021
Cancer
metastasis
is
a
major
reason
for
the
cancer-associated
deaths
and
role
of
long
non-coding
RNAs
(lncRNAs)
in
cancer
increasingly
being
realized.
Among
many
oncogenic
pathways,
NF-κB
signalling's
involvement
as
key
inflammation-regulatory
transcription
factor
has
been
subject
interest
time.
Accumulating
data
from
vitro
well
vivo
studies
along
with
analysis
clinical
tissues
points
to
regulation
signalling
by
lncRNAs
implications
toward
onset
metastasis.
LncRNAs
FOXD2-AS1,
KRT19P3
interacting
lncRNA
(NKILA)
associate
lymph
node
poor
prognosis
individual
cancers.
The
epithelial-mesenchymal
transition
(EMT)
known.
EMT
regulated
NF-κB/EMT-induced
remains
hot
topic
research
indications
such
roles
MALAT1,
SNHG15,
CRNDE
AC007271.3.
lncRNAs,
NKILA
stands
out
most
investigated
its
NF-κB.
This
tumor
suppressive
reported
downregulated
samples
representing
different
human
Mechanistically,
consistently
shown
inhibit
activation
via
inhibition
IκBα
phosphorylation
resulting
suppression
EMT.
also
target
natural
anticancer
compounds.
Given
importance
master
regulatory
factor,
modulators
signaling,
can
provide
alternate
targets
metastatic
cancers
constitutively
active
Seminars in Cancer Biology,
Journal Year:
2022,
Volume and Issue:
86, P. 697 - 708
Published: March 26, 2022
Signaling
involving
chemokine
receptor
CXCR4
and
its
ligand
SDF-1/CXL12
has
been
investigated
for
many
years
possible
role
in
cancer
progression
pathogenesis.
Evidence
emerging
from
clinical
studies
recent
further
established
diagnostic
as
well
prognostic
importance
of
signaling.
SDF-1
are
routinely
reported
to
be
elevated
tumors,
distant
metastases,
which
correlates
with
poor
survival
patients.
These
findings
have
kindled
interest
the
mechanisms
that
regulate
CXCR4/SDF-1
expression.
Of
note,
there
is
a
particular
epigenetic
regulation
signaling
may
responsible
upregulated
primary
metastatic
cancers.
This
review
first
lists
evidence
supporting
putative
and/or
biomarker,
followed
by
discussion
on
affect
include
non-coding
RNAs,
such
as,
microRNAs,
long
RNAs
circular
RNAs.
Additionally,
we
also
discuss
expression
through
methylation
acetylation.
Better
understanding
appreciation
can
invariably
lead
identification
novel
therapeutic
targets
therapies
this
oncogenic
Seminars in Cancer Biology,
Journal Year:
2023,
Volume and Issue:
92, P. 74 - 83
Published: April 11, 2023
Cancer
'stemness'
is
fundamental
to
cancer
existence.
It
defines
the
ability
of
cells
indefinitely
perpetuate
as
well
differentiate.
stem
cell
populations
within
a
growing
tumor
also
help
evade
inhibitory
effects
chemo-
radiation-therapies,
in
addition
playing
an
important
role
metastases.
NF-κB
and
STAT-3
are
representative
transcription
factors
(TFs)
that
have
long
been
associated
with
stemness,
thus
presenting
attractive
targets
for
therapy.
The
interest
non-coding
RNAs
(ncRNAs)
recent
years
has
provided
further
insight
into
mechanisms
by
which
TFs
influence
characteristics.
There
evidence
direct
regulation
ncRNAs,
such
as,
microRNAs
(miRNAs),
(lncRNAs)
circular
(circRNAs),
vice
versa.
Additionally,
TF-ncRNAs
regulations
often
indirect,
involving
ncRNA-target
genes
or
sponging
other
ncRNA
species
individual
ncRNAs.
information
rapidly
evolving
this
review
provides
comprehensive
interactions
implications
on
stemness
response
therapies.
Such
knowledge
will
uncover
many
levels
tight
control
providing
novel
opportunities
therapy
process.
International Journal of Molecular Sciences,
Journal Year:
2021,
Volume and Issue:
22(19), P. 10351 - 10351
Published: Sept. 26, 2021
A
high
incidence
of
thromboembolic
events
associated
with
mortality
has
been
reported
in
severe
acute
respiratory
syndrome
coronavirus
type
2
(SARS-CoV-2)
infections
failure.
The
present
study
characterized
post-transcriptional
gene
regulation
by
global
microRNA
(miRNA)
expression
relation
to
activated
coagulation
and
inflammation
21
critically
ill
SARS-CoV-2
patients.
cohort
consisted
patients
moderate
failure
(n
=
11)
10)
at
an
stage
(day
0-3)
the
later
course
disease
(>7
days).
All
needed
supplemental
oxygen
were
defined
requirement
positive
pressure
ventilation
(intubation).
Levels
D-dimers,
partial
thromboplastin
time
(aPTT),
C-reactive
protein
(CRP),
interleukin
(IL)-6
significantly
higher
compared
Concurrently,
next
generation
sequencing
(NGS)
analysis
demonstrated
increased
dysregulation
miRNA
progression
severity
connected
extreme
downregulation
miR-320a,
miR-320b
miR-320c.
Kyoto
encyclopedia
genes
genomes
(KEGG)
pathway
revealed
involvement
Hippo
signaling
pathway,
transforming
growth
factor
(TGF)-β
adherens
junctions.
all
miR-320
family
members
was
correlated
CRP,
IL-6,
D-dimer
levels.
In
conclusion,
our
underlines
importance
processes
emphasizes
miRNA-320s
as
potential
biomarkers
for
progressive
infection.
Seminars in Cell and Developmental Biology,
Journal Year:
2023,
Volume and Issue:
154, P. 199 - 207
Published: April 27, 2023
Atopic
dermatitis
(AD),
also
known
as
atopic
eczema,
is
a
common
but
complex
chronic,
itchy
skin
condition
with
underlying
inflammation
of
the
skin.
This
ailment
prevalent
worldwide
and
affects
people
all
ages,
particularly
children
below
five
years
age.
The
itching
resulting
rashes
in
AD
patients
are
often
result
inflammatory
signals,
thus
necessitating
closer
look
at
inflammation-regulating
mechanisms
for
putative
relief,
care
therapy.
Several
chemical-
well
genetically-induced
animal
models
have
established
importance
targeting
pro-inflammatory
microenvironment.
Epigenetic
gaining
attention
towards
better
understanding
onset
progression
inflammation.
physiological
processes
implications
pathophysiology
AD,
such
as,
barrier
dysfunction
either
due
to
reduced
filaggrin
/
human
β‐defensins
or
altered
microbiome,
reprograming
Fc
receptors
overexpression
high
affinity
IgE
receptors,
elevated
eosinophil
numbers
IL-22
production
by
CD4
+
T
cells
epigenetic
that
include
differential
promoter
methylation
and/or
regulation
non-coding
RNAs.
Reversing
these
changes
has
been
verified
reduce
burden
through
secretion
cytokines
IL-6,
IL-4,
IL-13,
IL-17,
etc,
benefit
against
experimental
models.
A
thorough
remodeling
potential
opening
avenues
novel
diagnostic,
prognostic
therapeutic
options.
Ecotoxicology and Environmental Safety,
Journal Year:
2024,
Volume and Issue:
271, P. 115980 - 115980
Published: Jan. 22, 2024
Epidemiologic
studies
have
reported
the
positive
relationship
of
benzo[a]pyrene
(BaP)
exposure
with
risk
lung
cancer.
However,
mechanisms
underlying
is
still
unclear.
Plasma
microRNA
(miRNA)
a
typical
epigenetic
biomarker
that
was
linked
to
environment
and
cancer
development.
We
aimed
reveal
mediation
effect
plasma
miRNAs
on
BaP-related
designed
case-control
study
including
136
patients
controls,
measured
adducts
diol
epoxide-albumin
(BPDE-Alb)
sequenced
miRNA
profiles
in
plasma.
The
relationships
between
BPDE-Alb
adducts,
normalized
levels
were
assessed
by
linear
regression
models.
effects
investigated.
A
total
190
significantly
related
status
at
Bonferroni
adjusted
P
<
0.05,
among
which
57
showed
different
|fold
change|
>
2
samples
before
after
tumor
resection
surgery
0.05.
Especially,
cancer-associated
miRNAs,
miR-17–3p,
miR-20a-3p,
miR-135a-5p,
miR-374a-5p,
miR-374b-5p,
miR-423–5p
miR-664a-5p,
could
turn
mediate
separate
42.2%,
33.0%,
57.5%,
36.4%,
48.8%,
32.5%
38.2%
Our
results
provide
non-invasion
candidates
for
cancer,
highlight
dysregulation
as
potential
intermediate
mechanism
BaP
lead
tumorigenesis.
Pharmaceutics,
Journal Year:
2024,
Volume and Issue:
16(5), P. 680 - 680
Published: May 17, 2024
Lung
diseases
have
received
great
attention
in
the
past
years
because
they
contribute
approximately
one-third
of
total
global
mortality.
Pulmonary
drug
delivery
is
regarded
as
one
most
appealing
routes
to
treat
lung
diseases.
It
addresses
numerous
drawbacks
linked
traditional
dosage
forms.
presents
notable
features,
such
as,
for
example,
a
non-invasive
route,
localized
delivery,
low
enzymatic
activity,
degradation,
higher
patient
compliance,
and
avoiding
first-pass
metabolism.
Therefore,
pulmonary
route
commonly
explored
delivering
drugs
both
locally
systemically.
Inhalable
nanocarrier
powders,
especially,
lipid
nanoparticle
formulations,
including
solid-lipid
nanostructured-lipid
nanocarriers,
are
attracting
considerable
interest
addressing
respiratory
thanks
their
significant
advantages,
deep
deposition,
biocompatibility,
biodegradability,
mucoadhesion,
controlled
released.
Spray
drying
scalable,
fast,
commercially
viable
technique
produce
nanolipid
powders.
This
review
highlights
ideal
criteria
inhalable
spray-dried
SLN
NLC
powders
administration
route.
Additionally,
promising
inhalation
devices,
known
dry
powder
inhalers
(DPIs)
powder-based
medications,
applications
treating
chronic
conditions,
considered.