Biomedicine & Pharmacotherapy,
Journal Year:
2021,
Volume and Issue:
136, P. 111240 - 111240
Published: Jan. 19, 2021
The
extracellular
matrix
(ECM)
creates
a
multifaceted
system
for
the
interaction
of
diverse
structural
proteins,
matricellular
molecules,
proteoglycans,
hyaluronan,
and
various
glycoproteins
that
collaborate
bind
with
each
other
to
produce
bioactive
polymer.
Alterations
in
composition
configuration
ECM
elements
influence
cellular
phenotype,
thus
participating
pathogenesis
several
human
disorders.
Recent
studies
indicate
crucial
roles
non-coding
RNAs
modulation
ECM.
Several
miRNAs
such
as
miR-21,
miR-26,
miR-19,
miR-140,
miR-29,
miR-30,
miR-133
have
been
dysregulated
disorders
are
associated
disruption
or
breakdown
Moreover,
expression
MALAT1,
PVT1,
SRA1,
n379519,
RMRP,
PFL,
TUG1,
TM1P3,
FAS-AS1,
PART1,
XIST,
lncRNAs
is
altered
modification
components.
In
current
review,
we
discuss
role
their
relevance
pathophysiology
cardiac/
lung
fibrosis,
cardiomyopathy,
heart
failure,
asthma,
osteoarthritis,
cancers.
Acta Pharmaceutica Sinica B,
Journal Year:
2021,
Volume and Issue:
11(9), P. 2768 - 2782
Published: April 28, 2021
Pyroptosis
is
the
process
of
inflammatory
cell
death.
The
primary
function
pyroptosis
to
induce
strong
responses
that
defend
host
against
microbe
infection.
Excessive
pyroptosis,
however,
leads
several
diseases,
including
sepsis
and
autoimmune
disorders.
can
be
canonical
or
noncanonical.
Upon
infection,
pathway
responds
pathogen-associated
molecular
patterns
(PAMPs)
damage-associated
(DAMPs),
while
noncanonical
intracellular
lipopolysaccharides
(LPS)
Gram-negative
bacteria.
last
step
requires
cleavage
gasdermin
D
(GsdmD)
at
D275
(numbering
after
human
GSDMD)
into
N-
C-termini
by
caspase
1
in
4/5/11
(caspase
4/5
humans,
11
mice)
pathway.
cleavage,
N-terminus
GsdmD
(GsdmD-N)
forms
a
transmembrane
pore
releases
cytokines
such
as
IL-1β
IL-18
disturbs
regulation
ions
water,
eventually
resulting
inflammation
Since
effector
promising
inhibitors
have
been
developed
for
diseases.
This
review
will
focus
on
roles
during
Biotechnology and Applied Biochemistry,
Journal Year:
2021,
Volume and Issue:
69(1), P. 248 - 264
Published: Jan. 15, 2021
Autophagy
causes
the
breakdown
of
damaged
proteins
and
organelles
to
their
constituent
components.
The
phosphatidylinositol
3-kinase
(PI3K)
pathway
played
an
important
role
in
regulating
autophagic
response
cells
changing
reactive
oxygen
species
(ROS)
levels.
PI3K
α
catalytic
subunit
inhibits
autophagy,
while
its
β
promotes
autophagy
changes
ROS
downstream
Akt
protein
acts
against
initiation
increases
levels
under
nutrient-rich
conditions.
by
activating
a
mechanistic
target
rapamycin
complex
1
(mTORC1)
arresting
gene
expression.
AMP-activated
kinase
(AMPK)
counteracts
actions.
mTORC1
mTORC2
inhibit
moderate
levels,
but
high
can
promote
cellular
senescence
via
autophagy.
Phosphatase
tensin
homolog
(PTEN)
are
negative
regulators
pathway,
it
has
proautophagic
activities.
Studies
conducted
on
treated
with
flavonoids
ionizing
radiation
showed
that
increase
flavonoid-treated
groups
corresponded
higher
PTEN
lowered
leading
occurrence
In
contrast,
evoked
caused
lowering
incidence
Acta Pharmaceutica Sinica B,
Journal Year:
2020,
Volume and Issue:
11(4), P. 941 - 960
Published: Dec. 31, 2020
The
initiation
and
development
of
major
inflammatory
diseases,
i.e.,
cancer,
vascular
inflammation,
some
autoimmune
diseases
are
closely
linked
to
the
immune
system.
Biologics-based
immunotherapy
is
exerting
a
critical
role
against
these
whereas
usage
immunomodulators
always
limited
by
various
factors
such
as
susceptibility
digestion
enzymes
in
vivo,
poor
penetration
across
biological
barriers,
rapid
clearance
reticuloendothelial
Drug
delivery
strategies
potent
promote
their
delivery.
Herein,
we
reviewed
potential
targets
for
discussed
biologics
drug
systems
involved
immunotherapy,
particularly
highlighted
approved
therapy
tactics,
finally
offer
perspectives
this
field.
Cancer and Metastasis Reviews,
Journal Year:
2021,
Volume and Issue:
41(1), P. 53 - 75
Published: Oct. 23, 2021
Abstract
In
patients
with
glioblastoma,
the
average
survival
time
current
treatments
is
short,
mainly
due
to
recurrences
and
resistance
therapy.
This
insufficient
treatment
success
is,
in
large
parts,
tremendous
molecular
heterogeneity
of
gliomas,
which
affects
overall
prognosis
response
therapies
plays
a
vital
role
gliomas’
grading.
addition,
tumor
microenvironment
major
player
for
glioma
development
Active
communication
between
cells
local
or
neighboring
healthy
immune
environment
promotes
cancerogenic
processes
contributes
establishing
stem
cells,
drives
therapy
resistance.
Besides
genetic
alterations
primary
tumor,
tumor-released
factors,
cytokines,
proteins,
extracellular
vesicles,
environmental
influences
like
hypoxia
provide
ability
evade
host
surveillance
machinery
promote
disease
progression.
Moreover,
there
increasing
evidence
that
these
players
affect
biological
properties
gliomas
enable
inter-cell
supports
pro-cancerogenic
cell
properties.
Identifying
characterizing
complex
mechanisms
are
inevitably
necessary
adapt
therapeutic
strategies
develop
novel
measures.
Here
we
an
update
about
junctions
where
constant
traffic
biomolecules
adds
complexity
management
glioblastoma.
Graphical
abstract
Journal of Advanced Research,
Journal Year:
2021,
Volume and Issue:
37, P. 267 - 278
Published: Aug. 11, 2021
Elderly
population
has
been
progressively
rising
in
the
world,
thus
demand
for
anti-aging
heath
products
to
assure
longevity
as
well
ameliorate
age-related
complications
is
also
on
rise.
Among
various
health
products,
nicotinamide
mononucleotide
(NMN)
gaining
attentions
of
consumers
and
scientific
community.This
article
intends
provide
an
overview
current
knowledge
promises
safety
concerns
NMN
product.Nicotinamide
adenine
dinucleotide
(NAD+)
levels
body
deplete
with
aging
it
associated
downregulation
energy
production
mitochondria,
oxidative
stress,
DNA
damage,
cognitive
impairment
inflammatory
conditions.
However,
NMN,
precursor
NAD+,
can
slow
down
this
process
by
elevating
NAD+
body.
A
number
vivo
studies
have
indicated
affirmative
results
therapeutic
effects
age-induced
supplementation.
One
preclinical
one
clinical
study
conducted
investigate
administration
while
a
few
more
human
trials
are
being
conducted.
As
there
large
influx
based
market,
proper
investigations
urgently
needed
find
out
effectiveness
Biomedicine & Pharmacotherapy,
Journal Year:
2021,
Volume and Issue:
143, P. 112132 - 112132
Published: Sept. 1, 2021
Fibrosis
is
the
endpoint
of
pathological
remodeling.
This
process
contributes
to
pathogenesis
several
chronic
disorders
and
aging-associated
organ
damage.
Different
molecular
cascades
contribute
this
process.
TGF-β,
WNT,
YAP/TAZ
signaling
pathways
have
prominent
roles
in
A
number
long
non-coding
RNAs
microRNAs
been
found
regulate
fibrosis
through
modulation
activity
related
pathways.
miR-144-3p,
miR-451,
miR-200b,
miR-328
are
among
that
participate
pathology
cardiac
fibrosis.
Meanwhile,
miR-34a,
miR-17-5p,
miR-122,
miR-146a,
miR-350
liver
different
situations.
PVT1,
MALAT1,
GAS5,
NRON,
PFL,
MIAT,
HULC,
ANRIL,
H19
We
review
impact
aging-related
pathologies.
Journal of Clinical Investigation,
Journal Year:
2022,
Volume and Issue:
132(4)
Published: Feb. 14, 2022
The
importance
of
the
microbiota
in
development
colorectal
cancer
(CRC)
is
increasingly
evident,
but
identifying
specific
microbial
features
that
influence
CRC
initiation
and
progression
remains
a
central
task
for
investigators.
Studies
determining
mechanisms
directly
contribute
to
or
are
revealing
bacterial
factors
such
as
toxins
carcinogenesis.
However,
even
when
investigators
have
identified
bacteria
express
toxins,
questions
remain
about
host
determinants
toxin's
cancer-potentiating
effects.
For
other
cancer-correlating
lack
challenge
define
cancer-relevant
virulence
factors.
Herein,
we
evaluate
three
CRC-correlating
bacteria,
colibactin-producing
Escherichia
coli,
enterotoxigenic
Bacteroides
fragilis,
Fusobacterium
nucleatum,
their
relevant
CRC.
We
also
consider
beneficial
bioactivity
gut
microbes
by
highlighting
metabolite
may
enhance
antitumor
immunity.
In
doing
so,
aim
elucidate
unique
shared
underlying
microbiota's
contributions
accelerate
investigation
from
target
validation
therapeutic
discovery.
Advanced Science,
Journal Year:
2023,
Volume and Issue:
10(15)
Published: March 23, 2023
Abstract
Gut
microbiota‐derived
metabolites
are
key
hubs
connecting
the
gut
microbiome
and
cancer
progression,
primarily
by
remodeling
tumor
microenvironment
regulating
signaling
pathways
in
cells
multiple
immune
cells.
The
use
of
microbial
radiotherapy
chemotherapy
mitigates
severe
side
effects
from
treatment
improves
efficacy
treatment.
Immunotherapy
combined
with
effectively
activates
system
to
kill
tumors
overcomes
drug
resistance.
Consequently,
various
novel
strategies
have
been
developed
modulate
metabolites.
Manipulation
genes
involved
metabolism
using
synthetic
biology
approaches
directly
affects
levels
metabolites,
while
fecal
transplantation
phage
affect
altering
composition
microbiome.
However,
some
harbor
paradoxical
functions
depending
on
context
(e.g.,
type
cancer).
Furthermore,
metabolic
microorganisms
certain
anticancer
drugs
such
as
irinotecan
gemcitabine,
render
ineffective
or
exacerbate
their
adverse
effects.
Therefore,
a
personalized
comprehensive
consideration
patient's
condition
is
required
when
employing
treat
cancer.
purpose
this
review
summarize
correlation
between
cancer,
provide
fresh
ideas
for
future
scientific
research.
Acta Pharmaceutica Sinica B,
Journal Year:
2021,
Volume and Issue:
11(10), P. 3015 - 3034
Published: Feb. 26, 2021
Parkinson's
disease
(PD),
known
as
one
of
the
most
universal
neurodegenerative
diseases,
is
a
serious
threat
to
health
elderly.
The
current
treatment
has
been
demonstrated
relieve
symptoms,
and
discovery
new
small-molecule
compounds
regarded
promising
strategy.
Of
note,
homeostasis
autolysosome
pathway
(ALP)
closely
associated
with
PD,
impaired
autophagy
may
cause
death
neurons
thereby
accelerating
progress
PD.
Thus,
pharmacological
targeting
drawn
rising
attention
so
far.
In
this
review,
we
focus
on
summarizing
several
autophagy-associated
targets,
such
AMPK,
mTORC1,
ULK1,
IMPase,
LRRK2,
beclin-1,
TFEB,
GCase,
ERRα,
C-Abelson,
well
their
relevant
in
PD
models,
which
will
shed
light
clue
exploiting
more
potential
targeted
drugs
tracking
near
future.