Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Sept. 9, 2024
Heparan
sulfate
proteoglycans
(HSPGs)
regulate
a
wide
range
of
biological
activities
in
both
physiological
and
pathological
conditions.
Altered
expression
or
deregulated
function
HSPGs
their
heparan
(HS)
chains
significantly
contribute
to
carcinogenesis
as
well
crucially
depends
on
the
functioning
complex
system
HS
biosynthetic/modifying
enzymes
termed
“GAGosome”.
Here,
we
aimed
at
investigating
profile
cell
culture
model
stroma-epithelial
crosstalk
searching
for
transcription
factors
potentially
related
regulation
genes
involved.
Coculture
BjTERT-fibroblasts
with
normal
PNT2
human
prostate
epithelial
cells
resulted
significant
downregulation
(2-4-fold)
transcriptional
activity
metabolism-involved
(
EXT1/2,
NDST1/2,
GLCE,
HS2ST1,
HS3ST1/2,
HS6ST1/2,
SULF1/2,
HPSE
)
types,
whereas
coculture
cancer
(LNCaP,
PC3,
DU145)
demonstrated
no
interchanges.
Human
Transcription
Factor
RT
2
Profiler
PCR
array
manual
RT-PCR
verification
supposed
FOS,
MYC,
E2F,
SRF,
NR3C1
potential
candidates
and/or
coordination
biosynthesis.
Taken
together,
biosynthetic
fibroblasts
during
might
be
controlled
by
intercellular
communication,
reflecting
adaptation
these
each
other.
The
is
attenuated
abrogated
if
interact
making
independent
limiting
effects
fibroblasts,
thus
contributing
possibility
unlimited
growth
progression.
Overall,
data
demonstrate
an
ability
cell-cell
interactions
affect
biosynthesis-involved
genes.
Biomolecules,
Journal Year:
2024,
Volume and Issue:
14(9), P. 1186 - 1186
Published: Sept. 20, 2024
Glycosaminoglycans
(GAGs)
and
proteoglycans
(PGs)
are
essential
components
of
the
extracellular
matrix
(ECM)
with
pivotal
roles
in
cellular
mechanosensing
pathways.
GAGs,
such
as
heparan
sulfate
(HS)
chondroitin
(CS),
interact
various
cell
surface
receptors,
including
integrins
receptor
tyrosine
kinases,
to
modulate
responses
mechanical
stimuli.
PGs,
comprising
a
core
protein
covalently
attached
GAG
chains,
serve
dynamic
regulators
tissue
mechanics
behavior,
thereby
playing
crucial
role
maintaining
homeostasis.
Dysregulation
GAG/PG-mediated
pathways
is
implicated
numerous
pathological
conditions,
cancer
inflammation.
Understanding
intricate
mechanisms
by
which
GAGs
PGs
forces
holds
promise
for
developing
novel
therapeutic
strategies
targeting
mechanotransduction
disease.
This
comprehensive
overview
underscores
importance
key
mediators
homeostasis
their
potential
targets
mitigating
mechano-driven
pathologies,
focusing
on
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(3), P. 1256 - 1256
Published: Jan. 31, 2025
Normal
development
of
joints
starts
in
utero
with
the
establishment
a
cellular
and
extracellular
matrix
template.
Following
birth,
individual
joint
tissues
grow
mature
response
to
biochemical
mechanical
signals,
leading
coordinated
pattern
further
maturation
resulting
that
functions
as
an
organ
system.
Each
develops
matures
system
defined
by
biomechanical
environment
which
it
will
function.
For
those
hypermobility
syndromes,
either
specific
genetic
mutations
or
not
(i.e.,
Ehlers–Danlos
syndrome,
Marfan
Loey–Dietz
hypermobility-type
syndrome),
this
process
is
partially
compromised,
but
many
aspects
tissue
function
retained
such
organs
form
retain
partial
function,
compromised.
Comparing
characteristics
what
known
regarding
development,
growth,
maturation,
stressors
puberty,
pregnancy,
aging
without
leads
conclusion
have
systems
may
be
compromised
via
failure
undergo
possibly
defective
mechanotransduction.
Given
breadth
involved
characterization
concept
reveal
commonalities
their
impact
on
inform
regulatory
normal
functional
integrity.
This
review/perspective
piece
attempt
detail
comparisons
summarize
how
study
aid
understanding.
Cells,
Journal Year:
2024,
Volume and Issue:
13(14), P. 1203 - 1203
Published: July 16, 2024
Hyaluronan
(HA)
is
a
large
polysaccharide
that
broadly
distributed
and
highly
abundant
in
the
soft
connective
tissues
embryos
of
vertebrates.
The
constitutive
turnover
HA
very
high,
estimated
at
5
g
per
day
an
average
(70
kg)
adult
human,
but
must
also
be
tightly
regulated
some
processes.
Six
genes
encoding
homologues
to
bee
venom
hyaluronidase
(
FEBS Journal,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 7, 2025
The
FEBS
Journal
editorial
team
reviews
the
articles
we
published
in
2024
and
reflects
on
year's
highlights.
summarised
here
broadly
cluster
three
themes—molecular
cell
biology
across
species,
immunology,
cutting‐edge
methods—whilst
still
showcasing
diversity
of
scientific
fields
journal
covers.
We
look
forward
to
many
more
excellent
2025
hope
these
highlights
will
inspire
you
submit
your
next
manuscript
Journal.
Proteoglycan Research,
Journal Year:
2025,
Volume and Issue:
3(1)
Published: Jan. 1, 2025
Solid
tumors
present
a
formidable
challenge
in
oncology,
necessitating
innovative
approaches
to
improve
therapeutic
outcomes.
Proteoglycans,
multifaceted
molecules
within
the
tumor
microenvironment,
have
garnered
attention
due
their
diverse
roles
cancer
progression.
Their
unique
ability
interact
with
specific
membrane
receptors,
growth
factors,
and
cytokines
provides
promising
avenue
for
development
of
recombinant
proteoglycan-based
therapies
that
could
enhance
precision
efficacy
treatment.
In
this
study,
we
performed
comprehensive
analysis
proteoglycan
gene
landscape
human
breast
carcinomas.
Leveraging
available
wealth
genomic
clinical
data
regarding
expression
carcinoma
using
machine
learning
model,
identified
signature
composed
five
proteoglycans
differentially
modulated
tissue:
Syndecan-1
asporin
(upregulated)
decorin,
PRELP
podocan
(downregulated).
Additional
query
revealed
serglycin,
previously
shown
be
increased
patients
mouse
models
correlate
poor
prognosis,
was
indeed
decreased
vast
majority
its
levels
inversely
correlated
progression
invasion.
This
provide
novel
diagnostic
capabilities
biology
highlights
need
further
utilization
publicly
datasets
validation
preclinical
experimental
results.
Macromolecular Bioscience,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 21, 2025
Abstract
Glycosaminoglycans
(GAGs)
play
a
pivotal
role
in
pathogen
attachment
and
entry
into
host
cells,
where
the
interaction
with
GAGs
is
critical
for
diverse
range
of
bacteria
viruses.
This
study
focuses
on
elucidating
specific
interactions
between
sulfated
adhesin
OmcB
(Outer
membrane
complex
protein
B)
Chlamydia
species,
examining
how
structural
characteristics
GAGs,
such
as
sulfation
degree
molecular
weight,
influence
their
binding
affinity
thereby
affect
bacterial
infectivity.
A
surface‐based
assay
established
to
determine
constants
various
GAGs.
It
shown
that
increased
higher
weight
enhance
GAG
OmcB.
These
findings
are
further
validated
using
cell
assays,
which
shows
addition
reduces
OmcB‐cell
inhibits
C.
pneumoniae
elementary
bodies
(EBs),
underscoring
chlamydial
infections.
Notably,
heparin
exhibites
stronger
inhibitory
effect
compare
similar
degrees
weights,
suggesting
particular
architectures
may
optimize
interactions.