Experimental Dermatology,
Journal Year:
2023,
Volume and Issue:
32(7), P. 1063 - 1071
Published: June 7, 2023
Abstract
A
direct
contact
co‐culture
of
skin
explants
to
SZ95
sebocytes
(3D‐SeboSkin)
has
been
shown
preserve
the
integrity
epidermal
keratinocytes
and
dermis.
In
this
study,
properties
melanocytes
were
evaluated
in
same
3D
SeboSkin
ex
vivo
model.
Skin
(
n
=
6)
maintained
3D‐SeboSkin
model,
fibroblasts
alone
serum‐free
medium
(SFM).
Histopathological,
immunohistochemical,
apoptosis
oil
red
staining
evaluations
performed
at
Days
0
6
incubation.
Results
revealed
preservation
prominent
proliferation
basal
addition
dermal
collagen
vasculature
Day
culture
model
a
lesser
extent
with
but
not
SFM
alone.
Melan‐A+/Ki67‐
remained
attached
dermis
even
sites
detachment
three
explant
models
tested.
However,
number
was
significantly
conserved
cultures
comparison
p
<
0.05),
whereas
no
difference
found
fibroblasts.
Few
DAPI/TUNEL+
apoptotic
could
mostly
be
observed
SFM‐incubated
explants.
Furthermore,
only
exhibited
increased
lipogenesis
accumulation
abundant
lipid
droplets.
These
results
denote
that
yielded
significant
hence
it
is
optimal
for
studies
abnormalities
pigmentation,
melanocyte
neoplasms
effects
different
hormones,
cytokines,
carcinogens
various
therapeutics
pattern
recapitulates
environment.
Cancers,
Journal Year:
2022,
Volume and Issue:
14(11), P. 2753 - 2753
Published: June 1, 2022
(1)
Background:
There
is
a
constant
search
for
new
prognostic
factors
that
would
allow
us
to
accurately
determine
the
prognosis,
select
type
of
treatment,
and
monitor
patient
diagnosed
with
uveal
melanoma
in
minimally
invasive
easily
accessible
way.
Therefore,
we
decided
evaluate
role
its
pigmentation
clinical
assessment.
(2)
Methods:
The
154
melanomas
was
assessed
by
indirect
ophthalmoscopy.
Two
groups
tumours
were
identified:
amelanotic
pigmented.
statistical
relationships
between
these
two
clinical,
pathological
parameters
long-term
survival
rate
analyzed.
(3)
Results:
16.9%
among
all
they
occurred
younger
patients
(p
=
0.022).
In
pigmented
melanomas,
unfavourable
features
such
as:
epithelioid
cells
0.0013),
extrascleral
extension
0.027),
macronucleoli
0.0065),
absence
BAP1
expression
0.029)
statistically
more
frequently
observed.
Kaplan−Meier
analysis
demonstrated
significantly
better
overall
0.017)
disease-free
<
0.001)
rates
tumours.
However,
this
relationship
significant
lower
stage
(AJCC
II),
not
present
larger
advanced
stages
III).
(4)
Conclusions:
results
obtained
suggested
presence
ophthalmoscopy
associated
worse
compared
lesions.
These
findings
could
be
useful
choice
therapeutic
follow-up
options
future.
Cell Reports,
Journal Year:
2022,
Volume and Issue:
42(1), P. 111906 - 111906
Published: Dec. 30, 2022
Melanin
is
a
pigment
produced
from
the
amino
acid
L-tyrosine
in
melanosomes.
The
CNC-family
transcription
factor
Nrf3
expressed
basal
layer
of
epidermis,
where
melanocytes
reside,
but
its
melanogenic
function
unclear.
Here,
we
show
that
regulates
macropinocytosis
and
autophagy
to
coordinate
melanogenesis
cascade.
In
response
an
exogenous
inducer
melanin
production,
forskolin,
upregulates
core
gene
circuit,
which
includes
Mitf,
Tyr,
Tyrp1,
Pmel,
Oca2.
Furthermore,
induces
expression
Cln3,
autophagosome-related
factor,
for
precursor
uptake
by
macropinocytosis.
Ulk2
Gabarapl2
are
also
identified
as
Nrf3-target
genes
melanosome
formation.
parallel,
prompts
autolysosomal
degradation
melanocyte
survival.
An
endogenous
αMSH
activates
Nrf3-mediated
whereas
it
suppressed
HIV-1
protease
inhibitor,
nelfinavir.
These
findings
indicate
significant
role
anti-melanogenic
potential
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(16), P. 12809 - 12809
Published: Aug. 15, 2023
The
visual
appearance
of
humans
is
derived
significantly
from
our
skin
and
hair
color.
While
melanin
epidermal
melanocytes
protects
the
damaging
effects
ultraviolet
radiation,
biological
value
pigmentation
in
follicle,
particularly
on
scalp,
less
clear.
In
this
study,
we
explore
heterogeneity
pigment
cells
human
scalp
anagen
follicle
bulb,
a
site
conventionally
viewed
to
be
focused
solely
production
for
transfer
shaft.
Using
c-KIT/CD117
microbeads,
isolated
bulbar
c-KIT-positive
c-KIT-negative
melanocytes.
both
subpopulations
expressed
MITF,
only
fraction
SOX10.
We
further
localized
melanocyte
(expressing
c-KIT,
SOX10,
DCT)
that
exhibited
distinct/variable
expression
downstream
differentiation-associated
melanosome
markers
(e.g.,
gp100
Melan-A).
localization
second
‘immature’
SOX10
negative
population,
which
was
c-KIT/MITF
double-positive,
identified
outside
melanogenic
zone
most
peripheral/proximal
matrix.
This
study
describes
an
approach
purifying
bulb
melanocytes,
allowing
us
identify
unexpected
levels
heterogeneity.
function
more
immature
part
remains
elucidated.
Could
they
in-transit
migratory
ultimately
destined
synthesize
melanin,
or
could
contribute
non-melanogenic
ways?
Cancers,
Journal Year:
2024,
Volume and Issue:
16(8), P. 1461 - 1461
Published: April 11, 2024
Melanoma
ranks
as
the
fifth
most
common
solid
cancer
in
adults
worldwide
and
is
responsible
for
a
significant
proportion
of
skin-tumor-related
deaths.
The
advent
immune
checkpoint
inhibition
with
anti-programmed
death
protein-1
(PD-1)
antibodies
has
revolutionized
adjuvant
treatment
high-risk,
completely
resected
stage
III/IV
melanoma.
However,
not
all
patients
benefit
equally.
Current
strategies
improving
outcomes
involve
earlier
disease
stages
(IIB/C)
well
perioperative
approaches.
Interfering
T-cell
exhaustion
to
counteract
evasion
immunogenic
nature
melanoma
key
anti-PD-1
effectiveness.
Yet,
biological
rationale
efficacy
clinically
tumor-free
remains
be
fully
elucidated.
High-dose
intermittent
sun
exposure
(sunburn)
well-known
primary
risk
factor
melanomagenesis.
Also,
ultraviolet
radiation
(UVR)-induced
immunosuppression
may
impair
anti-cancer
surveillance.
In
this
review,
we
summarize
current
knowledge
about
blockade,
including
characterization
main
cell
types
likely
its
efficacy.
conclusion,
propose
that
local
systemic
immunosuppression,
some
extent
UVR-mediated,
can
restored
by
therapy,
consequently
boosting
anti-melanoma
surveillance
elimination
residual
clones.
The
visual
appearance
of
humans
derives
significantly
from
our
skin
and
hair
color.
While
melanin
epidermal
melanocytes
protects
the
damaging
effects
ultraviolet
radiation,
biological
value
pigmentation
in
follicle,
particularly
scalp,
is
less
clear.
In
this
study,
we
explore
heterogeneity
pigment
cells
human
scalp
anagen
follicle
bulb,
a
site
conventionally
viewed
to
be
focused
solely
on
production
for
transfer
shaft.
Using
c-KIT/CD117
microbeads,
isolated
bulbar
c-KIT-positive
c-KIT-negative
melanocytes.
both
subpopulations
expressed
MITF,
only
fraction
SOX10.
We
further
localized
melanocyte
(expressing
c-KIT,
SOX10,
DCT)
that
exhibited
distinct/variable
expression
downstream
differentiation-associated
melanosome
markers
(e.g.,
gp100
Melan-A).
Localization
second
‘immature’
SOX10
negative
population,
which
was
c-KIT/MITF
double
positive,
identified
outside
melanogenic
zone
most
peripheral/proximal
matrix.
These
studies
describe
an
approach
purifying
bulb
melanocytes,
allowing
us
identify
unexpected
levels
heterogeneity.
function
more
immature
part
remains
elucidated.
Could
they
in-transit
migratory
destined
synthesize
mela-nin
ultimately
or
could
contribute
non-melanogenic
ways.
BioEssays,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 4, 2024
Abstract
Melanomas
arise
from
transformed
melanocytes,
positioned
at
the
dermal‐epidermal
junction
in
basal
layer
of
epidermis.
Melanocytes
are
completely
surrounded
by
keratinocyte
neighbors,
with
which
they
communicate
through
direct
contact
and
paracrine
signaling
to
maintain
normal
growth
control
homeostasis.
UV
radiation
sunlight
reshapes
this
communication
network
drive
a
protective
tanning
response.
However,
repeated
rounds
sun
exposure
result
accumulation
mutations
melanocytes
that
have
been
considered
as
primary
drivers
melanoma
initiation
progression.
It
is
now
clear
not
sufficient
tumor
formation—the
environment
plays
critical
role.
This
review
focuses
on
changes
melanocyte‐keratinocyte
contribute
progression,
particular
focus
recent
mechanistic
insights
lay
foundation
for
developing
new
ways
intercept
development.