Clinical & Translational Oncology,
Год журнала:
2024,
Номер
26(4), С. 1022 - 1032
Опубликована: Янв. 4, 2024
Abstract
Background
Cellular
senescence
is
a
state
characterized
by
cell-cycle
arrest
and
apoptotic
resistance.
Senescence
in
cancer
may
be
induced
oncogenes
or
therapy.
While
cellular
might
play
an
important
role
protection
against
development,
elevated
uncontrolled
senescent
cells
accumulation
promote
carcinogenesis
secreting
collection
of
pro-inflammatory
factors,
collectively
termed
the
senescence-associated
secretory
phenotype
(SASP).
Material
methods
We
determined
gene
expression
at
mRNA
level
selected
markers
(p16
LMNB1)
SASP
factors
(IL-6,
IL-1b,
CXCL-1
TNF-α)
72
cancerous
tissues
64
normal
obtained
from
patients
with
head
neck
squamous
cell
carcinoma
(HNSCC)
correlated
this
data
patients’
clinical
follow-up.
Results
Our
results
indicate
higher
levels
compared
to
tissues.
presented
relationship
between
transcript
progression
disease.
Moreover,
we
proposed
CXCL1
as
candidate
biomarker
differentiating
ones
IL1b
molecular
factor
related
increased
TNM
stage.
Conclusion
primary
study
indicates
that
associated
some
clinicopathological
features.
However,
more
detailed
needed
present
specific
senescence-related
mechanism
SASPs
especially
tumor
therapy
response
relation
patient’s
immune
system
condition.
Cancer Cell International,
Год журнала:
2025,
Номер
25(1)
Опубликована: Март 26, 2025
Abstract
Multiple
myeloma
(MM)
is
a
hematological
malignancy
defined
by
the
abnormal
proliferation
and
accumulation
of
plasma
cells
(PC)
within
bone
marrow
(BM).
While
multiple
impacts
bone,
it
not
classified
as
primary
cancer.
The
microenvironment
significantly
influences
progression
its
treatment
response.
Mesenchymal
stromal
(MSCs)
in
this
environment
engage
with
other
components
via
direct
contact
secretion
soluble
factors.
This
review
examines
established
roles
MSCs
facets
MM
pathology,
encompassing
their
pro-inflammatory
functions,
contributions
to
tumor
epigenetics,
effects
on
immune
checkpoint
inhibitors
(ICIs),
influence
reprogramming,
chemotherapy
resistance,
senescence.
investigates
role
development
MM.
Cancers,
Год журнала:
2022,
Номер
14(8), С. 1963 - 1963
Опубликована: Апрель 13, 2022
Long
non-coding
RNAs
(lncRNAs)
are
transcripts
longer
than
200
nucleotides
that
not
translated
into
proteins.
Nowadays,
lncRNAs
gaining
importance
as
key
regulators
of
gene
expression
and,
consequently,
several
biological
functions
in
physiological
and
pathological
conditions,
including
cancer.
Here,
we
point
out
the
role
pathogenesis
multiple
myeloma
(MM).
We
focus
on
their
ability
to
regulate
processes
identified
“hallmarks
cancer”
enable
malignant
cell
transformation,
early
tumor
onset
progression.
The
aberrant
MM
suggests
potential
use
clinical
biomarkers
for
diagnosis,
patient
stratification,
management.
Moreover,
they
represent
ideal
candidates
therapeutic
targeting.
Cells,
Год журнала:
2023,
Номер
12(8), С. 1209 - 1209
Опубликована: Апрель 21, 2023
DNA
repair
(DNA
damage)
foci
observed
24
h
and
later
after
irradiation
are
called
“residual”
in
the
literature.
They
believed
to
be
sites
for
complex,
potentially
lethal
double
strand
breaks.
However,
features
of
their
post-radiation
dose-dependent
quantitative
changes
role
processes
cell
death
senescence
still
insufficiently
studied.
For
first
time
one
work,
a
simultaneous
study
association
number
residual
key
damage
response
(DDR)
proteins
(γH2AX,
pATM,
53BP1,
p-p53),
proportion
caspase-3
positive,
LC-3
II
autophagic
SA-β-gal
senescent
cells
was
carried
out
24–72
fibroblast
with
X-rays
at
doses
1–10
Gy.
It
shown
that
an
increase
from
72
h,
positive
decrease,
while
cells,
on
contrary,
increases.
The
highest
noted
48
irradiation.
In
general,
results
obtained
provide
important
information
understanding
dynamics
development
cellular
populations
irradiated
fibroblasts.
Clinical & Translational Oncology,
Год журнала:
2024,
Номер
26(4), С. 1022 - 1032
Опубликована: Янв. 4, 2024
Abstract
Background
Cellular
senescence
is
a
state
characterized
by
cell-cycle
arrest
and
apoptotic
resistance.
Senescence
in
cancer
may
be
induced
oncogenes
or
therapy.
While
cellular
might
play
an
important
role
protection
against
development,
elevated
uncontrolled
senescent
cells
accumulation
promote
carcinogenesis
secreting
collection
of
pro-inflammatory
factors,
collectively
termed
the
senescence-associated
secretory
phenotype
(SASP).
Material
methods
We
determined
gene
expression
at
mRNA
level
selected
markers
(p16
LMNB1)
SASP
factors
(IL-6,
IL-1b,
CXCL-1
TNF-α)
72
cancerous
tissues
64
normal
obtained
from
patients
with
head
neck
squamous
cell
carcinoma
(HNSCC)
correlated
this
data
patients’
clinical
follow-up.
Results
Our
results
indicate
higher
levels
compared
to
tissues.
presented
relationship
between
transcript
progression
disease.
Moreover,
we
proposed
CXCL1
as
candidate
biomarker
differentiating
ones
IL1b
molecular
factor
related
increased
TNM
stage.
Conclusion
primary
study
indicates
that
associated
some
clinicopathological
features.
However,
more
detailed
needed
present
specific
senescence-related
mechanism
SASPs
especially
tumor
therapy
response
relation
patient’s
immune
system
condition.