Journal of Breast Cancer,
Год журнала:
2018,
Номер
21(3), С. 233 - 233
Опубликована: Янв. 1, 2018
Breast
cancer
has
the
highest
incidence
among
all
malignancies
diagnosed
in
women.
Therapies
have
significantly
improved
over
years
due
to
extensive
molecular
and
clinical
research;
a
large
number
of
cases,
targeted
therapies
provided
better
prognosis.
However,
one
specific
subtype
remains
elusive
therapies-the
triple-negative
breast
cancer.
This
immunohistochemically
defined
is
resistant
both
endocrine
therapies,
leading
its
poor
A
field
that
great
promise
current
research
epigenetics.
By
studying
epigenetic
mechanisms
underlying
tumorigenesis-DNA
methylation,
histone
modifications,
noncoding
RNAs-advances
treatment,
diagnosis,
prevention
are
possible.
review
aims
synthesize
discoveries
been
made
related
Clinical Genitourinary Cancer,
Год журнала:
2023,
Номер
21(5), С. 537 - 545
Опубликована: Июнь 23, 2023
Kidney
renal
papillary
cell
carcinoma
(KIRP)
is
a
common
type
of
carcinoma.
DNA
methylation
plays
an
important
role
in
the
development
several
cancers.
The
aim
our
study
was
to
identify
differentially
expressed
genes
associated
with
abnormal
as
biomarkers
for
predicting
outcome
KIRP.We
downloaded
KIRP
data,
RNA
sequencing
(RNAseq)
and
their
corresponding
clinical
information
from
Cancer
Genome
Atlas
(TCGA)
database.
ChAMP
DEGseq2
packages
R
software
were
used
screen
methylated
probes
(DMPs)
(DEGs).
Univariate
multivariate
Cox
regression
analyses
suitable
immune
related
correlated
aberrant
methylations
prognosis
biomarkers.We
identified
8
DEGs
(Cysteine
And
Glycine
Rich
Protein
1
[CSRP1],
major
histocompatibility
complex,
Class
II,
DM
Beta
[HLA-DMB],
LIF
Receptor
Subunit
Alpha
[LIFR],
Leukotriene
B4
receptor
2
[LTB4R2],
Mitogen-Activated
Kinase
14
[MAP3K14],
Nuclear
Subfamily
Group
F
Member
[NR2F1],
Secreted
Transmembrane
[SECTM1],
Vimentin
[VIM])
that
independently
overall
survival
(months)
(OS)
KIRP.
time
dependent
area
under
curve
(AUC)
each
receiver
operating
characteristic
(ROC)
risk
assessment
model
at
1,
3,
5,
10-years
reached
0.8415,
0.8131,
0.7873,
0.7667.
cells
factors.
AUC
value
diagnosis
using
those
0.99.The
constructed
by
well
able
predict
diagnose
However,
whether
could
be
applied
practice
requires
further
study.
Human Reproduction Update,
Год журнала:
2019,
Номер
26(3), С. 423 - 449
Опубликована: Ноя. 21, 2019
Abstract
BACKGROUND
Endometriosis
is
a
benign
gynaecological
disease.
Thus,
it
came
as
complete
surprise
when
was
reported
recently
that
the
majority
of
deep
endometriosis
lesions
harbour
somatic
mutations
and
sizeable
portion
them
contain
known
cancer-associated
(CAMs).
Four
more
studies
have
since
been
published,
all
demonstrating
existence
CAMs
in
different
subtypes
endometriosis.
While
field
still
evolving,
confirmation
has
raised
many
questions
were
previously
overlooked.
OBJECTIVE
AND
RATIONALE
A
comprehensive
overview
produced.
In
addition,
with
emerged
understanding
natural
history
endometriotic
well
normal
apparently
healthy
tissues,
this
review
attempts
to
address
following
questions:
Why
there
such
wild
discrepancy
mutation
frequencies?
does
ectopic
endometrium
higher
rate
than
eutopic
endometrium?
Would
presence
increase
risk
cancer
bearers?
do
epithelial
cells
much
frequencies
their
stromal
counterpart?
What
clinical
implications,
if
any,
for
Do
these
tell
us
anything
about
pathogenesis
and/or
pathophysiology
endometriosis?
SEARCH
METHODS
The
PubMed
database
searched,
from
its
inception
September
2019,
papers
English
using
term
‘endometriosis
CAM’,
cancer-driver
mutation’,
‘somatic
mutations’,
‘fibrosis’,
‘fibrosis
epigenetic’,
‘CAMs
tumorigenesis’,
tissues’,
‘oestrogen
receptor
fibrosis’,
‘oxidative
stress
‘ARID1A
‘Kirsten
rat
sarcoma
therapeutics’.
All
retrieved
read
and,
relevant,
incorporated
into
results.
OUTCOMES
Seven
identified
various
sequencing
methods
retrieved,
results
somewhat
different.
Yet,
apparent
those
microdissection
techniques
accurate
found
CAMs,
echoing
recent
discoveries
tissues
also
result
replicative
aging
process.
Hence
lesions,
irrespective
subtype,
left
intact,
would
generate
part
aging,
oxidative
perhaps
other
factors
yet
be
some
rare
cases,
develop
cancer.
published
data
are
unable
paint
clear
picture
on
However,
turnover
counterpart
due
cyclic
bleeding,
component
can
formed
by
refresh
influx
mesenchymal
through
epithelial–mesenchymal
transition,
endothelial–mesenchymal
mesothelial–mesenchymal
transition
processes
recruitment
bone-marrow-derived
stem
outflow
smooth
muscle
metaplasia,
counterpart.
cellular
components
dependent
co-evolving
manner.
Genes
involved
likely
active
players
lesional
fibrogenesis,
hyperestrogenism
drivers
both
fibrogenesis.
Finally,
harbouring
conceivably
refractory
medical
treatment,
due,
no
small
part,
high
fibrotic
content
reduced
vascularity
cellularity.
WIDER
IMPLICATIONS
accumulating
shed
new
light
They
suggest
challenges
management.
distinct
developmental
trajectories
stroma
epithelium
underscore
importance
microenvironment
ever-changing
identity.
Mutational
profiling
women
ages
reproductive
needed
order
gain
deeper
pathogenesis.
Moreover,
one
area
conspicuously
received
scant
attention
epigenetic
landscape
ectopic,
endometrium.
Journal of Breast Cancer,
Год журнала:
2018,
Номер
21(3), С. 233 - 233
Опубликована: Янв. 1, 2018
Breast
cancer
has
the
highest
incidence
among
all
malignancies
diagnosed
in
women.
Therapies
have
significantly
improved
over
years
due
to
extensive
molecular
and
clinical
research;
a
large
number
of
cases,
targeted
therapies
provided
better
prognosis.
However,
one
specific
subtype
remains
elusive
therapies-the
triple-negative
breast
cancer.
This
immunohistochemically
defined
is
resistant
both
endocrine
therapies,
leading
its
poor
A
field
that
great
promise
current
research
epigenetics.
By
studying
epigenetic
mechanisms
underlying
tumorigenesis-DNA
methylation,
histone
modifications,
noncoding
RNAs-advances
treatment,
diagnosis,
prevention
are
possible.
review
aims
synthesize
discoveries
been
made
related