Evaluating TcAs for Use in Biotechnology Applications
Cole L. Martin,
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John H. Hill,
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Brian D. Wright
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et al.
BioTech,
Journal Year:
2025,
Volume and Issue:
14(1), P. 5 - 5
Published: Jan. 25, 2025
ABC
toxin
complexes
(Tcs)
are
tripartite
that
come
together
to
form
nano-syringe-like
translocation
systems.
Tcs
often
compared
with
Bacillus
thuringiensis
(Bt)
toxins,
and
as
such,
they
have
been
highly
studied
a
potential
novel
pesticide
combat
growing
insect
resistance.
Moreover,
it
is
possible
substitute
the
cytotoxic
hypervariable
region
alternative
peptides,
which
promise
use
peptide
delivery
system.
These
toxins
possess
unique
ability
active
chimeric
holotoxins
across
species
display
capability
translocate
variety
of
payloads
membrane
bilayers.
Additionally,
mutagenesis
on
linker
receptor
binding
domains
(RBDs)
show
mutations
do
not
inherently
cause
loss
functionality
for
translocation.
For
these
reasons,
emerged
an
ideal
candidate
targeted
protein
engineering.
However,
elucidation
specific
function
each
RBD
in
relation
target
recognition
currently
limits
rational
design
approach
any
Tc.
there
distinct
lack
targeting
biodistribution
data
many
among
mammals
mammalian
cell
lines.
Here,
we
outline
two
separate
strategies
modifying
capabilities
A
subunit
(TcA)
from
Xenorhabdus
nematophilus,
Xn-XptA2.
We
identify
structural
differences
make
Xn-XptA2
different
than
other
characterized
TcAs
modular
substituting
RBDs
into
scaffold.
Finally,
first,
our
knowledge,
TcA
mice.
Language: Английский
Research progress on cholesterol metabolism and tumor therapy
Discover Oncology,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: April 30, 2025
Cholesterol
and
its
metabolic
derivatives
have
important
biological
functions
are
crucial
in
tumor
initiation,
progression,
treatment.
maintains
the
physical
properties
of
cellular
membranes
is
pivotal
cell
signal
transduction.
metabolism
includes
both
de
novo
synthesis
uptake
from
extracellular
sources
such
as
low-density
lipoprotein
(LDL)
high-density
(HDL).
This
review
explores
aspects
to
provide
a
comprehensive
understanding
their
roles
cancer.
involved
bile
acid
production
steroid
hormone
biosynthesis
closely
linked
reprogramming
endogenous
exogenous
signals
within
microenvironment.
These
intricately
associated
with
key
processes
proliferation,
survival,
invasion,
metastasis.
Evidence
suggests
that
regulating
cholesterol
may
offer
therapeutic
benefits
by
inhibiting
growth,
remodeling
immune
microenvironment,
enhancing
antitumor
responses.
summarizes
role
biology
discusses
application
statins
other
inhibitors
cancer
therapy,
aiming
novel
insights
for
development
drugs
targeting
advances
diagnosis
Language: Английский
Mobocertinib antagonizes multidrug resistance in ABCB1- and ABCG2-overexpressing cancer cells: in vitro and in vivo studies
Xing-Duo Dong,
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Meng Zhang,
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Qiu‐Xu Teng
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et al.
Cancer Letters,
Journal Year:
2024,
Volume and Issue:
unknown, P. 217309 - 217309
Published: Oct. 1, 2024
Language: Английский
Ketogenesis promotes triple-negative breast cancer metastasis via calpastatin β-hydroxybutyrylation
Haoran Jiang,
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Yuan Zeng,
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Xiaoye Yuan
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et al.
Lipids in Health and Disease,
Journal Year:
2024,
Volume and Issue:
23(1)
Published: Nov. 12, 2024
Triple-negative
breast
cancer
(TNBC)
continues
to
pose
a
significant
obstacle
in
the
field
of
oncology.
Dysregulation
lipid
metabolism,
notably
upregulated
ketogenesis,
has
emerged
as
hallmark
TNBC,
yet
its
role
metastasis
been
elusive.
Here,
by
utilizing
clinical
specimens
and
experimental
models,
study
demonstrates
that
increased
ketogenesis
fosters
TNBC
promoting
up-regulation
β-hydroxybutyrate
(β-OHB),
key
ketone
body.
Mechanistically,
β-OHB
facilitates
β-hydroxybutyrylation
(Kbhb)
Calpastatin
(CAST),
an
endogenous
calpain
(CAPN)
inhibitor,
at
K43,
blocking
interaction
with
CAPN
subsequently
FAK
phosphorylation
epithelial‒mesenchymal
transition
(EMT).
In
conclusion,
reveals
novel
regulatory
axis
linking
metastasis,
shedding
light
on
intricate
interplay
between
metabolic
reprogramming
tumor
progression.
Language: Английский
DNA Repair Status as a Guide for Pancreatic Ductal Adenocarcinoma Treatment, an Old View for a New Future.
Cancer Letters,
Journal Year:
2024,
Volume and Issue:
604, P. 217222 - 217222
Published: Sept. 7, 2024
Language: Английский
The BET inhibitor sensitivity is associated with the expression level of CDC25B in pancreatic cancer models
Aubrey L. Miller,
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Patrick L. Garcia,
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Rebecca B. Vance
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et al.
Cancer Drug Resistance,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 18, 2024
Cell
division
cycle
25B
(CDC25B)
belongs
to
the
CDC25
family
of
phosphatases
that
regulate
cell
progression.
CDC25B
also
contributes
tumor
initiation
and
progression,
but
no
connection
between
levels
drug
sensitivity
in
pancreatic
cancer
has
been
reported.
Based
on
our
finding
bromodomain
extraterminal
domain
(BET)
inhibitors
decrease
CDC25B,
we
aim
compare
models
expressing
contrasting
BET
inhibitor
JQ1,
lines
Language: Английский