Specially designed
nanoparticles can
reveal tiny
cancerous tumors
that are invisible
by ordinary means of
detection, according
to a study by
researchers at
Washington
University School of
Medicine in St.
Louis.
The researchers
demonstrated that
very small human
melanoma tumors
growing in
mice—indiscernible
from the surrounding
tissue by direct MRI
scan—could be easily
located as soon as
30 minutes after the
mice were injected
with MRI contrast
agent attached to
the nanoparticles.
Because
nanoparticles can be
engineered to carry
a variety of
substances, they
also may be able to
deliver
cancer-fighting
drugs to malignant
tumors as
effectively as they
carry the imaging
materials that
spotlight cancerous
growth.
"One of the best
advantages of the
particles is that we
designed them to
detect tumors using
the same MRI
equipment that is in
standard use for
heart or brain
scans," says senior
author Gregory Lanza,
MD, PhD, associate
professor of
medicine. "We
believe the
technology is very
close to being
useful in a hospital
setting."
Nanoparticles are
particularly useful
because of their
adaptability,
according to Lanza,
who sees patients at
Barnes Jewish
Hospital. "We can
also make these
particles so that
they can be seen
with nuclear
imaging, CT scanning
and ultrasound
imaging," Lanza
says.
Lanza and his
colleague Samuel
Wickline, MD,
professor of
medicine, are
co-inventors of this
nanoparticle
technology. The
effectiveness of the
nanoparticles in
diagnosis and
therapy in humans
will be tested in
clinical trials in
about 18 months to
two years.
In this study,
MRI scans picked up
tumors that were
only a couple of
millimeters wide.
Small, rapidly
growing tumors cause
growth of new blood
vessels, which feed
the tumors. To get
the particles to
bind to tumors, the
researchers equipped
them with tiny
"hooks" that link
only to
complementary
"loops" found on
cells in newly
forming blood
vessels. When the
nanoparticles hooked
the "loops" on the
new vessels' cells,
they revealed the
location of the
tumors.
The particles can
be loaded with a
wide variety of
drugs that will then
be directed to
growing tumors.
"When drug-bearing
nanoparticles also
contain an imaging
agent, you can get a
visible signal that
allows you to
measure how much
medication got to
the tumor," Lanza
says. "You would
know the same day
you treated the
patient and if the
drug was at a
therapeutic level."
Using
nanoparticles, drug
doses could be much
smaller than doses
typically used in
chemotherapy, making
the procedure
potentially much
safer.
"The other side
of that is you have
the ability to focus
more drug at the
tumor site, so the
dose at the site
might be ten to a
thousand times
higher than if you
had administered the
drug systemically,"
Lanza says.
The nanoparticles
also may permit more
effective follow up,
because a doctor
could use them to
discern whether a
tumor was still
growing after
radiation or
chemotherapy
treatments.
Although this
study focused on
melanoma tumors, the
researchers believe
the technology
should work for most
solid tumors,
because all tumors
must recruit new
blood vessels to
obtain nutrients as
they grow.
Nevertheless,
melanoma has unique
traits that make it
especially
interesting as a
target for
nanoparticle
therapy. Melanoma
has a horizontal
phase, when it
spreads across the
skin surface, and a
vertical phase, when
it goes deep into
the body and grows
quickly.
"Once melanoma
has moved into its
vertical phase, it
is almost
untreatable because
by the time the
tumors are large
enough to detect,
it's too late,"
Lanza says. "With
the nanoparticles,
we believe we would
be able to see the
smallest melanoma
tumors when they are
just large enough to
begin new blood
vessel formation.
Plus, we should be
able to deliver
chemotherapeutic
drugs right to
melanoma cells,
because melanoma
tumors create blood
vessels using their
own cells."
Source:
Washington
University School of
Medicine.