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UCLA researchers locate and image prostate
cancer as it spreads to lymph nodes
Discovery may lead to more effective diagnostic and therapeutics
Using an engineered common
cold virus, UCLA researchers delivered a
genetic payload to prostate cancer cells
that allowed them, using Positron Emission
Tomography (PET), to locate the diseased
cells as they spread to the lymph nodes, the
first place prostate cancer goes before
invading other organs.
The tiny cancer metastases in
the pelvic lymph nodes are very difficult to
find using conventional imaging tools such
as CT scanning.
This discovery could aid
oncologists in finding the cancer's spread
earlier, when it's more treatable, and
before it invades distant organs, said Lily
Wu, a researcher at UCLA's Jonsson Cancer
Center and the senior author of the study.
The next step for Wu and her colleagues is
linking the non-invasive imaging advance
with a treatment component, activating a
toxic agent in the genetic payload to kill
the spreading cancer cells.
Wu hopes one day to be able
to find tiny prostate cancer metastases in
patients and kill them at the same time,
watching it all on a PET scanner. She
currently is refining this image-guided
therapy in her lab in mouse models.
"I think this is very exciting for many
reasons," said Wu, who also is an associate
professor of pharmacology and urology.
"We now know we can reach these prostate
cancer metastases at an earlier stage than
before, and we know we can deliver genes to
those cancer cells that produce proteins
that can be imaged by PET.
"Now we will find out how effective this
genetic toxic payload is in preventing
further spread of the cancer to other vital
organs."
The study appears July 11, 2008 in the
early, online edition of the peer-reviewed
journal Nature Medicine.
The spread of prostate cancer
to the pelvic lymph nodes is the most
reliable indicator that the patient will
have a poor prognosis, with disease
recurrence and progression likely.
Accurately assessing pelvic lymph node
involvement in patients is critical in
planning their treatment, Wu said.
Currently, physicians don't know if a
treatment is attacking cancer cells until,
using traditional imaging, they see a
decrease in tumor size, an insensitive
approach that can take weeks and months.
And if the treatment isn't working, the
patient is exposed to a toxic therapy that
isn't helping them. If Wu is successful, an
oncologist would know within days if the
cancer has spread and whether the treatment
is killing the cancer.
Using mouse models, Wu and her team
engineered a virus to travel to the lymph
nodes, using a prostate cancer-specific
vector that dictates s its protein payload
be expressed only in prostate cells.
The payload in this case is a protein that
can be imaged by PET scanning. The virus was
introduced into the tumor in the mouse and
Wu and her team were able to detect PET
signals only from the lymph nodes with
cancer cell involvement,
indicating the virus reached and infected
the prostate cancer cells and produced the
imaging protein.
As part of this study, Wu
co-developed TSTA, a two-step
transcriptional amplification method, which
increased the expression of the genetic
payload inside the cancer cells – in effect
boosting the imaging signals and potential
killing activity of the engineered virus.
Wu believes this type of image-guided
therapy has the potential to improve the way
advanced prostate cancer is treated.
"It would represent a treatment advance in
patients for whom outcome is not good," Wu
said.
"This would help improve the prognosis for
these patients by letting us find and treat
these metastases early.
"If we can catch the cancer before it
invades other organs, we have a better
chance to change the outcomes for these
patients."
This type of approach was
pioneered in the field of breast cancer with
testing of the sentinel lymph node, the
first place breast cancer goes when it
spreads.
A biopsy can determine if the cancer is in
the sentinel node, therefore spreading, and
oncologists base their treatment decisions
on that information.
In prostate cancer, the lymph nodes are much
more difficult to access for biopsy, so Wu's
method provides a much needed, non-invasive
alternative.
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