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Good Day My FRiends Thought this might be of some interest. file:///C|/windows/temp/nscomm40/tmp/tmp4/edt1.htm God Bless You, marty auslanderTitle: Internet Home - American Association for Cancer Research (AACR) NEW DELIVERY SYSTEM FOR TUMOR-SUPPRESSOR GENE P53 HOLDS
Research results presented at International Conference sponsored
jointly by AACR,
NCI and EORTC
Washington, DC … November 18, 1999 --- Researchers announced today
that they
developed a new system to deliver the tumor-suppressor gene p53
directly into the tumor
through the bloodstream, which, when used in combination with
radiotherapy and
chemotherapy, may significantly improve treatment outcomes for
prostate cancer patients.
Results were presented today at the International Conference
on Molecular Cancer
Therapeutics - Discovery, Development and Clinical Validation
sponsored by the
American Association for Cancer Research (AACR), the National
Cancer Institute
(NCI), and the European Organization for Research and Treatment
of Cancer (EORTC).
"Our data demonstrate that by introducing p53 in this new way,
we can sensitize prostate
tumors to radiation and chemotherapeutic agents. Also, by delivering
the p53 gene
directly into the bloodstream, we can increase the number of
cancer cells that are targeted
and reached - the cells of the actual tumor and those that may
be roaming throughout the
body," says Kathleen F. Pirollo, Ph.D., research associate professor
at the Lombardi
Cancer Center at Georgetown University in Washington, DC.
Abnormalities in p53 have been found in the majority of human
cancers. This gene is
influential in causing programmed cell death, called apoptosis,
and has been the focus of
several studies attempting to introduce "normal" copies of this
gene into cancer cells in
order to stop the disease. The most common way of introducing
the normal p53 gene into
cancer cells has been to carry it through a modified common cold
virus, the adenovirus.
However, limitations to this method have occurred in terms of
the number of cells
reached, the ability to target only the cancer cells, and possible
adverse effects.
The new delivery system uses a combination of three compounds
-- ligands, p53 and
liposomes -- in a carefully developed ratio to produce a small
enough structure to
penetrate into the small blood vessels in the tumor. Ligands
are molecules that recognize
and attach to specific protein sequences or receptors on the
surface of cells with high
specificity, meaning that they recognize and attach only to tumor
cells. Tumor cells have
many more of these than most normal cells. Folic acid or transferrin
(the protein that
carries iron in the bloodstream) are used as the ligands since
they are highly recognized
by tumors and can attach easily to tumor cells. Liposomes are
fatty particles that enclose
and protect the p53 gene DNA. The p53 gene is enclosed in the
liposome, which in turn
is attached to the ligand, and the combined entity is released
into the blood to find its way
to the cancer cells. When the normal p53 is reintroduced into
the cancer cells, these cells
become more sensitive to common chemotherapy drug and radiation
therapy, thus killing
more of the tumor.
The AACR is the oldest and largest scientific organization in
the world focused on the
multidisciplinary aspects of basic, clinical, and translational
cancer research for the
prevention and cure of cancer. Its 15,000 members come from 80
countries. The NCI is
part of the National Institutes of Health. The EORTC is an international
research
organization whose goal is to facilitate the transition from
experimental discovery into
state-of-the-art treatment of cancer. The NCI-EORTC Symposium
on New Drugs in
Cancer Therapy has been held biennially in Amsterdam for two
decades. Under the
auspices of these three prestigious organizations, it will now
occur annually to help
researchers keep up with the rapid pace of discovery in molecular
biology and genetics
that is identifying new targets for cancer therapeutics.
###
"Ligand-targeted, liposome-mediate p53 gene therapy in combination
with
radiation or chemotherapy leads to prostate tumor regression"
(abstract #508)
Kathleen F. Pirollo, Ph.D., Lombardi Cancer Center/Georgetown
University
Poster Session 5, Section 2, Board 16 - Exhibit Hall
Thursday, November 18 -- 12:15 pm - 2:15 pm
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