The presence of genetic changes in the germ line that predispose to
cancer, and the development of molecular diagnostic techniques that
identify these changes, will make it possible to identify individuals in
the population who are at higher risk of developing cancer. The
identification of such individuals introduces the possibility of
intervention to prevent the development of cancer or, if cancer does
occur, to prevent it from causing death. The obvious scientific importance
of this field, as well as the likely public demand for testing, identifies
this area as a major target for investigation and development. However,
before the scientific advances that make it possible to identify
individuals predisposed to develop cancer can be translated into improved
health for these individuals, a number of major scientific, clinical,
epidemiological, ethical, and psycho-social questions must be answered.
The long term goal of the work proposed in this application is to create
a registry of families based on the population of the province of Ontario
using rigorously defined methods of sampling. This registry will allow us
to participate in collaborative research that will lead to an improved
understanding of the contributions made to the etiology of breast cancer
by environmental and genetic factors, to identify the factors responsible,
and to gain an understanding of how they act, both separately and
together, to influence risk of breast cancer. This information will be
exploited in research into methods of preventing the disease.
The specific goals of this proposal are:
l. To collect pedigree information, epidemiologic data and related
biological specimens from family members selected from the population of
Ontario. We propose to meet this objective by using existing resources to
assemble a population based series of family members at increased risk of
breast cancer and a sample of members of families in which sporadic breast
cancer has occurred to act as a non-familial comparison group for
epidemiologic and other studies.
2. To identify a population at high risk for breast cancer that will
participate in the evaluation of new preventive and therapeutic
strategies. This population will be identified from the high risk families
included in the registry as well as family members identified through the
participating cancer centers and clinics.
Error Notice
The database may currently be offline for maintenance and should be operational soon. If not, we have been notified of this error and will be reviewing it shortly.
We apologize for the inconvenience.
- The DCCPS Team.