Washington D.C [USA], Oct.23 (ANI): A new finding has suggested that rare variants combined with background genetic risk factors may account for many unexplained cases of familial breast cancer.
The study further states that knowing the specific genes involved could inform choice of prevention and treatment strategies.
Researcher Na Li, who presented the work, and lead investigator Ian Campbell and his team from the Peter MacCallum Cancer Centre in Melbourne, Australia, emphasized that their study was conducted on patients with a high risk of breast cancer, especially those with a personal or family history and were seeking an explanation.
"When you know which gene is conferring the risk of breast cancer, you can provide a more precise estimate of the risk, know what to expect and watch out for, and (offer) tailor risk management strategies to the patient," said Dr. Campbell.
Unfortunately, in about half of these high-risk patients, no known genetic cause was found, suggesting a more complicated explanation. In such cases, cancer geneticists have long suspected that polygenic risk (risk conferred by a combination of genetic variants) was involved.
Dr. Li also explained that genes do not work on their own, but rather as part of one's overall genetic context.
"That 'polygenic risk' background is like a landscape full of hills and valleys, with each risky variant like a house on top of it," she said.
"If you inherit a high-risk variant -- a tall house -- but live in a valley, your overall risk of breast cancer may end up being average because your genetic landscape pulls it down," he told.
Even though the concept of background genetic risk is not new as for many years the scientists did not have the tools to collect and analyze the thousands of genomes needed to quantify it.
However, recent improvements in next-generation sequencing technology have addressed this challenge. Therefore, as a result, Dr. Li and colleagues were able to sequence up to 1,400 candidate breast cancer genes in 6,000 familial breast cancer patients and 6,000 cancer-free controls.
In this large sample, they searched for potential cancer-associated genes suggested by the literature, collaborators, and their own previous results, and identified at least 46 genes that were at least twice as likely to have mutations among participants with breast cancer as in those without.
The researcher also used the data to calculate a polygenic risk score for each patient, and combined this score with data on their high and moderate-risk variants to estimate each patient's overall risk of developing breast cancer.
In the coming years, the researchers plan to expand the study internationally to further test and refine their findings across populations. They also hope to bring these more precise risk estimates into the clinic, to more accurately reassure women about their personal risk of cancer, or -- if risk is high -- advise preventive strategies such as screening at a younger age.
The study appears in the journal of American Society of Human Genetics. (ANI)