Genetic test could predict breast cancer years in advance

Experts say a genetic test could help predict breast cancer many years before the disease is diagnosed.

Ultimately the findings, in the journal Cancer Research, could lead to a simple blood test to screen women, they say.

The test looks for how genes are altered by environmental factors like alcohol and hormones – a process known as epigenetics.

One in five women is thought to have such a genetic “switch” that doubles breast cancer risk.

The scientists from Imperial College London analyzed blood samples from 1,380 women of various ages, 640 of whom went on to develop breast cancer.

And they found a strong link between breast cancer risk and molecular modification of a single gene called ATM, which is found on white blood cells.

They then looked for evidence of what was causing this change. Specifically, they looked for a chemical effect called methylation, which is known to act as a “gene switch”.

Women showing the highest methylation levels affecting the ATM gene were twice as likely to develop breast cancer compared with those with the lowest levels.

In some cases the changes were evident up to 11 years before a breast tumor was diagnosed.

Dr. James Flanagan, of Imperial College London, who led the new research, said: “We know that genetic variation contributes to a person’s risk of disease.

“With this new study we can now also say that epigenetic variation, or differences in how genes are modified, also has a role.

“We hope that this research is just the beginning of our understanding about the epigenetic component of breast cancer risk and in the coming years we hope to find many more examples of genes that contribute to a person’s risk.

“The challenge will be how to incorporate all of this new information into the computer models that are currently used for individual risk prediction.”

It is not yet clear why breast cancer risk might be linked to changes in a white blood cell gene.

But the team envisages that a blood test could be used in combination with other information about breast cancer risk, such as family history and the presence of other known breast cancer genes, to help identify those women at greatest risk of developing the disease in the future.

These women could then be closely monitored and offered pre-emptive treatment, such as surgery.