Gene mutations should be tested routinely for ovarian cancer, say scientists

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Scientists from The University of Manchester have shown that testing for two gene families linked to a lifetime epithelial ovarian cancer risk of between 5% and 20% has a much higher than expected detection rate.

Routine testing for mutations in (HR) and (MMR) genes in women with the disease who also have a family history of ovarian, breast and other cancers, would save lives, they say.

The study, published in the journal Genetics in Medicine, is the largest study of cancer causing in to date. The research team tested 277 women with ovarian cancer whose close relatives had been diagnosed with the disease over their lifetime. Of those who tested negative for BRCA1 and 2 gene mutations, 22% were positive for HR and MMR, twice as high as the equivalent detection rate in .

Currently, doctors routinely test for cancer causing BRCA1 and BRCA2 genes which are associated with a lifetime risk of 20% to 60% and 10% to 25% respectively. However, though they do test for the other genes—it is not routine.

HR genes work in combination with BRCA genes and MMR genes are associated with Lynch syndrome, a condition passed from parents to children which increases the risk of different cancers. One of the HR genes—known as BRIP1—was the responsible for most cancers after BRCA1 and BRCA2.

Identifying the mutations in people with advanced cancer could allow doctors to prescribe them personalized gene therapies which specifically target the tumor. And spotting the defective genes in close relatives who are well, such as daughters, nieces, aunts or cousins, could give them the choice of mitigating risk with preventative surgery.

Dr. Nicola Flaum, lead author on the study from The University of Manchester, said, "This project is the most detailed genetic study of familial ovarian cancer to date.

"And we show that two with a lifetime epithelial ovarian cancer risk of between 5% and 20% are even more present in these families than we thought.

"That is why we think as a matter of routine, women who are BRCA1 and BRCA2 negative with a of ovarian, breast and other cancers should be tested for these other gene mutations.

"Wider genetic testing of women with familial ovarian cancer is essential to both optimize their treatment and enable prevention of disease in family members.

She added, "Ovarian cancer has a poor survival rate as it is usually diagnosed late. That is why it is important to test asymptomatic family members as well so they can be offered risk management strategies.

"We urge patients to tell the doctors about their familial history so they and their relatives can be tested."

More information: Nicola Flaum et al, High detection rate from genetic testing in BRCA-negative women with familial epithelial ovarian cancer, Genetics in Medicine (2022). DOI: 10.1016/j.gim.2022.08.022
Journal information: Genetics in Medicine

Citation: Gene mutations should be tested routinely for ovarian cancer, say scientists (2022, October 4) retrieved 9 December 2022 from https://medicalxpress.com/news/2022-10-gene-mutations-routinely-ovarian-cancer.html
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