News Release

Research suggests statins could lower ovarian cancer risk

Peer-Reviewed Publication

Cancer Research UK

A genetic study has found evidence to suggest that women who take statins in the long term could be less likely to develop ovarian cancer, according to new research funded by Cancer Research UK published today (Tuesday 18 February)*.

The same result was also found in women who carry the BRCA1/2 gene fault. Having the BRCA1/2 fault puts women at a higher risk of ovarian cancer than the general population**.

The research published in JAMA studied genes and the extent to which they inhibit the enzyme HMG-CoA reductase - which is responsible for regulating cholesterol in the body - and is the exact enzyme targeted by statin drugs to reduce cholesterol.

While the study suggests that statins could lower ovarian cancer risk, more research needs to be done specifically looking at their use and impact on women's risk of developing the disease.

The researchers based at the University of Bristol looked at 63,347 women between the ages of 20 and 100 years old, of whom 22,406 had ovarian cancer. They also looked at an additional 31,448 women who carried the BRCA1/2 fault, of whom 3,887 had ovarian cancer. The study used an approach called Mendelian randomization***, which involves analysing the genetic data from thousands of people.

Statins may protect against the development of ovarian cancer because they've been shown to induce apoptosis - one of the body's ways of getting rid of old, faulty or infected cells - and to stop tumours from growing in laboratory studies. Another line of thought is that statins lower circulating cholesterol, which helps regulate cell growth, though this research suggests that lower circulating cholesterol was not the method by which statins may reduce ovarian cancer risk.

The findings suggest that long-term statin use could be associated with an estimated 40% reduction in ovarian cancer risk in the general population, although the estimate comes from looking at gene variation rather than statins themselves, and the exact mechanism by which these genes are associated with lower ovarian cancer risk is unclear.

Ovarian cancer is the 6th most common cancer in women in the UK. There are around 7,400 cases each year****, and out of those with a known stage at diagnosis, almost 6 in 10 are diagnosed at a late stage*****. Around 4,100 women die from the disease every year in the UK.

There is no test that reliably picks up ovarian cancer at an early stage, so chemoprevention could be an important approach to saving lives.

Professor Richard Martin, from the University of Bristol, said: "Our findings open up the possibility of repurposing a cheap drug to help prevent ovarian cancer - especially in women who are at a higher risk. It's incredibly interesting that women whose bodies naturally inhibit the enzyme targeted by statins have a lower risk of ovarian cancer, but we don't recommend anyone rushes to take statins specifically to reduce ovarian cancer risk because of this study.

"It's a promising result and I hope it sparks more research and trials into statins to demonstrate conclusively whether or not there's a benefit."

Dr Rachel Orritt, Cancer Research UK's health information manager, said: "This study is a great first step to finding out if statins could play a role in lowering ovarian cancer risk, and justifies future research into this area.

"But there's not yet enough evidence to know if statins themselves could reduce the risk of developing ovarian cancer safely. And it's important to remember that the risk of developing ovarian cancer depends on many things including age, genetics and environmental factors. Speak to your doctor first if you have any concerns about your risk."

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For media enquiries please contact Laurence Leong in the Cancer Research UK press office on 020 3469 8398 or, out of hours, 07050 264 059.

Notes to editor:

*Yarmolinsky J, et al, Association between genetically-proxied inhibition of HMG-CoA reductase and epithelial ovarian cancer, JAMA, 2020

** More than 4 in 10 women with faults in BRCA1, and less than 2 in 10 women with BRCA2 faults, are estimated to develop ovarian cancer by age 80: Kuchenbaecker K, et al, Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers, JAMA, 2017

***More information on Mendelian randomization can be found in a previous Cancer Research UK science blog: https://scienceblog.cancerresearchuk.org/2018/05/17/could-mother-natures-clinical-trial-help-prevent-more-cancers/

**** Based on the average annual number of new cases of ovarian cancer (ICD10 C56-57.4) diagnosed in the UK between 2015 and 2017.

*****Late-stage defined as stage 3 or 4. Statistics based on known stage distribution data for ovarian cancers diagnosed in England in 2017 and the average number of ovarian cancers diagnosed in Northern Ireland between 2013 and 2017.

Sources:

England: http://www.ncin.org.uk/publications/survival_by_stage

Northern Ireland: http://www.qub.ac.uk/research-centres/nicr/CancerInformation/official-statistics/BySite/Ovary/


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