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You are here: Home > Cancer > Rare tumour’s ‘fingerprint’ used to develop cheap and reliable new test

Rare tumour’s ‘fingerprint’ used to develop cheap and reliable new test

23 May 2011 · Listed under Cancer

Researchers at the University of Oxford have developed a cheap and reliable diagnostic test for a rare form of cancer. The test involves screening tumour samples for a particular molecular fingerprint unique to this cancer.

Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a disorder that causes the development of benign but often painful tumours in the skin and, in females, in the uterus. Between one in six and one in ten people affected by the disorder will go on to develop an aggressive form of kidney cancer called papillary renal cell cancer. The condition often strikes people in their 20s.

The disorder is caused by mutations, which may be inherited, in a gene responsible for the production of an enzyme known as fumarate hydratase (FH). This leads to an accumulation within cells of fumarate, which promotes the development of cancer cells.

Now, in a study published in the ‘Journal of Pathology’, an international team of scientists led by researchers at the Henry Wellcome Building for Molecular Physiology, University of Oxford, have identified a particular protein modification that is induced by FH deficiency (and hence an over-abundance of fumarate). This alteration is unique to this type of tumour and can hence be used as a biomarker – a biological ‘fingerprint’ to identify tumours caused by this mechanism.

The researchers have developed a test for this protein modification that can be carried out in under two hours and will identify tumours with FH mutations. This approach is much more cost-effective than genetic testing of all possible cases using DNA sequencing. They show that screening cases of papillary renal cell cancer using this new test allows them to identify undiagnosed cases of HLRCC for genetic testing. They believe this test should be applied in all cases of papillary renal cell cancer to identify people with FH mutations, allowing advice to be provided to their families on their own relative risks of developing the disorder and associated kidney cancer.

Click here for full article.

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