� For the first time researchers have proved that there is a genetic susceptibleness to developing chronic lymphocytic leukaemia (CLL), the most common contour of cancer of the blood in the Western earthly concern.
Whilst anecdotal evidence has suggested that inherited factors play a role in the ontogenesis of CLL, scientists suffer until now been unable to prove a transmissible basis.
A study chiefly funded by Leukaemia Research with additional funding from Cancer Research UK and carried verboten at The Institute of Cancer Research has proved that variation in sure genes do play a part and this testament open the way for better treatment of existing patients. It may likewise lead to preventive practice of medicine for the disease in the future.
The results of the research are published in the journal Nature Genetics (31 August).
Close relatives, i.e. siblings, parents or children, of patients with chronic lymphocytic cancer of the blood have a seven-times higher chance of developing this blood crab compared with the general population. For many cancers such as breast cancer, part of the familial risk is caused by a single major disease-risk gene - but no such factor exists for CLL.
The new research has confirmed that the inheritance of a number of low-risk genes john explain role of the inherited susceptibility to develop CLL. Professor Richard Houlston and his team at The Institute of Cancer Research compared DNA from CLL patients with DNA from a healthy grouping. They have found hexad genes with variations in their hereditary sequences that are strongly associated with the development of CLL.
Professor Houlston explains the findings: " This research provides strong evidence that CLL, in at least some cases, is caused by a combination of different genetic variations which ar inherited. Each of these variations, by itself, has a very small event on the risk of developing CLL, but when all of them are present there is a significantly increased risk of leukaemia. Now that we have this evidence we can run out studies to make up one's mind exactly how the different genes contribute to this risk. "
Dr David Grant, Scientific Consultant at Leukaemia Research, says: " This finding is selfsame exciting as it carries the hypothesis of up treatments for individuals world Health Organization we cognize are at risk of developing this leukaemia. Clinical applications ar still a little patch away but this is a very important step forward in understanding the basis of this common leukaemia. "
1. The account is promulgated online from 31 August 2008 in the diary Nature Genetics under the title "A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia". Corresponding author: Dr Richard Houlston, Institute of Cancer Research, Sutton, Surrey.
2. Leukaemia Research provided principal financing for the study. Additional funding was provided by CLL Global Research Foundation, Cancer Research UK, the Arbib fund, and the European Union. Author Dalemari Crowther-Swanepoel (DC-S) was in receipt of a PhD studentship from The Institute of Cancer Research.
3. Chronic lymphocytic leukaemia is a lento progressing var. of leucaemia, characterised by an increased number of white blood cells known as lymphocytes. With about 2,750 new cases occurring each year in the UK, it is the most common chassis of leukaemia and occurs predominantly in late middle age forwards. It has variable symptoms and course, but crataegus oxycantha be diagnosed by probability before the patient develops any clinical symptoms of the disease.
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