Inherited Genetic Variant Increases Risk of Chronic Lymphocytic Leukemia

They found that a single letter DNA sequence variation, known as a single nucleotide polymorphism (SNP), at a specific site in the genome disrupts the activity of a protein called Transcription factor p65 or RELA. This protein is involved in a process of controlled cell death that is a key part of the body's natural defense against disease.

The investigators used published GWAS CLL data to scan 517 cases using HumanCNV370-Duo BeadChips (Illumina, San Diego, CA, USA) with Hap1.2M-Duo Custom array data on 2,698 individuals as controls. Others techniques used included epigenetic annotation, plasmid construction and luciferase assays analyzed on a Fluoroskan Ascent FL plate reader (Thermo Fisher Scientific, Waltham, MA, USA), and gene expression and splicing analysis.

The team found that the particular risk SNP, rs539846-A, interferes with the activity switch of a gene, called 'BCL-2 modifying factor' (BMF), that normally works to produce 'pro-death' signals. This makes it harder for RELA to flip on the activity of the gene and reduces the levels of the signal. This loss of 'pro-death' signal tips the balance towards 'pro-survival', so that the CLL cells can sidestep self-destruction. These findings complement work from recent clinical trials that showed drugs that mimic 'pro-death' proteins by targeting the 'pro-survival' BCL-2 pathway can produce a strong anti-cancer effect in CLL patients who had relapsed after initial treatment. The latest discovery could provide important insight into how these and similar drugs work so that their combined use can be optimized.

Richard S. Houlston, MD, PhD, a Professor of Molecular and Population Genetics, and lead investigator said, “Although many significant risk variants for this type of leukemia have been identified, the biological mechanisms through which these variants affect leukemia development have been less well studied. This study highlights the importance of cell death-inducing proteins such as BMF in controlling CLL development and could help in the design of new drugs to treat this disease.” The study was published on August 11, 2016, in the journal Cell Reports.

Related Links:
The Institute of Cancer Research
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