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Scientists say they have discovered two genetic variants, which show that both susceptibility and survival of childhood leukemia can be inherited, according to a study published in the journal Blood.
Researchers from The Institute of Cancer Research in London say the discovery could lead to new drugs for children who do not respond well to current treatments for the disease.
Childhood acute lymphoblastic leukemia (ALL) is the most common cancer in children and teens, occurring when the bone marrow makes too many immature lymphocytes - a type of white blood cell. Onset is most common between 2 and 4 years of age.
For the study, the researchers analyzed the genomes of more than 1,500 children with leukemia, alongside 4,500 healthy children.
Results of the analysis revealed a strong link between two common single nucleotide polymorphisms (SNPs) - "copying errors" in DNA - with susceptibility to leukemia.
The researchers say that one of the SNPs, called rs3824662 and found in the gene GATA3, was linked to a tumor subtype known to have two-fold increased rates of relapse and poorer overall survival.
Richard Houlston, professor of molecular and population genetics at The Institute of Cancer Research and lead author of the study, told Medical News Today:
"These findings are very significant because they provide additional evidence for inherited susceptibility to developing childhood acute lymphoblastic leukemia.
Moreover, one of the SNPs is also linked to the risk of development a specific form of ALL, which has a poor prognosis. This finding provides new insights into how ALL develops."
According to the American Cancer Society, childhood leukemia survival rates have greatly increased over time, and a 5-year survival rate for ALL is now more than 85%.
However, the researchers add that although treatments for the disease have come a long way, there are still a number of patients who do not respond well to them.
"These findings provide further insights into the genetic and biological basis of inherited genetic susceptibility to childhood acute lymphoblastic leukemia," says Chris Bunce, research director at Leukemia and Lymphoma Research, who funded the study.
"By understanding how different genetic variations determine cancer subtype, we can tailor treatment accordingly," he adds.
Prof. Houlston says:
"In the long term, the knowledge about the genes and pathways key to the development of ALL is likely to be highly informative in designing novel therapies and in tailoring patient treatment."
A recent study, also from The Institute of Cancer Research, identified the first mutations within a mother's womb that lead to the onset of leukemia, which they said could lead to the development of new treatments.
Scientists from St. Jude Children's research Hospital recently revealed they have identified a protein that certain cells at high risk for acute lymphoblastic leukemia need to survive, leading to a new strategy for killing tumor cells.
Written by Honor Whiteman
Copyright: Medical News Today
Not to be reproduced without the permission of Medical News Today.
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype, published in the journal Blood, 30 August 2013.
Visit our Lymphoma / Leukemia / Myeloma category page for the latest news on this subject.
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