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Genetic Screens Provide Clues About Prognosis, Risk of Second Cancer

Mutations in the TP53 gene appear to influence the prognosis and likelihood of future cancers in pediatric leukemia patients.

Written byShawna Williams
| 5 min read

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BIG SCREEN: Cancer researcher Jun Yang of St. Jude Children’s Research Hospital and his colleagues combed through data on 3,801 children with ALL.ST. JUDE/SETH DIXON

There are cancers with mutated genes, and then there’s hypodiploid acute lymphoblastic leukemia (ALL). This rare subtype of ALL, a childhood leukemia, is characterized by deletions of whole chromosomes—and worse survival rates than other subtypes. More than 90 percent of ALL patients, but fewer than half of pediatric hypodiploid ALL patients, survive with treatment. In 2013, researchers at St. Jude Children’s Research Hospital and colleagues looked into whether there was anything distinctive about the gene variants carried by patients with hypodiploid leukemia. Within a cohort they examined, they found, first, that the subtype itself has two subtypes; and then, in one of those, called low hypodiploid ALL, 91 percent of patients carried certain variants of the TP53 gene, which codes for the tumor-suppressing protein p53 ...

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Meet the Author

  • Shawna was an editor at The Scientist from 2017 through 2022. She holds a bachelor’s degree in biochemistry from Colorado College and a graduate certificate in science communication from the University of California, Santa Cruz. Previously, she worked as a freelance editor and writer, and in the communications offices of several academic research institutions. As news director, Shawna assigned and edited news, opinion, and in-depth feature articles for the website on all aspects of the life sciences. She is based in central Washington State, and is a member of the Northwest Science Writers Association and the National Association of Science Writers.

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