4.8 Article

Age-related mutations associated with clonal hematopoietic expansion and malignancies

Journal

NATURE MEDICINE
Volume 20, Issue 12, Pages 1472-1478

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nm.3733

Keywords

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Funding

  1. US National Cancer Institute [R01CA180006, PO1CA101937]
  2. US National Human Genome Research Institute [U54HG003079, U01HG006517]
  3. Leukemia and Lymphoma Society Scholar Award [1230-14]
  4. [R00HL103975]

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Several genetic alterations characteristic of leukemia and lymphoma have been detected in the blood of individuals without apparent hematological malignancies. The Cancer Genome Atlas (TCGA) provides a unique resource for comprehensive discovery of mutations and genes in blood that may contribute to the clonal expansion of hematopoietic stem/progenitor cells. Here, we analyzed blood-derived sequence data from 2,728 individuals from TCGA and discovered 77 blood-specific mutations in cancer-associated genes, the majority being associated with advanced age. Remarkably, 83% of these mutations were from 19 leukemia and/or lymphoma-associated genes, and nine were recurrently mutated (DNMT3A, TET2, JAK2, ASXL1, TP53, GNAS, PPM1D, BCORL1 and SF3B1). We identified 14 additional mutations in a very small fraction of blood cells, possibly representing the earliest stages of clonal expansion in hematopoietic stem cells. Comparison of these findings to mutations in hematological malignancies identified several recurrently mutated genes that may be disease initiators. Our analyses show that the blood cells of more than 2% of individuals (5-6% of people older than 70 years) contain mutations that may represent premalignant events that cause clonal hematopoietic expansion.

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