{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,10]],"date-time":"2026-06-10T15:11:04Z","timestamp":1781104264657,"version":"3.54.1"},"reference-count":47,"publisher":"National Academy of Sciences","issue":"18","content-domain":{"domain":["www.pnas.org"],"crossmark-restriction":true},"short-container-title":["Proc. Natl. Acad. Sci. U.S.A."],"published-print":{"date-parts":[[2001,8,28]]},"abstract":"<jats:p>\n                    Therapy-related acute myeloid leukemias (t-AML) with translocations of the\n                    <jats:italic>MLL<\/jats:italic>\n                    gene are associated with the use of topoisomerase II inhibitors. We established the emergence of the malignant clone in a child who developed t-AML with a t(11;19) (q23;p13.3) during treatment for acute lymphoblastic leukemia (ALL). The\n                    <jats:italic>MLL-ENL<\/jats:italic>\n                    and the reciprocal\n                    <jats:italic>ENL-MLL<\/jats:italic>\n                    genomic fusions and their chimeric transcripts were characterized from samples collected at the time of t-AML diagnosis. We used PCR with patient-specific genomic primers to establish the emergence of the\n                    <jats:italic>MLL-ENL<\/jats:italic>\n                    fusion in serially obtained DNA samples. The\n                    <jats:italic>MLL-ENL<\/jats:italic>\n                    fusion was not detectable in bone marrow at the time of ALL diagnosis or after 2 months of chemotherapy (frequency &lt;8.3 \u00d7 10\n                    <jats:sup>\u22127<\/jats:sup>\n                    cells\n                    <jats:sup>\u22121<\/jats:sup>\n                    ). The genomic fusion was first detected in bone marrow after 6 months of treatment at a frequency of one in 4,000 mononuclear bone marrow cells; the frequency was one in 70 cells after 20 months of therapy. At the first detection of\n                    <jats:italic>MLL-ENL<\/jats:italic>\n                    , the only topoisomerase II inhibitors the patient had received were one dose of daunorubicin and two doses of etoposide. The\n                    <jats:italic>MLL-ENL<\/jats:italic>\n                    fusion was not detectable in blood at the time of ALL diagnosis or after 0.7, 2, 8, 10, and 12 months of therapy but was detectable in blood at 16 months (one in 2.3 \u00d7 10\n                    <jats:sup>4<\/jats:sup>\n                    cells). Recombinogenic\n                    <jats:italic>Alu<\/jats:italic>\n                    sequences bracketed the breakpoints in both fusions. These data indicate that the malignant clone was not present before therapy, arose early during chemotherapy, and was able to proliferate even during exposure to antileukemic therapy.\n                  <\/jats:p>","DOI":"10.1073\/pnas.181199898","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T10:45:09Z","timestamp":1027680309000},"page":"10338-10343","update-policy":"https:\/\/doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":52,"title":["Molecular emergence of acute myeloid leukemia during treatment for acute lymphoblastic leukemia"],"prefix":"10.1073","volume":"98","author":[{"given":"Javier G.","family":"Blanco","sequence":"first","affiliation":[{"name":"Departments of Pharmaceutical Sciences, Hematology\u2013Oncology, Pathology, and Hartwell Center for Bioinformatics and Biotechnology, St. Jude Children's Research Hospital, 332 North Lauderdale, Memphis, TN 38105; and University of Tennessee, Colleges of Pharmacy 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