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            <title xml:lang="en">Screening for leukemia- and clone-specific markers at birth in children with T cell precursor ALL suggests a predominantly postnatal origin.</title>
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                <forename type="first">Susanna</forename>
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                <forename type="first">Oskar A</forename>
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                <forename type="first">E Renate</forename>
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              <date type="whenSubmitted">2007-07-26 14:39:40</date>
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              <date type="whenReleased">2007-07-26 14:39:40</date>
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                <title xml:lang="en">Screening for leukemia- and clone-specific markers at birth in children with T cell precursor ALL suggests a predominantly postnatal origin.</title>
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                  <persName>
                    <forename type="first">Susanna</forename>
                    <surname>Fischer</surname>
                  </persName>
                  <idno type="halauthorid">221088-0</idno>
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                <author role="aut">
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                    <forename type="first">Georg</forename>
                    <surname>Mann</surname>
                  </persName>
                  <idno type="halauthorid">221089-0</idno>
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                <author role="aut">
                  <persName>
                    <forename type="first">Marianne</forename>
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                  <idno type="halauthorid">221091-0</idno>
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                <author role="aut">
                  <persName>
                    <forename type="first">Georg</forename>
                    <surname>Ebetsberger</surname>
                  </persName>
                  <idno type="halauthorid">221092-0</idno>
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                <author role="aut">
                  <persName>
                    <forename type="first">Neil</forename>
                    <surname>Jones</surname>
                  </persName>
                  <idno type="halauthorid">221093-0</idno>
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                    <forename type="first">Bertrand</forename>
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                  <persName>
                    <forename type="first">Oskar A</forename>
                    <surname>Haas</surname>
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                <author role="aut">
                  <persName>
                    <forename type="first">Klaus</forename>
                    <surname>Schmitt</surname>
                  </persName>
                  <idno type="halauthorid">221096-0</idno>
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                <author role="aut">
                  <persName>
                    <forename type="first">E Renate</forename>
                    <surname>Panzer-Grumayer</surname>
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                <title level="j">Blood</title>
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                  <publisher>American Society of Hematology</publisher>
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                  <date type="datePub">2007-06-08</date>
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              <p>Childhood T cell precursor (TCP) ALL is an aggressive disease with a presumably short latency that differs in many biological respects from B cell precursor (BCP) ALL. We therefore addressed the issue of in utero origin of this particular type of leukemia by tracing oncogenic mutations and clone-specific molecular markers back to birth. These markers included various first and second hit genetic alterations (TCRD-LMO2 breakpoint regions, n=2; TAL1 deletions, n=3; Notch1 mutations, n=1), and non-oncogenic T cell receptor rearrangements (n=13) that were derived from leukemias of 16 children, who were 1,5 - 11,2 years old at diagnosis of leukemia. Despite highly sensitive PCR approaches (one cell with a specific marker among 100.000 normal cells), we identified the leukemic clone in the neonatal blood spots in only one young child. These data suggests that in contrast to BCP ALL the vast majority of TCP ALL cases are initiated after birth.</p>
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