New type of Bcr/Abl junction in Philadelphia chromosome-positive chronic myelogenous leukemia.

نویسندگان

  • G Saglio
  • A Guerrasio
  • C Rosso
  • A Zaccaria
  • A Tassinari
  • A Serra
  • G Rege-Cambrin
  • U Mazza
  • F Gavosto
چکیده

A new and rare type of Bcr/Abl junction between exon C3 of the 3' portion of the Bcr gene and Abl exon 2 has been identified in the leukemic cells of two Ph1-positive chronic myelogenous leukemia patients in chronic phase. This is the fourth type of Bcr/Abl junction so far identified in Ph1-positive hematologic malignancies and is a consequence of an unusual breakpoint position on chromosome 22 that falls approximately 20 kb downstream of the major breakpoint cluster region (bcr) of the Bcr gene. The new hybrid mRNA is 540 base pairs (bp) longer than that expressed by the K562 cell line and could codify for a Bcr/Abl protein carrying 180 additional aminoacids with respect to the larger P210 protein so far identified. The hematologic phenotype expressed by the two patients carrying this unusual type of Bcr/Abl rearrangement does not significantly differ from that commonly seen in chronic myelogenous leukemia.

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New Type of B c r / A b f Junction in Philadelphia Chromosome - Positive Chronic Myelogenous Leukemia

A new and rare type of Bcr/Abl junction between exon C3 of the 3‘ portion of the Bcr gene and Ab1 exon 2 has been identified in the leukemic cells of two Ph‘-positive chronic myelogenous leukemia patients in chronic phase. This is the fourth type of Bcr/Abl junction so far identified in Phl-positive hematologic malignancies and is a consequence of an unusual breakpoint position on chromosome 22...

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Novel types of bcr-abl transcript with breakpoints in BCR exon 8 found in Philadelphia positive patients with typical chronic myeloid leukemia retain the sequence encoding for the DBL- and CDC24 homology domains but not the pleckstrin homology one.

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BCR-ABL rearrangements in children with Philadelphia chromosome-positive chronic myelogenous leukemia.

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BCR-ABL fusion transcript types and levels and their interaction with secondary genetic changes in determining the phenotype of Philadelphia chromosome-positive leukemias.

It remains unresolved how different BCR-ABL transcripts differentially drive lymphoid and myeloid proliferation in Philadelphia chromosome-positive (Ph(+)) leukemias. We compared BCR-ABL transcript type and level with kinase domain (KD) mutation status, genotype, and phenotype in 1855 Ph(+) leukemias. Compared with e1a2/p190 BCR-ABL cases, de novo e13-e14a2/p210 Ph(+) lymphoid leukemia more fre...

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عنوان ژورنال:
  • Blood

دوره 76 9  شماره 

صفحات  -

تاریخ انتشار 1990