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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
1996-2-8
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pubmed:abstractText |
The actual significance of the type of BCR-ABL rearrangement in chronic myeloid leukemia (CML) prognosis remains controversial. Also, the molecular events that lead to CML progression are largely unknown. We analyzed the M-BCR breakpoint position in 64 CML patients by Southern blot and correlated the molecular findings with the cytogenetic, hematologic, and clinical data. No statistically significant differences were found with respect to the clinical and hematologic data presented at diagnosis or in the median duration of chronic phase (CP) and survival between the groups of patients with 5' and 3' breakpoints. We also studied by PCR-SSCP and direct sequencing the p53 gene in patients with specimens available in both chronic phase and blast crisis. We identified p53 mutations in 17% of the blast crisis samples analyzed, whereas no abnormalities were found in CP. This finding suggests that only in a minor fraction of cases are lesions in the p53 gene involved in transformation. Given the present findings, along with previous reports, we believe that a novel mechanism to explain the heterogeneity of CML should be postulated and actively pursued, as should the identification of secondary molecular events more consistently involved in progression.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0165-4608
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
84
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
105-12
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:8536222-Adolescent,
pubmed-meshheading:8536222-Adult,
pubmed-meshheading:8536222-Aged,
pubmed-meshheading:8536222-Base Sequence,
pubmed-meshheading:8536222-Child,
pubmed-meshheading:8536222-DNA Probes,
pubmed-meshheading:8536222-Female,
pubmed-meshheading:8536222-Humans,
pubmed-meshheading:8536222-Leukemia, Myelogenous, Chronic, BCR-ABL Positive,
pubmed-meshheading:8536222-Male,
pubmed-meshheading:8536222-Middle Aged,
pubmed-meshheading:8536222-Molecular Sequence Data,
pubmed-meshheading:8536222-Oncogene Proteins,
pubmed-meshheading:8536222-Polymerase Chain Reaction,
pubmed-meshheading:8536222-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:8536222-Prognosis,
pubmed-meshheading:8536222-Protein-Tyrosine Kinases,
pubmed-meshheading:8536222-Proto-Oncogene Proteins,
pubmed-meshheading:8536222-Proto-Oncogene Proteins c-abl,
pubmed-meshheading:8536222-Proto-Oncogene Proteins c-bcr,
pubmed-meshheading:8536222-Survival Analysis,
pubmed-meshheading:8536222-Transformation, Genetic,
pubmed-meshheading:8536222-Tumor Suppressor Protein p53
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pubmed:year |
1995
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pubmed:articleTitle |
Further evidence for the lack of correlation between the breakpoint site within M-BCR and CML prognosis and for the occasional involvement of p53 in transformation.
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pubmed:affiliation |
Department of Hematology, University of São Paulo, Brazil.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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