Linked Life Data

8127144

Source:http://linkedlifedata.com/resource/pubmed/id/8127144

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1994-4-12
pubmed:abstractText
The polymerase chain reaction (PCR) is more sensitive than other methods for detecting residual leukemic cells, and it can be used to analyze the dynamics of the leukemic cell population during and after chemotherapy. Leukemia cells are identified among the normal cells through the use of a leukemic cell-specific signature, such as the junction formed following rearrangement of the immunoglobulin (Ig) or T-cell receptor (TCR) variable (V), diversity (D), and joining (J) regions. We cloned the rearranged Ig or TCR genes from leukemic cells at the time of diagnosis by regular recombinant DNA techniques, or following PCR amplification, and determined the leukemic cell-specific V(D)J junctions. Using oligonucleotides prepared to the unique junctional sequences, we have analyzed Southern blots of PCR-amplified Ig or TCR genes from 11 patients at the time of diagnosis, and in from three to 14 follow-up samples for periods ranging from 17 to 97 months. The level of detection of residual blast cells in these patients was usually on the order of 1 leukemic cell in 10(4) normal ones. Conditions for the hybridization and washing were individually adjusted so that the specificity of the probes was excellent. No residual leukemic cells were found in patients who remained in continuous complete remission at time points more than 6 months post-diagnosis. PCR detected impending relapse in four out of six cases, with PCR-detectable leukemic clones being present 2, 4, 13 and 20 months prior to clinical signs of the disease. Relapse occurred in two patients who lacked PCR evidence of leukemic blasts in marrow samples collected 2 and 6 months before clinical recurrence, respectively. The leukemic cells that persisted for 3 years after a relapse in a patient who remained in clinical remission during this time period eventually became undetectable by PCR.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0887-6924
pubmed:author
pubmed:issnType
Print
pubmed:volume
8
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
395-401
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed:year
1994
pubmed:articleTitle
Residual disease detection in multiple follow-up samples in children with acute lymphoblastic leukemia.
pubmed:affiliation
Department of Virology and Molecular Biology, St Jude Children's Research Hospital, Memphis, TN 38101.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't