pubmed-article:9089742 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9089742 | lifeskim:mentions | umls-concept:C1705280 | lld:lifeskim |
pubmed-article:9089742 | lifeskim:mentions | umls-concept:C0023452 | lld:lifeskim |
pubmed-article:9089742 | lifeskim:mentions | umls-concept:C0249219 | lld:lifeskim |
pubmed-article:9089742 | lifeskim:mentions | umls-concept:C0525037 | lld:lifeskim |
pubmed-article:9089742 | lifeskim:mentions | umls-concept:C0017260 | lld:lifeskim |
pubmed-article:9089742 | lifeskim:mentions | umls-concept:C0809183 | lld:lifeskim |
pubmed-article:9089742 | lifeskim:mentions | umls-concept:C2362057 | lld:lifeskim |
pubmed-article:9089742 | lifeskim:mentions | umls-concept:C2826293 | lld:lifeskim |
pubmed-article:9089742 | lifeskim:mentions | umls-concept:C0021149 | lld:lifeskim |
pubmed-article:9089742 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:9089742 | pubmed:dateCreated | 1997-5-27 | lld:pubmed |
pubmed-article:9089742 | pubmed:abstractText | We have examined the incidence and clinical significance of deletions of two candidate tumor suppressor genes, CDKN2/MTS1/p16ink4A and MTS2/p15ink4B, in pediatric acute lymphoblastic leukemia (ALL). Gene deletion was evaluated in leukemic bone marrow (BM) cells obtained at diagnosis from 105 pediatric ALL patients: 83 with B-cell precursor (BCP-ALL) ALL and 22 with T-ALL. CDKN2/p16 deletion was seen in 23 of the 83 (28%) BCP-ALL and 15 of the 22 (68%) T-ALL cases. A virtually identical pattern of MTS2/p15 deletion was detected in these patients: p15 was deleted in 37 of 38 cases with p16 deletion, and p15 was not deleted in any p16-positive specimens. P16/p15 deletions were significantly related to poor prognosis factors including age under 1 year (P < 0.001), initial white cell counts greater than 50 x 10(9) per liter (P < .001), and T cell phenotype P < .005). Analysis of all 105 patients revealed that the 5-year disease-free survival rate was 68% for patients without p16/p15 deletions and 35% for those with p16/p15 deletions (P < .005). The association between gene deletion at initial diagnosis and unfavorable outcome suggests that loss of these genes is clinically significant and indicates a need for prospective studies of p16/p15 deletion in pediatric ALL patients. | lld:pubmed |
pubmed-article:9089742 | pubmed:language | eng | lld:pubmed |
pubmed-article:9089742 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9089742 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:9089742 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9089742 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9089742 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9089742 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9089742 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9089742 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9089742 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9089742 | pubmed:issn | 0888-0018 | lld:pubmed |
pubmed-article:9089742 | pubmed:author | pubmed-author:JL | lld:pubmed |
pubmed-article:9089742 | pubmed:author | pubmed-author:YeagerA MAM | lld:pubmed |
pubmed-article:9089742 | pubmed:author | pubmed-author:ZhouMM | lld:pubmed |
pubmed-article:9089742 | pubmed:author | pubmed-author:FindleyH WHW | lld:pubmed |
pubmed-article:9089742 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9089742 | pubmed:volume | 14 | lld:pubmed |
pubmed-article:9089742 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9089742 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9089742 | pubmed:pagination | 141-50 | lld:pubmed |
pubmed-article:9089742 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:9089742 | pubmed:articleTitle | Incidence and clinical significance of CDKN2/MTS1/P16ink4A and MTS2/P15ink4B gene deletions in childhood acute lymphoblastic leukemia. | lld:pubmed |
pubmed-article:9089742 | pubmed:affiliation | Division of Pediatric Hematology/Oncology/Bone Marrow Transplantation, Emory University School of Medicine, Atlanta, Georgia 30322, USA. | lld:pubmed |
pubmed-article:9089742 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:9089742 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:9089742 | lld:pubmed |