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P15INK4B gene methylation and expression in normal, myelodysplastic, and acute myelogenous leukemia cells and in the marrow cells of cured lymphoma patients

  • H. D. Preisler
    ,
  • Biaoru Li
    ,
  • H. Chen
    ,
  • L. Fisher
    ,
  • J. Nayini
    ,
  • A. Raza
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

P15INK4B methylation and expression was studied in bone marrow cells obtained from normal individuals, from patients who had been cured of lymphoma, and from patients with either MDS or AML. The level of p15 methylation was very low in normal BM cells and in CD34+ and CD34− subpopulations (0-6.5%; med, = 2.5%). P15INK4B transcripts were present in each of these cell populations. In contrast, methylation was the usual situation in MDS and AML marrows. The presence of methylation of the p15INK4B gene did not always indicate an absence of expression nor was expression always present if methylation was absent. P15INK4B methylation was studied in the marrows of nine patients (one studied twice) who had been cured of lymphoma and in whom hemopoiesis was believed to be normal. Increased methylaton was present in all 10 marrows. These data indicate that p15INK4B methylation is likely to be a very early event in the development of the secondary hematologic disorders.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1589-1595 (7 pages)

Journal (Volume, Issue Number)

Leukemia (Volume 15, Issue 10)

Publication milestones

  • Published - 2001

Publication status

Published - 2001

ISSN

0887-6924

Publication IDs

  • Scopus: 0034740657
  • PubMed: 11587217

Publication metrics

Metrics

Scopus
citations
SciVal
citations
37
Fractional count
1
Fractional count
0.13
Fractional count
7
Fractional count
0.88
Fractional count
1
Fractional count
1
SciVal
FWCI
0.96
SciVal
Author count
8
SciVal
Paper percentile
81

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Citation count
37
Captures
10

Funding Details

This work was supported by the National Cancer Institute grant 1-PO-1CA75606-04.
FunderFunding numbers
NCI
1-PO-1CA75606-04, P01CA075606