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PMID: 10891474 Published · ppublish English Clinical Trial Controlled Clinical Trial Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Telomere length shortening in chronic myelogenous leukemia is associated with reduced time to accelerated phase.

Blood ·Vol. 96 ·No. 1 ·2000-07-01 ·Pages 358-61

Boultwood J, Peniket A, Watkins F, Shepherd P, McGale P, Richards S, Fidler C, Littlewood TJ, Wainscoat JS

Abstract

Telomere shortening is associated with disease evolution in chronic myelogenous leukemia (CML). We have examined the relationship between diagnostic telomere length and outcome in 59 patients with CML who entered into the MRC CMLIII Trial by Southern blot hybridization using the (TTAGGG)(4) probe. Age-adjusted telomere repeat array (TRA) reduction was found to significantly correlate with time from diagnosis to acceleration, such that patients with a larger TRA reduction entered the accelerated phase more rapidly (r = -0.50; P =.008). Cox-regression analysis for this group was suggestive of a relationship between a greater TRA-reduction and a shorter time to acceleration (P =.054). Age-adjusted TRA reduction did not significantly affect either the time to blast crisis or overall survival. Our results show that telomere shortening observed at the time of diagnosis in CML significantly influences the time to progress to the accelerated phase. The measurement of diagnostic TRA may prove to be clinically important in the selection of patients at high risk of disease transformation in CML.

MeSH Terms
Age Factors Antineoplastic Agents/therapeutic use Biomarkers, Tumor Blast Crisis Blotting, Southern Humans Interferon-alpha/therapeutic use Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy,genetics,mortality,pathology Oligonucleotide Probes Platelet Count Regression Analysis Spleen/pathology Survival Rate Telomere/ultrastructure
Chemicals
Antineoplastic Agents Biomarkers, Tumor Interferon-alpha Oligonucleotide Probes
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Boultwood J
Leukaemia Research Fund Molecular Haematology Unit, Department of Cellular Science, John Radcliffe Hospital, Oxford, UK. [email protected]
Peniket A
Watkins F
Shepherd P
McGale P
Richards S
Fidler C
Littlewood T J
Wainscoat J S
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2000-07-01
Pages
358-61
Language
English
Region
United States
NLM ID
7603509
Subset
IM
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