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Clinical Translational Research

Histone Deacetylase in Chronic Lymphocytic Leukemia

Wang J.C.a · Kafeel M.I.a · Avezbakiyev B.a · Chen C.a · Sun Y.a · Rathnasabapathy C.a · Kalavar M.a · He Z.a · Burton J.b · Lichter S.a

Author affiliations

aDivision of Hematology/Oncology, Brookdale University Hospital Medical Center, and bDivision of Hematology/Oncology, Coney Island Hospital, Brooklyn, N.Y., USA

Related Articles for ""

Oncology 2011;81:325–329

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Article / Publication Details

First-Page Preview
Abstract of Clinical Translational Research

Received: July 26, 2011
Accepted: October 19, 2011
Published online: January 10, 2012
Issue release date: February 2012

Number of Print Pages: 5
Number of Figures: 2
Number of Tables: 2

ISSN: 0030-2414 (Print)
eISSN: 1423-0232 (Online)

For additional information: https://www.karger.com/OCL

Abstract

Background: Elevated histone deacetylase (HDAC) isoenzyme levels have been described in patients with carcinomas and leukemias. HDAC inhibitors (HDACi) have shown promise in the treatment of carcinomas and are currently under intense research. To make better use of HDACi in treating chronic lymphocytic leukemia (CLL), HDAC isoenzyme levels were studied. Methods: Quantitative reverse transcriptase polymerase chain reaction for HDAC isoenzyme was measured in 32 patients with CLL and compared with 17 normal volunteer controls. ZAP-70, CD38 and CD44 were also assayed and correlated to HDAC isoenzyme levels. Results: The results showed: (1) HDAC isoenzyme levels in CLL were significantly increased in class I including HDAC1 and HDAC3, in class II including HADC6, HDAC7, HDAC9 and HDAC10, and in class III including SIRT1 and SIRT6; (2) higher expression of HDAC isoenzyme levels was found in ZAP-70+ compared to ZAP-70– patients, and CD44 expression levels were correlated with HDAC isoenzyme expression levels in the majority of HDAC classes. Conclusions: These results suggest: (1) in CLL, elevated HDAC isoenzyme activity is not restricted to one class, and therefore, HDACi therapy may need to be directed to more than one specific class of HDAC; (2) higher HDAC expression activity may indicate a poor prognosis and more advanced disease stage (through indirect evidence), since higher values were found in patients with ZAP-70+ and higher CD44 expression levels.

© 2012 S. Karger AG, Basel


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    External Resources
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Article / Publication Details

First-Page Preview
Abstract of Clinical Translational Research

Received: July 26, 2011
Accepted: October 19, 2011
Published online: January 10, 2012
Issue release date: February 2012

Number of Print Pages: 5
Number of Figures: 2
Number of Tables: 2

ISSN: 0030-2414 (Print)
eISSN: 1423-0232 (Online)

For additional information: https://www.karger.com/OCL


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