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A Histone Deacetylase Inhibitor LBH589 Downregulates XIAP in Mesothelioma Cell Lines Which is Likely Responsible for Increased Apoptosis With TRAIL

A Histone Deacetylase Inhibitor LBH589 Downregulates XIAP in Mesothelioma Cell Lines Which is... ORIGINAL ARTICLE A Histone Deacetylase Inhibitor LBH589 Downregulates XIAP in Mesothelioma Cell Lines Which is Likely Responsible for Increased Apoptosis With TRAIL James Symanowski, PhD,* Nicholas Vogelzang, MD,* Leigh Zawel, PhD,† Peter Atadja, PhD,† Harvey Pass, MD,‡ and Sunil Sharma, MD* Key Words: Mesothelioma, Histone deacetylase inhibitors, apopto- Purpose: Tumor necrosis factor-alpha-related apoptosis-inducing sis, Tumor necrosis factor-alpha-related apoptosis-inducing ligand. ligand (TRAIL) is a member of tumor necrosis factor family and it (J Thorac Oncol. 2009;4: 149–160) is important for ligand induced apoptosis in tumor cells. TRAIL has been shown to be synergistic with a variety of chemotherapies and targeted agents. In the study, a combination of TRAIL and a histone umor necrosis factor-alpha-related apoptosis-inducing li- deacetylase inhibitor LBH589 was studied in mesothelioma cell Tgand (TRAIL) is a member of tumor necrosis factor lines. (TNF) superfamily and exhibits antitumor activity in a vari- Experimental Design: Five mesothelioma cell lines and two normal 1,2 1,2 ety of tumor cells. TRAIL signals primarily through two cell lines were tested for cell growth inhibition and apoptosis using receptors—DR4 and DR5 that carry a cytoplasmic death high-throughput assays in the presence of LBH589, TRAIL and a domain. Upon binding to its receptors, TRAIL induces http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Journal of Thoracic Oncology Wolters Kluwer Health

A Histone Deacetylase Inhibitor LBH589 Downregulates XIAP in Mesothelioma Cell Lines Which is Likely Responsible for Increased Apoptosis With TRAIL

Journal of Thoracic Oncology , Volume 4 (2) – Feb 1, 2009

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ISSN
1556-0864
DOI
10.1097/JTO.0b013e318194f991
pmid
19179889
Publisher site
See Article on Publisher Site

Abstract

ORIGINAL ARTICLE A Histone Deacetylase Inhibitor LBH589 Downregulates XIAP in Mesothelioma Cell Lines Which is Likely Responsible for Increased Apoptosis With TRAIL James Symanowski, PhD,* Nicholas Vogelzang, MD,* Leigh Zawel, PhD,† Peter Atadja, PhD,† Harvey Pass, MD,‡ and Sunil Sharma, MD* Key Words: Mesothelioma, Histone deacetylase inhibitors, apopto- Purpose: Tumor necrosis factor-alpha-related apoptosis-inducing sis, Tumor necrosis factor-alpha-related apoptosis-inducing ligand. ligand (TRAIL) is a member of tumor necrosis factor family and it (J Thorac Oncol. 2009;4: 149–160) is important for ligand induced apoptosis in tumor cells. TRAIL has been shown to be synergistic with a variety of chemotherapies and targeted agents. In the study, a combination of TRAIL and a histone umor necrosis factor-alpha-related apoptosis-inducing li- deacetylase inhibitor LBH589 was studied in mesothelioma cell Tgand (TRAIL) is a member of tumor necrosis factor lines. (TNF) superfamily and exhibits antitumor activity in a vari- Experimental Design: Five mesothelioma cell lines and two normal 1,2 1,2 ety of tumor cells. TRAIL signals primarily through two cell lines were tested for cell growth inhibition and apoptosis using receptors—DR4 and DR5 that carry a cytoplasmic death high-throughput assays in the presence of LBH589, TRAIL and a domain. Upon binding to its receptors, TRAIL induces

Journal

Journal of Thoracic OncologyWolters Kluwer Health

Published: Feb 1, 2009

References