Vorinostat enhance TRAIL-induced apoptosis via DR5 in anaplastic thyroid cancer cells

被引:1
作者
Liu, Jia [1 ]
Song, Xuesong [2 ]
Xue, Shuai [1 ]
Chen, Guang [1 ]
Dong, Su [2 ]
机构
[1] Jilin Univ, Hosp 1, Dept Thyroid Surg, Changchun, Peoples R China
[2] Jilin Univ, Hosp 1, Dept Anesthesia, Changchun, Peoples R China
来源
2015 7TH INTERNATIONAL CONFERENCE ON INFORMATION TECHNOLOGY IN MEDICINE AND EDUCATION (ITME) | 2015年
关键词
HDACI; Anaplastic thyroid carcinoma; TRAIL; DR5; HISTONE DEACETYLASE INHIBITORS; COLON-CANCER;
D O I
10.1109/ITME.2015.56
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Anaplastic thyroid carcinoma ( ATC) is one of the most aggressive human malignancies, which is refractory to surgery, radiotherapy, radioiodine therapy and conventional chemotherapy. Vorinostat (SAHA, also called suberoylanilide hydroxamic acid) is one of Histone deacetylase inhibitors (HDACIs), which is a promising agent for cancer therapy. Death receptor 5 (DR5) is a transmembrane receptor containing death domain that triggers cell death upon binding to TRAIL (tumor necrosis factor-related apoptosis-inducing ligand), and the combination of TRAIL and agents that increase the expression of DR5 is expected as a novel anticancer therapeutic strategy. Here we report that Vorinostat enhanced TRAIL-induced apoptosis in human anaplastic thyroid cancer cells. This effect is to be achieved through increasing expression of DR5 on the cell surface. Our results provide novel options into the therapy of ATC. We hope that these results could contribute to the advancement of the knowledge of this rare and aggressive cancer.
引用
收藏
页码:302 / 306
页数:5
相关论文
共 12 条
[1]   Anaplastic thyroid carcinoma: Behavior, biology, and therapeutic approaches [J].
Ain, KB .
THYROID, 1998, 8 (08) :715-726
[2]   Histone deacetylase inhibitors induce thyroid cancer-specific apoptosis through proteasome-dependent inhibition of TRAIL degradation [J].
Borbone, E. ;
Berlingieri, M. T. ;
De Bellis, F. ;
Nebbioso, A. ;
Chiappetta, G. ;
Mai, A. ;
Altucci, L. ;
Fusco, A. .
ONCOGENE, 2010, 29 (01) :105-116
[3]   Anaplastic thyroid carcinoma. [J].
Haigh P.I. .
Current Treatment Options in Oncology, 2000, 1 (4) :353-357
[4]   Drug Insight: histone deacetylase inhibitor-based therapies for cutaneous T-cell lymphomas [J].
Khan, Omar ;
La Thangue, Nicholas B. .
NATURE CLINICAL PRACTICE ONCOLOGY, 2008, 5 (12) :714-726
[5]   HDACs and HDAC inhibitors in colon cancer [J].
Mariadason, John M. .
EPIGENETICS, 2008, 3 (01) :28-37
[6]   Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer [J].
Minucci, S ;
Pelicci, PG .
NATURE REVIEWS CANCER, 2006, 6 (01) :38-51
[7]   An antagonist decoy receptor and a death domain-containing receptor for TRAIL [J].
Pan, GH ;
Ni, J ;
Wei, YF ;
Yu, GL ;
Gentz, R ;
Dixit, VM .
SCIENCE, 1997, 277 (5327) :815-818
[8]   Treatment with Panobinostat Induces Glucose-Regulated Protein 78 Acetylation and Endoplasmic Reticulum Stress in Breast Cancer Cells [J].
Rao, Rekha ;
Nalluri, Srilatha ;
Kolhe, Ravindra ;
Yang, Yonghua ;
Fiskus, Warren ;
Chen, Jianguang ;
Ha, Kyungsoo ;
Buckley, Kathleen M. ;
Balusu, Ramesh ;
Coothankandaswamy, Veena ;
Joshi, Atul ;
Atadja, Peter ;
Bhalla, Kapil N. .
MOLECULAR CANCER THERAPEUTICS, 2010, 9 (04) :942-952
[9]   Suberoylanilide hydroxamic acid (Zolinza/vorinostat) sensitizes TRAIL-resistant breast cancer cells orthotopically implanted in BALB/c nude mice [J].
Shankar, Sharmila ;
Davis, Rachel ;
Singh, Karan P. ;
Kurzrock, Razelle ;
Ross, Douglas D. ;
Srivastava, Rakesh K. .
MOLECULAR CANCER THERAPEUTICS, 2009, 8 (06) :1596-1605
[10]  
Sun PC, 2010, BIOCH SCI, V17, P76