HDAC5 promotes osteosarcoma progression by upregulation of Twist 1 expression

被引:31
作者
Chen, Jie [1 ]
Xia, Jun [1 ]
Yu, Yong-lin [1 ]
Wang, Si-qun [1 ]
Wei, Yi-bing [1 ]
Chen, Fei-yan [1 ]
Huang, Gang-yong [1 ]
Shi, Jing-sheng [1 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Orthoped, Shanghai 200040, Peoples R China
关键词
Osteosarcoma; Cell proliferation; HDAC5; Twist; 1; HISTONE DEACETYLASE INHIBITORS; TUMOR-CELL GROWTH; METASTASIS; DIFFERENTIATION; THERAPY;
D O I
10.1007/s13277-013-1189-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Histone deacetylases (HDACs) form a family of enzymes, which have fundamental roles in the epigenetic regulation of gene expression and contribute to the growth, differentiation, and apoptosis of cancer cells. In this study, we firstly investigated the biological function of HDAC5 in osteosarcoma cells. We found that mRNA and protein levels of HDAC5 were upregulated in osteosarcoma tissues and cell lines. Furthermore, overexpression of HDAC5 could promote cell proliferation in osteosarcoma cell lines. In contrast, HDAC5 knockdown using small interfering RNA inhibited cell proliferation. At the molecular level, we demonstrated that HDAC5 promoted mRNA expression of twist 1, which has been reported as an oncogene. Together, these results highlighted for the first time an unrecognized link between HDAC5 and osteosarcoma progression and demonstrated that its specific inhibition might contribute to the treatment of tumorigenesis.
引用
收藏
页码:1383 / 1387
页数:5
相关论文
共 24 条
[1]
Induction of EMT by twist proteins as a collateral effect of tumor-promoting inactivation of premature senescence [J].
Ansieau, Stephane ;
Bastid, Jeremy ;
Doreau, Agnes ;
Morel, Anne-Pierre ;
Bouchet, Benjamin P. ;
Thomas, Clemence ;
Fauvet, Frederique ;
Puisieux, Isabelle ;
Doglioni, Claudio ;
Piccinin, Sara ;
Maestro, Roberta ;
Voeltzel, Thibault ;
Selmi, Abdelkader ;
Valsesia-Wittmann, Sandrine ;
de Fromentel, Claude Caron ;
Puisieux, Alain .
CANCER CELL, 2008, 14 (01) :79-89
[2]
Anticancer activities of histone deacetylase inhibitors [J].
Bolden, Jessica E. ;
Peart, Melissa J. ;
Johnstone, Ricky W. .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (09) :769-784
[3]
Snail2 is an Essential Mediator of Twist1-Induced Epithelial Mesenchymal Transition and Metastasis [J].
Casas, Esmeralda ;
Kim, Jihoon ;
Bendesky, Andres ;
Ohno-Machado, Lucila ;
Wolfe, Cecily J. ;
Yang, Jing .
CANCER RESEARCH, 2011, 71 (01) :245-254
[4]
Von Willebrand factor expression in osteosarcoma metastasis [J].
Eppert, K ;
Wunder, JS ;
Aneliunas, V ;
Kandel, R ;
Andrulis, IL .
MODERN PATHOLOGY, 2005, 18 (03) :388-397
[5]
The many roles of histone deacetylases in development and physiology: implications for disease and therapy [J].
Haberland, Michael ;
Montgomery, Rusty L. ;
Olson, Eric N. .
NATURE REVIEWS GENETICS, 2009, 10 (01) :32-42
[6]
Kao HY, 2000, GENE DEV, V14, P55
[7]
HDAC inhibitors in cancer biology: emerging mechanisms and clinical applications [J].
Khan, Omar ;
La Thangue, Nicholas B. .
IMMUNOLOGY AND CELL BIOLOGY, 2012, 90 (01) :85-94
[8]
Osteosarcoma - Anatomic and histologic variants [J].
Klein, MJ ;
Siegal, GP .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2006, 125 (04) :555-581
[9]
Unraveling the hidden catalytic activity of vertebrate class Ila histone deacetylases [J].
Lahm, A. ;
Paolini, C. ;
Pallaoro, M. ;
Nardi, M. C. ;
Jones, P. ;
Neddermann, P. ;
Sambucini, S. ;
Bottomley, M. J. ;
Lo Surdo, P. ;
Carfi, A. ;
Koch, U. ;
De Francesco, R. ;
Steinkuehler, C. ;
Gallinari, P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (44) :17335-17340
[10]
Chromosomal organization and localization of the human histone deacetylase 5 gene (HDAC5) [J].
Mahlknecht, U ;
Schnittger, S ;
Ottmann, OG ;
Schoch, C ;
Mosebach, M ;
Hiddemann, W ;
Hoelzer, D .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2000, 1493 (03) :342-348