Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/113527
Title: Inhibition of histone deacetylase 2 increases apoptosis and p21Cip1/WAF1 expression, independent of histone deacetylase 1
Authors: Huang, B.H.
Laban, M.
Leung, C.H.-W.
Lee, L.
Lee, C.K.
Salto-Tellez, M. 
Raju, G.C.
Hooi, S.C.
Keywords: Apoptosis
Cancer marker
Differentiation
Histone deacetylase
P21Cip1/WAF1
Tumorigenesis
Issue Date: Apr-2005
Citation: Huang, B.H., Laban, M., Leung, C.H.-W., Lee, L., Lee, C.K., Salto-Tellez, M., Raju, G.C., Hooi, S.C. (2005-04). Inhibition of histone deacetylase 2 increases apoptosis and p21Cip1/WAF1 expression, independent of histone deacetylase 1. Cell Death and Differentiation 12 (4) : 395-404. ScholarBank@NUS Repository.
Abstract: Histone deacetylases (HDACs) 1 and 2 share a high degree of homology and coexist within the same protein complexes. Despite their close association, each possesses unique functions. We show that the upregulation of HDAC2 in colorectal cancer occurred early at the polyp stage, was more robust and occurred more frequently than HDAC1. Similarly, while the expression of HDACs1 and 2 were increased in cervical dysplasia and invasive carcinoma, HDAC2 expression showed a clear demarcation of high-intensity staining at the transition region of dysplasia compared to HDAC1. Upon HDAC2 knockdown, cells displayed an increased number of cellular extensions reminiscent of cell differentiation. There was also an increase in apoptosis, associated with increased p21Cip1/WAF1 expression that was independent of p53. These results suggest that HDACs, especially HDAC2, are important enzymes involved in the early events of carcinogenesis, making them candidate markers for tumor progression and targets for cancer therapy. © 2005 Nature Publishing Group All rights reserved.
Source Title: Cell Death and Differentiation
URI: http://scholarbank.nus.edu.sg/handle/10635/113527
ISSN: 13509047
Appears in Collections:Staff Publications

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