Literature DB >> 23325510

Cancers with wrong HATs: the impact of acetylation.

Vincenzo Di Cerbo1, Robert Schneider.   

Abstract

Lysine N-ε-acetylation is a post-translational modification that regulates the function of histone and non-histone proteins. In several malignancies, histone acetyltransferase (HAT) activities are disturbed as a consequence of various genetic or epigenetic alterations. In particular, HATs can function as tumor suppressors, helping cells control cellular proliferation and cell cycle, and also as oncogenes, because abnormal acetylation can activate malignant proteins and contribute to cancer. An impaired acetylation profile can be indicative of a pathological process, and thus evaluation of histone acetylation could be used as a predictive index of patient survival or therapy outcome. Therefore, epigenetic therapy might be a very effective strategy to defeat cancer. With the use of histone deacetylase inhibitors and acetylation modulators (e.g. HAT inhibitors, bromodomain inhibitors), we are paving the way for a future epigenetic drug control of human diseases.

Entities:  

Keywords:  acetylation; cancer; epigenetics; histone acetyltransferases; histone modifications

Mesh:

Substances:

Year:  2013        PMID: 23325510     DOI: 10.1093/bfgp/els065

Source DB:  PubMed          Journal:  Brief Funct Genomics        ISSN: 2041-2649            Impact factor:   4.241


  41 in total

Review 1.  Preserving genome integrity and function: the DNA damage response and histone modifications.

Authors:  Jae Jin Kim; Seo Yun Lee; Kyle M Miller
Journal:  Crit Rev Biochem Mol Biol       Date:  2019-06-04       Impact factor: 8.250

Review 2.  The emerging role of PI3K/AKT-mediated epigenetic regulation in cancer.

Authors:  Jennifer M Spangle; Thomas M Roberts; Jean J Zhao
Journal:  Biochim Biophys Acta Rev Cancer       Date:  2017-03-14       Impact factor: 10.680

3.  A time-series analysis of altered histone H3 acetylation and gene expression during the course of MMAIII-induced malignant transformation of urinary bladder cells.

Authors:  Jinqiu Zhu; Jie Wang; Xushen Chen; Maria Tsompana; Daniel Gaile; Michael Buck; Xuefeng Ren
Journal:  Carcinogenesis       Date:  2017-04-01       Impact factor: 4.944

4.  A quantitative multiplexed mass spectrometry assay for studying the kinetic of residue-specific histone acetylation.

Authors:  Yin-Ming Kuo; Ryan A Henry; Andrew J Andrews
Journal:  Methods       Date:  2014-08-11       Impact factor: 3.608

5.  Multigene signature for predicting prognosis of patients with 1p19q co-deletion diffuse glioma.

Authors:  Xin Hu; Emmanuel Martinez-Ledesma; Siyuan Zheng; Hoon Kim; Floris Barthel; Tao Jiang; Kenneth R Hess; Roel G W Verhaak
Journal:  Neuro Oncol       Date:  2017-06-01       Impact factor: 12.300

6.  The many metabolic sources of acetyl-CoA to support histone acetylation and influence cancer progression.

Authors:  Olivier Feron
Journal:  Ann Transl Med       Date:  2019-12

Review 7.  Targeting epigenetic regulators for cancer therapy: mechanisms and advances in clinical trials.

Authors:  Yuan Cheng; Cai He; Manni Wang; Xuelei Ma; Fei Mo; Shengyong Yang; Junhong Han; Xiawei Wei
Journal:  Signal Transduct Target Ther       Date:  2019-12-17

Review 8.  Epigenetic regulation of RTK signaling.

Authors:  Jennifer M Spangle; Thomas M Roberts
Journal:  J Mol Med (Berl)       Date:  2017-06-06       Impact factor: 4.599

Review 9.  Histone Modifications and Cancer.

Authors:  James E Audia; Robert M Campbell
Journal:  Cold Spring Harb Perspect Biol       Date:  2016-04-01       Impact factor: 10.005

10.  CDKN1A histone acetylation and gene expression relationship in gastric adenocarcinomas.

Authors:  Fernanda Wisnieski; Danielle Queiroz Calcagno; Mariana Ferreira Leal; Leonardo Caires Santos; Carolina Oliveira Gigek; Elizabeth Suchi Chen; Sâmia Demachki; Ricardo Artigiani; Paulo Pimentel Assumpção; Laércio Gomes Lourenço; Rommel Rodríguez Burbano; Marília Cardoso Smith
Journal:  Clin Exp Med       Date:  2015-11-14       Impact factor: 3.984

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.