Literature DB >> 14593724

From DNA damage to G2 arrest: the many roles of topoisomerase II.

Annette K Larsen1, Alexandre E Escargueil, Andrzej Skladanowski.   

Abstract

DNA topoisomerase II inhibitors are among the most widely used anticancer agents. These drugs are potent inducers of DNA strand breaks and G2 arrest. However, topoisomerase II is not only a target for anti-cancer drugs but also part of the cellular response to different types of DNA damage. Topoisomerase II forms molecular complexes with important cell cycle regulators including the p53 oncogene suppressor, the BRCT-containing protein TopBP1, 14-3-3 epsilon and Cdc2 kinase. The association between topoisomerase II and Cdc2 kinase likely represents the earliest step in mitotic chromatin condensation. Therefore, regulation of the topoisomerase II/Cdc2 interaction could represent a novel mechanism to delay mitotic onset.

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Year:  2003        PMID: 14593724

Source DB:  PubMed          Journal:  Prog Cell Cycle Res        ISSN: 1087-2957


  18 in total

1.  Mitosis-specific MPM-2 phosphorylation of DNA topoisomerase IIalpha is regulated directly by protein phosphatase 2A.

Authors:  Alexandre E Escargueil; Annette K Larsen
Journal:  Biochem J       Date:  2007-04-15       Impact factor: 3.857

2.  Type II topoisomerase activities in both the G1 and G2/M phases of the dinoflagellate cell cycle.

Authors:  Carmen K M Mak; Victor K L Hung; Joseph T Y Wong
Journal:  Chromosoma       Date:  2005-11-15       Impact factor: 4.316

3.  Evaluating the genotoxicity of topoisomerase-targeted antibiotics.

Authors:  Daniel J Smart; Anthony M Lynch
Journal:  Mutagenesis       Date:  2011-12-07       Impact factor: 3.000

4.  Induction of expression of a 14-3-3 gene in response to copper exposure in the marine alga, Fucus vesiculosus.

Authors:  Jennifer R Owen; Ceri A Morris; Beate Nicolaus; John L Harwood; Peter Kille
Journal:  Ecotoxicology       Date:  2011-09-11       Impact factor: 2.823

5.  Mitochondria are the primary target in the induction of apoptosis by chiral ruthenium(II) polypyridyl complexes in cancer cells.

Authors:  Jin-Quan Wang; Ping-Yu Zhang; Chen Qian; Xiao-Juan Hou; Liang-Nian Ji; Hui Chao
Journal:  J Biol Inorg Chem       Date:  2013-11-28       Impact factor: 3.358

6.  Protein kinase C β inhibition by enzastaurin leads to mitotic missegregation and preferential cytotoxicity toward colorectal cancer cells with chromosomal instability (CIN).

Authors:  Djamila Ouaret; Annette K Larsen
Journal:  Cell Cycle       Date:  2014       Impact factor: 4.534

7.  (-)-Xanthatin up-regulation of the GADD45γ tumor suppressor gene in MDA-MB-231 breast cancer cells: role of topoisomerase IIα inhibition and reactive oxygen species.

Authors:  Shuso Takeda; Momoko Noguchi; Kazumasa Matsuo; Yasuhiro Yamaguchi; Taichi Kudo; Hajime Nishimura; Yoshiko Okamoto; Toshiaki Amamoto; Mitsuru Shindo; Curtis J Omiecinski; Hironori Aramaki
Journal:  Toxicology       Date:  2013-01-08       Impact factor: 4.221

8.  Enhanced antitumor activity of combinations of free and HPMA copolymer-bound drugs.

Authors:  J Hongrapipat; P Kopecková; S Prakongpan; J Kopecek
Journal:  Int J Pharm       Date:  2007-09-22       Impact factor: 5.875

9.  Autoimmunity gene expression portrait: specific signature that intersects or differentiates between multiple sclerosis and systemic lupus erythematosus.

Authors:  M Mandel; M Gurevich; R Pauzner; N Kaminski; A Achiron
Journal:  Clin Exp Immunol       Date:  2004-10       Impact factor: 4.330

10.  Selective cytotoxic activity of the marine-derived batzelline compounds against pancreatic cancer cell lines.

Authors:  Esther A Guzmán; Jacob D Johnson; Megan K Carrier; Cara I Meyer; Tara P Pitts; Sarath P Gunasekera; Amy E Wright
Journal:  Anticancer Drugs       Date:  2009-02       Impact factor: 2.248

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