Literature DB >> 16557283

Targeting polo-like kinase 1 for cancer therapy.

Klaus Strebhardt1, Axel Ullrich.   

Abstract

Human polo-like kinase 1 (PLK1) is essential during mitosis and in the maintenance of genomic stability. PLK1 is overexpressed in human tumours and has prognostic potential in cancer, indicating its involvement in carcinogenesis and its potential as a therapeutic target. The use of different PLK1 inhibitors has increased our knowledge of mitotic regulation and allowed us to assess their ability to suppress tumour growth in vivo. We address the structural features of the kinase domain and the unique polo-box domain of PLK1 that are most suited for drug development and discuss our current understanding of the therapeutic potential of PLK1.

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Year:  2006        PMID: 16557283     DOI: 10.1038/nrc1841

Source DB:  PubMed          Journal:  Nat Rev Cancer        ISSN: 1474-175X            Impact factor:   60.716


  302 in total

Review 1.  Functions and regulation of the Polo-like kinase Cdc5 in the absence and presence of DNA damage.

Authors:  Vladimir V Botchkarev; James E Haber
Journal:  Curr Genet       Date:  2017-08-02       Impact factor: 3.886

2.  Plk1-mediated phosphorylation of UAP56 regulates the stability of UAP56.

Authors:  Fuyin Xiong; Yanli Lin; Zhengbin Han; Gengshou Shi; Liyuan Tian; Xiaojie Wu; Qiangcheng Zeng; Yanrong Zhou; Jixian Deng; Hongxing Chen
Journal:  Mol Biol Rep       Date:  2011-06-03       Impact factor: 2.316

3.  Identification of a novel Wnt5a-CK1ɛ-Dvl2-Plk1-mediated primary cilia disassembly pathway.

Authors:  Kyung Ho Lee; Yoshikazu Johmura; Li-Rong Yu; Jung-Eun Park; Yuan Gao; Jeong K Bang; Ming Zhou; Timothy D Veenstra; Bo Yeon Kim; Kyung S Lee
Journal:  EMBO J       Date:  2012-05-18       Impact factor: 11.598

Review 4.  Understanding cytokinesis failure.

Authors:  Guillaume Normand; Randall W King
Journal:  Adv Exp Med Biol       Date:  2010       Impact factor: 2.622

5.  Investigation of unanticipated alkylation at the N(π) position of a histidyl residue under Mitsunobu conditions and synthesis of orthogonally protected histidine analogues.

Authors:  Wenjian Qian; Fa Liu; Terrence R Burke
Journal:  J Org Chem       Date:  2011-10-03       Impact factor: 4.354

6.  Polo-box domain inhibitor poloxin activates the spindle assembly checkpoint and inhibits tumor growth in vivo.

Authors:  Juping Yuan; Mourad Sanhaji; Andrea Krämer; Wolfgang Reindl; Matthias Hofmann; Nina-Naomi Kreis; Brigitte Zimmer; Thorsten Berg; Klaus Strebhardt
Journal:  Am J Pathol       Date:  2011-08-10       Impact factor: 4.307

7.  PLK1 phosphorylates mitotic centromere-associated kinesin and promotes its depolymerase activity.

Authors:  Liangyu Zhang; Hengyi Shao; Yuejia Huang; Feng Yan; Youjun Chu; Hai Hou; Mei Zhu; Chuanhai Fu; Felix Aikhionbare; Guowei Fang; Xia Ding; Xuebiao Yao
Journal:  J Biol Chem       Date:  2010-11-15       Impact factor: 5.157

Review 8.  Cell cycle, CDKs and cancer: a changing paradigm.

Authors:  Marcos Malumbres; Mariano Barbacid
Journal:  Nat Rev Cancer       Date:  2009-03       Impact factor: 60.716

9.  Targeting PLK1 overcomes T-DM1 resistance via CDK1-dependent phosphorylation and inactivation of Bcl-2/xL in HER2-positive breast cancer.

Authors:  Özge Saatci; Simone Borgoni; Özge Akbulut; Selvi Durmuş; Umar Raza; Erol Eyüpoğlu; Can Alkan; Aytekin Akyol; Özgür Kütük; Stefan Wiemann; Özgür Şahin
Journal:  Oncogene       Date:  2018-02-02       Impact factor: 9.867

10.  RNAi screen identifies a synthetic lethal interaction between PIM1 overexpression and PLK1 inhibition.

Authors:  Riet van der Meer; Ha Yong Song; Seong-Hoon Park; Sarki A Abdulkadir; Meejeon Roh
Journal:  Clin Cancer Res       Date:  2014-04-25       Impact factor: 12.531

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