Results 31 to 40 of about 4,153 (193)

Consequences of Plk4 overexpression in mouse pancreatic organoids

open access: yes, 2021
Overexpression of the polo-like kinase 4 (Plk4), the master regulator of centrosome duplication, leads to centrosome amplification, a common feature of cancer, including pancreatic cancer. Previous studies have shown that overexpression of Plk4 in mice carrying a doxycycline-inducible Plk4 transgene (Plk4OE) causes centrosome amplification, a reduction
openaire   +3 more sources

The Polo kinase Plk4 functions in centriole duplication

open access: yesNature Cell Biology, 2005
The human Polo-like kinase 1 (PLK1) and its functional homologues that are present in other eukaryotes have multiple, crucial roles in meiotic and mitotic cell division. By contrast, the functions of other mammalian Polo family members remain largely unknown.
Habedanck, Robert   +3 more
openaire   +4 more sources

Plk4 Phosphorylates Ana2 to Trigger Sas6 Recruitment and Procentriole Formation [PDF]

open access: yesCurrent Biology, 2014
Centrioles are 9-fold symmetrical structures at the core of centrosomes and base of cilia whose dysfunction has been linked to a wide range of inherited diseases and cancer. Their duplication is regulated by a protein kinase of conserved structure, the C. elegans ZYG-1 or its Polo-like kinase 4 (Plk4) counterpart in other organisms.
Dzhindzhev N. S.   +8 more
openaire   +5 more sources

Polo-like kinase 4 as a potential predictive biomarker of chemoradioresistance in locally advanced rectal cancer [PDF]

open access: yesJournal of Pathology and Translational Medicine, 2022
Background Polo-like kinase 4 (PLK4) is a serine/threonine protein kinase located in the centriole of the chromosome during the cell cycle. PLK4 overexpression has been described in a variety of many common human epithelial tumors.
Hyunseung Oh   +8 more
doaj   +1 more source

Sak/Plk4 and mitotic fidelity [PDF]

open access: yesOncogene, 2005
Sak/Plk4 differs from other polo-like kinases in having only a single polo box, which assumes a novel dimer fold that localizes to the nucleolus, centrosomes and the cleavage furrow. Sak expression increases gradually in S through M phase, and Sak is destroyed by APC/C dependent proteolysis.
Carol J, Swallow   +4 more
openaire   +2 more sources

Fast and furious . . . or not, Plk4 dictates the pace [PDF]

open access: yesJournal of Cell Biology, 2018
In each duplication cycle, daughter centrioles grow to the same length as their mothers. Which mechanisms regulate this fidelity to maintain centriole length is not known. In this issue, Aydogan et al. (2018. J. Cell Biol. https://doi.org/10.1083/jcb.201801014) report a novel role for Polo-like kinase 4 (Plk4).
Gemble, Simon, Basto, Renata
openaire   +2 more sources

Use of the Polo-like kinase 4 (PLK4) inhibitor centrinone to investigate intracellular signalling networks using SILAC-based phosphoproteomics [PDF]

open access: yes, 2020
Polo-like kinase 4 (PLK4) is the master regulator of centriole duplication in metazoan organisms. Catalytic activity and protein turnover of PLK4 are tightly coupled in human cells, since changes in PLK4 concentration and catalysis have profound effects ...
Jones, Andrew R   +9 more
core   +1 more source

Down‐regulation of Polo‐like kinase 4 (PLK4) induces G1 arrest via activation of the p38/p53/p21 signaling pathway in bladder cancer

open access: yesFEBS Open Bio, 2021
Polo‐like kinase 4 (PLK4) has been reported to contribute to tumor growth, invasion, and metastasis. However, the role of PLK4 in human bladder cancer (BC) remains unclear.
Ziyi Yang   +6 more
doaj   +1 more source

Inhibition of Polo-like kinase 4 induces mitotic defects and DNA damage in diffuse large B-cell lymphoma

open access: yesCell Death and Disease, 2021
Polo-like kinase 4 (PLK4), a key regulator of centriole biogenesis, has recently been shown to play key roles in tumorigenesis. Blocking PLK4 expression by interference or targeted drugs exhibits attractive potential in improving the efficacy of ...
Yi Zhao   +8 more
doaj   +1 more source

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