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1
Plk5, a polo box domain-only protein with specific roles in neuron differentiation and glioblastoma suppression.Plk5,一种具有特定神经元分化和神经胶质瘤抑制作用的 polo 盒结构域蛋白。
Mol Cell Biol. 2011 Mar;31(6):1225-39. doi: 10.1128/MCB.00607-10. Epub 2011 Jan 18.
2
From Plk1 to Plk5: functional evolution of polo-like kinases.从 Plk1 到 Plk5: Polo 样激酶的功能进化。
Cell Cycle. 2011 Jul 15;10(14):2255-62. doi: 10.4161/cc.10.14.16494.
3
Non-mitotic functions of polo-like kinases in cancer cells.癌细 胞中类 极光激酶的非有丝分裂功能。
Biochim Biophys Acta Rev Cancer. 2021 Jan;1875(1):188467. doi: 10.1016/j.bbcan.2020.188467. Epub 2020 Nov 7.
4
The novel mouse Polo-like kinase 5 responds to DNA damage and localizes in the nucleolus.新型鼠类 Polo 样激酶 5 可响应 DNA 损伤,并定位于核仁。
Nucleic Acids Res. 2010 May;38(9):2931-43. doi: 10.1093/nar/gkq011. Epub 2010 Jan 25.
5
Potential Tumor Suppressor Role of Polo-like Kinase 5 in Cancer.Polo样激酶5在癌症中的潜在肿瘤抑制作用。
Cancers (Basel). 2023 Nov 17;15(22):5457. doi: 10.3390/cancers15225457.
6
Selective blockade of cancer cell proliferation and anchorage-independent growth by Plk1 activity-dependent suicidal inhibition of its polo-box domain.通过对其polo盒结构域的Plk1活性依赖性自杀抑制来选择性阻断癌细胞增殖和不依赖贴壁生长。
Cell Cycle. 2015;14(22):3624-34. doi: 10.1080/15384101.2015.1104435.
7
A potential tumor suppressor role of PLK2 in glioblastoma.PLK2在胶质母细胞瘤中的潜在肿瘤抑制作用。
FEBS Open Bio. 2025 May;15(5):856-866. doi: 10.1002/2211-5463.70000. Epub 2025 Feb 10.
8
Histone methyltransferase WHSC1 cooperate with YBX1 promote glioblastoma progression via regulating PLK1 expression.组蛋白甲基转移酶 WHSC1 与 YBX1 合作通过调节 PLK1 表达促进胶质母细胞瘤进展。
Cell Signal. 2024 Dec;124:111471. doi: 10.1016/j.cellsig.2024.111471. Epub 2024 Oct 13.
9
A high-content small molecule screen identifies sensitivity of glioblastoma stem cells to inhibition of polo-like kinase 1.一项高内涵小分子筛选确定了胶质母细胞瘤干细胞对抑制polo样激酶1的敏感性。
PLoS One. 2013 Oct 30;8(10):e77053. doi: 10.1371/journal.pone.0077053. eCollection 2013.
10
Polo-like kinase 1 inhibition causes decreased proliferation by cell cycle arrest, leading to cell death in glioblastoma.Polo-like kinase 1 抑制通过细胞周期阻滞导致增殖减少,从而导致胶质母细胞瘤细胞死亡。
Cancer Gene Ther. 2013 Sep;20(9):499-506. doi: 10.1038/cgt.2013.46. Epub 2013 Jul 26.

引用本文的文献

1
More than 2,500 coding genes in the human reference gene set still have unsettled status.人类参考基因集中超过2500个编码基因的状态仍未确定。
bioRxiv. 2024 Dec 9:2024.12.05.626965. doi: 10.1101/2024.12.05.626965.
2
Application of a Fluorescence Recovery-Based Polo-Like Kinase 1 Binding Assay to Polo-Like Kinase 2 and Polo-Like Kinase 3.基于荧光恢复的 Polo 样激酶 1 结合分析法在 Polo 样激酶 2 和 Polo 样激酶 3 中的应用。
Biol Pharm Bull. 2024;47(7):1282-1287. doi: 10.1248/bpb.b24-00189.
3
Potential Tumor Suppressor Role of Polo-like Kinase 5 in Cancer.Polo样激酶5在癌症中的潜在肿瘤抑制作用。
Cancers (Basel). 2023 Nov 17;15(22):5457. doi: 10.3390/cancers15225457.
4
PLK3 facilitates replication of swine influenza virus by phosphorylating viral NP protein.PLK3 通过磷酸化病毒 NP 蛋白促进猪流感病毒的复制。
Emerg Microbes Infect. 2023 Dec;12(2):2275606. doi: 10.1080/22221751.2023.2275606. Epub 2023 Nov 15.
5
Comprehensive Characterization of Immune Cell Infiltration Characteristics and Drug Sensitivity Analysis in Inflammatory Breast Cancer Based on Bioinformatic Strategy.基于生物信息学策略的炎性乳腺癌免疫浸润特征的全面描述及药物敏感性分析。
Biochem Genet. 2024 Apr;62(2):1021-1039. doi: 10.1007/s10528-023-10460-3. Epub 2023 Jul 30.
6
Predicting late-stage age-related macular degeneration by integrating marginally weak SNPs in GWA studies.通过整合全基因组关联研究中微弱关联的单核苷酸多态性预测晚期年龄相关性黄斑变性
Front Genet. 2023 Mar 30;14:1075824. doi: 10.3389/fgene.2023.1075824. eCollection 2023.
7
Polo-like kinase (PLK) 5, a new member of the PLK family, serves as a biomarker to indicate anabatic tumor burden and poor prognosis for resectable non-small cell lung cancer.Polo样激酶(PLK)5是PLK家族的新成员,作为一种生物标志物,提示可切除的非小细胞肺癌患者肿瘤进展及预后不良。
Front Surg. 2023 Jan 6;9:964044. doi: 10.3389/fsurg.2022.964044. eCollection 2022.
8
Moonlighting at the Poles: Non-Canonical Functions of Centrosomes.两极的兼职:中心体的非经典功能
Front Cell Dev Biol. 2022 Jul 14;10:930355. doi: 10.3389/fcell.2022.930355. eCollection 2022.
9
Recent Progress on the Localization of PLK1 to the Kinetochore and Its Role in Mitosis.PLK1 在着丝粒上的定位及其在有丝分裂中的作用的最新进展。
Int J Mol Sci. 2022 May 8;23(9):5252. doi: 10.3390/ijms23095252.
10
Polo-like kinases as potential targets and PLK2 as a novel biomarker for the prognosis of human glioblastoma.Polo-like kinases 作为潜在靶点和 PLK2 作为人类神经胶质瘤预后的新型生物标志物。
Aging (Albany NY). 2022 Mar 7;14(5):2320-2334. doi: 10.18632/aging.203940.

本文引用的文献

1
Shared and separate functions of polo-like kinases and aurora kinases in cancer.Polo-like 激酶和 Aurora 激酶在癌症中的共同和独立功能。
Nat Rev Cancer. 2010 Dec;10(12):825-41. doi: 10.1038/nrc2964. Epub 2010 Nov 24.
2
Oncogenic and tumor suppressive roles of polo-like kinases in human hepatocellular carcinoma.Polo-like kinases 在人肝细胞癌中的致癌和抑癌作用。
Hepatology. 2010 Mar;51(3):857-68. doi: 10.1002/hep.23467.
3
The novel mouse Polo-like kinase 5 responds to DNA damage and localizes in the nucleolus.新型鼠类 Polo 样激酶 5 可响应 DNA 损伤,并定位于核仁。
Nucleic Acids Res. 2010 May;38(9):2931-43. doi: 10.1093/nar/gkq011. Epub 2010 Jan 25.
4
Polo-like kinases: conservation and divergence in their functions and regulation.Polo样激酶:其功能与调控的保守性与差异性
Nat Rev Mol Cell Biol. 2009 Apr;10(4):265-75. doi: 10.1038/nrm2653.
5
Structure of the pseudokinase VRK3 reveals a degraded catalytic site, a highly conserved kinase fold, and a putative regulatory binding site.假激酶VRK3的结构揭示了一个退化的催化位点、一个高度保守的激酶折叠以及一个假定的调节结合位点。
Structure. 2009 Jan 14;17(1):128-38. doi: 10.1016/j.str.2008.10.018.
6
Plk3 interacts with and specifically phosphorylates VRK1 in Ser342, a downstream target in a pathway that induces Golgi fragmentation.Plk3与VRK1相互作用,并特异性地在Ser342位点磷酸化VRK1,Ser342是诱导高尔基体碎片化途径中的一个下游靶点。
Mol Cell Biol. 2009 Mar;29(5):1189-201. doi: 10.1128/MCB.01341-08. Epub 2008 Dec 22.
7
Polo-like kinase 2 (PLK2) phosphorylates alpha-synuclein at serine 129 in central nervous system.Polo样激酶2(PLK2)在中枢神经系统中使α-突触核蛋白的丝氨酸129位点发生磷酸化。
J Biol Chem. 2009 Jan 30;284(5):2598-2602. doi: 10.1074/jbc.C800206200. Epub 2008 Nov 12.
8
Plk2 regulated centriole duplication is dependent on its localization to the centrioles and a functional polo-box domain.Plk2调控的中心粒复制依赖于其定位于中心粒以及一个功能性的Polo框结构域。
Cell Cycle. 2008 Nov 15;7(22):3548-55. doi: 10.4161/cc.7.22.7071. Epub 2008 Nov 26.
9
Polo-like kinase 1 reaches beyond mitosis--cytokinesis, DNA damage response, and development.Polo样激酶1的作用超出有丝分裂范畴——涉及胞质分裂、DNA损伤反应及发育过程。
Curr Opin Cell Biol. 2008 Dec;20(6):650-60. doi: 10.1016/j.ceb.2008.10.005. Epub 2008 Nov 27.
10
Regulation of postsynaptic RapGAP SPAR by Polo-like kinase 2 and the SCFbeta-TRCP ubiquitin ligase in hippocampal neurons.海马神经元中Polo样激酶2和SCFβ-TRCP泛素连接酶对突触后RapGAP SPAR的调控
J Biol Chem. 2008 Oct 24;283(43):29424-32. doi: 10.1074/jbc.M802475200. Epub 2008 Aug 22.

Plk5,一种具有特定神经元分化和神经胶质瘤抑制作用的 polo 盒结构域蛋白。

Plk5, a polo box domain-only protein with specific roles in neuron differentiation and glioblastoma suppression.

机构信息

Centro Nacional de Investigaciones Oncológicas, Melchor Fernández Almagro 3, E-28029 Madrid, Spain.

出版信息

Mol Cell Biol. 2011 Mar;31(6):1225-39. doi: 10.1128/MCB.00607-10. Epub 2011 Jan 18.

DOI:10.1128/MCB.00607-10
PMID:21245385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3067912/
Abstract

Polo-like kinases (Plks) are characterized by the presence of a specific domain, known as the polo box (PBD), involved in protein-protein interactions. Plk1 to Plk4 are involved in centrosome biology as well as the regulation of mitosis, cytokinesis, and cell cycle checkpoints in response to genotoxic stress. We have analyzed here the new member of the vertebrate family, Plk5, a protein that lacks the kinase domain in humans. Plk5 does not seem to have a role in cell cycle progression; in fact, it is downregulated in proliferating cells and accumulates in quiescent cells. This protein is mostly expressed in the brain of both mice and humans, and it modulates the formation of neuritic processes upon stimulation of the brain-derived neurotrophic factor (BDNF)/nerve growth factor (NGF)-Ras pathway in neurons. The human PLK5 gene is significantly silenced in astrocytoma and glioblastoma multiforme by promoter hypermethylation, suggesting a tumor suppressor function for this gene. Indeed, overexpression of Plk5 has potent apoptotic effects in these tumor cells. Thus, Plk5 seems to have evolved as a kinase-deficient PBD-containing protein with nervous system-specific functions and tumor suppressor activity in brain cancer.

摘要

丝氨酸/苏氨酸激酶(Polo-like kinases,Plks)的特征是存在一个特定的结构域,称为 Polo 盒(PBD),参与蛋白质-蛋白质相互作用。Plk1 到 Plk4 参与中心体生物学以及有丝分裂、胞质分裂和细胞周期检查点的调控,以应对遗传毒性应激。我们在这里分析了脊椎动物家族的新成员 Plk5,这是一种在人类中缺乏激酶结构域的蛋白质。Plk5 似乎在细胞周期进展中没有作用;事实上,它在增殖细胞中下调,并在静止细胞中积累。这种蛋白质主要在人和老鼠的大脑中表达,并在神经元中刺激脑源性神经营养因子(BDNF)/神经生长因子(NGF)-Ras 途径时调节神经突过程的形成。人类 PLK5 基因由于启动子超甲基化而在星形细胞瘤和多形性成胶质细胞瘤中显著沉默,表明该基因具有肿瘤抑制功能。事实上,Plk5 的过表达在这些肿瘤细胞中具有很强的凋亡作用。因此,Plk5 似乎已经进化为一种具有神经系统特异性功能和脑癌中肿瘤抑制活性的激酶缺失 PBD 蛋白。