Literature DB >> 30067968

Ki67 is a Graded Rather than a Binary Marker of Proliferation versus Quiescence.

Iain Miller1, Mingwei Min1, Chen Yang2, Chengzhe Tian1, Sara Gookin1, Dylan Carter1, Sabrina L Spencer3.   

Abstract

Ki67 staining is widely used as a proliferation indicator in the clinic, despite poor understanding of this protein's function or dynamics. Here, we track Ki67 levels under endogenous control in single cells over time and find that Ki67 accumulation occurs only during S, G2, and M phases. Ki67 is degraded continuously in G1 and G0 phases, regardless of the cause of entry into G0/quiescence. Consequently, the level of Ki67 during G0 and G1 in individual cells is highly heterogeneous and depends on how long an individual cell has spent in G0. Thus, Ki67 is a graded rather than a binary marker both for cell-cycle progression and time since entry into quiescence.
Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CDK2 activity; Ki67; heterogeneity; quiescence; single-cell tracking; time-lapse imaging

Mesh:

Substances:

Year:  2018        PMID: 30067968      PMCID: PMC6108547          DOI: 10.1016/j.celrep.2018.06.110

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  21 in total

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Authors:  Xiaoming Sun; Aizhan Bizhanova; Timothy D Matheson; Jun Yu; Lihua Julie Zhu; Paul D Kaufman
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3.  Dynamics of CDKN1A in Single Cells Defined by an Endogenous Fluorescent Tagging Toolkit.

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4.  Chromophore-assisted light inactivation of pKi-67 leads to inhibition of ribosomal RNA synthesis.

Authors:  R Rahmanzadeh; G Hüttmann; J Gerdes; T Scholzen
Journal:  Cell Prolif       Date:  2007-06       Impact factor: 6.831

Review 5.  The DREAM complex: master coordinator of cell cycle-dependent gene expression.

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Journal:  Nat Rev Cancer       Date:  2013-07-11       Impact factor: 60.716

6.  Cell-Cycle Regulation Accounts for Variability in Ki-67 Expression Levels.

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7.  Highly multiplexed imaging of single cells using a high-throughput cyclic immunofluorescence method.

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8.  Ki-67 is required for maintenance of cancer stem cells but not cell proliferation.

Authors:  Justin Cidado; Hong Yuen Wong; D Marc Rosen; Ashley Cimino-Mathews; Joseph P Garay; Abigail G Fessler; Zeshaan A Rasheed; Jessica Hicks; Rory L Cochran; Sarah Croessmann; Daniel J Zabransky; Morassa Mohseni; Julia A Beaver; David Chu; Karen Cravero; Eric S Christenson; Arielle Medford; Austin Mattox; Angelo M De Marzo; Pedram Argani; Ajay Chawla; Paula J Hurley; Josh Lauring; Ben Ho Park
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9.  The cell proliferation antigen Ki-67 organises heterochromatin.

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Journal:  Elife       Date:  2016-03-07       Impact factor: 8.140

10.  A map of protein dynamics during cell-cycle progression and cell-cycle exit.

Authors:  Sara Gookin; Mingwei Min; Harsha Phadke; Mingyu Chung; Justin Moser; Iain Miller; Dylan Carter; Sabrina L Spencer
Journal:  PLoS Biol       Date:  2017-09-11       Impact factor: 8.029

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  104 in total

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Journal:  J Thorac Cardiovasc Surg       Date:  2019-05-17       Impact factor: 5.209

2.  Pan-Cancer Survey of Tumor Mass Dormancy and Underlying Mutational Processes.

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3.  Cell Cycle Profiling Reveals Protein Oscillation, Phosphorylation, and Localization Dynamics.

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4.  A novel evaluation method for Ki-67 immunostaining in paraffin-embedded tissues.

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5.  RABL6A Is an Essential Driver of MPNSTs that Negatively Regulates the RB1 Pathway and Sensitizes Tumor Cells to CDK4/6 Inhibitors.

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Journal:  Clin Cancer Res       Date:  2020-02-21       Impact factor: 12.531

6.  Cell proliferation detected using [18F]FLT PET/CT as an early marker of abdominal aortic aneurysm.

Authors:  Richa Gandhi; Christopher Cawthorne; Lucinda J L Craggs; John D Wright; Juozas Domarkas; Ping He; Joanna Koch-Paszkowski; Michael Shires; Andrew F Scarsbrook; Stephen J Archibald; Charalampos Tsoumpas; Marc A Bailey
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7.  β2 Integrins differentially regulate γδ T cell subset thymic development and peripheral maintenance.

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Review 8.  Slow-cycling (dormant) cancer cells in therapy resistance, cancer relapse and metastasis.

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9.  Proper timing of a quiescence period in precursor prospermatogonia is required for stem cell pool establishment in the male germline.

Authors:  Guihua Du; Melissa J Oatley; Nathan C Law; Colton Robbins; Xin Wu; Jon M Oatley
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Authors:  Osama Garwain; Xiaoming Sun; Divya Ramalingam Iyer; Rui Li; Lihua Julie Zhu; Paul D Kaufman
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