Literature DB >> 24552821

Invading cancer cells are predominantly in G0/G1 resulting in chemoresistance demonstrated by real-time FUCCI imaging.

Shuya Yano1, Shinji Miwa2, Sumiyuki Mii2, Yukihiko Hiroshima2, Fuminari Uehara2, Mako Yamamoto2, Hiroyuki Kishimoto3, Hiroshi Tazawa4, Michael Bouvet5, Toshiyoshi Fujiwara3, Robert M Hoffman2.   

Abstract

Invasive cancer cells are a critical target in order to prevent metastasis. In the present report, we demonstrate real-time visualization of cell cycle kinetics of invading cancer cells in 3-dimensional (3D) Gelfoam® histoculture, which is in vivo-like. A fluorescence ubiquitination cell cycle indicator (FUCCI) whereby G0/G1 cells express a red fluorescent protein and S/G2/M cells express a green fluorescent protein was used to determine the cell cycle position of invading and non-invading cells. With FUCCI 3D confocal imaging, we observed that cancer cells in G0/G1 phase in Gelfoam® histoculture migrated more rapidly and further than cancer cells in S/G2/M phases. Cancer cells ceased migrating when they entered S/G2/M phases and restarted migrating after cell division when the cells re-entered G0/G1. Migrating cancer cells also were resistant to cytotoxic chemotherapy, since they were preponderantly in G0/G1, where cytotoxic chemotherapy is not effective. The results of the present report suggest that novel therapy targeting G0/G1 cancer cells should be developed to prevent metastasis.

Entities:  

Keywords:  3D; FUCCI; Gelfoam histoculture; cancer invasion; cell cycle kinetics; confocal laser microscopy; fluorescent proteins; real-time imaging

Mesh:

Substances:

Year:  2014        PMID: 24552821      PMCID: PMC3984318          DOI: 10.4161/cc.27818

Source DB:  PubMed          Journal:  Cell Cycle        ISSN: 1551-4005            Impact factor:   4.534


  24 in total

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  32 in total

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4.  Cancer cells mimic in vivo spatial-temporal cell-cycle phase distribution and chemosensitivity in 3-dimensional Gelfoam® histoculture but not 2-dimensional culture as visualized with real-time FUCCI imaging.

Authors:  Shuya Yano; Shinji Miwa; Sumiyuki Mii; Yukihiko Hiroshima; Fuminaru Uehara; Hiroyuki Kishimoto; Hiroshi Tazawa; Ming Zhao; Michael Bouvet; Toshiyoshi Fujiwara; Robert M Hoffman
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7.  Cell-cycle fate-monitoring distinguishes individual chemosensitive and chemoresistant cancer cells in drug-treated heterogeneous populations demonstrated by real-time FUCCI imaging.

Authors:  Shinji Miwa; Shuya Yano; Hiroaki Kimura; Mako Yamamoto; Makoto Toneri; Yasunori Matsumoto; Fuminari Uehara; Yukihiko Hiroshima; Takashi Murakami; Katsuhiro Hayashi; Norio Yamamoto; Michael Bouvet; Toshiyoshi Fujiwara; Hiroyuki Tsuchiya; Robert M Hoffman
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9.  Tumor-targeting Salmonella typhimurium A1-R decoys quiescent cancer cells to cycle as visualized by FUCCI imaging and become sensitive to chemotherapy.

Authors:  Shuya Yano; Yong Zhang; Ming Zhao; Yukihiko Hiroshima; Shinji Miwa; Fuminari Uehara; Hiroyuki Kishimoto; Hiroshi Tazawa; Michael Bouvet; Toshiyoshi Fujiwara; Robert M Hoffman
Journal:  Cell Cycle       Date:  2014       Impact factor: 4.534

10.  Invasive Cell Fate Requires G1 Cell-Cycle Arrest and Histone Deacetylase-Mediated Changes in Gene Expression.

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