| Literature DB >> 27715464 |
Shuya Yano1,2,3, Kiyoto Takehara1,2,3, Hiroshi Tazawa4, Hiroyuki Kishimoto3, Yasuo Urata5, Shunsuke Kagawa3, Toshiyoshi Fujiwara3, Robert M Hoffman1,2.
Abstract
We previously demonstrated that quiescent cancer cells in a tumor are resistant to conventional chemotherapy as visualized with a fluorescence ubiquitination cell cycle indicator (FUCCI). We also showed that proliferating cancer cells exist in a tumor only near nascent vessels or on the tumor surface as visualized with FUCCI and green fluorescent protein (GFP)-expressing tumor vessels. In the present study, we show the relationship between cell-cycle phase and chemotherapy-induced tumor angiogenesis using in vivo FUCCI real-time imaging of the cell cycle and nestin-driven GFP to detect nascent blood vessels. We observed that chemotherapy-treated tumors, consisting of mostly of quiescent cancer cells after treatment, had much more and deeper tumor vessels than untreated tumors. These newly-vascularized cancer cells regrew rapidly after chemotherapy. In contrast, formerly quiescent cancer cells decoyed to S/G2 phase by a telomerase-dependent adenovirus did not induce tumor angiogenesis. The present results further demonstrate the importance of the cancer-cell position in the cell cycle in order that chemotherapy be effective and not have the opposite effect of stimulating tumor angiogenesis and progression.Entities:
Keywords: FUCCI; angiogenesis; cell cycle; chemotherapy; decoy; imaging; quiescence; resistance
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Year: 2016 PMID: 27715464 PMCID: PMC5351920 DOI: 10.1080/15384101.2016.1220461
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534