| Literature DB >> 24811200 |
Shuya Yano1, Yong Zhang2, Shinji Miwa3, Yasunori Tome3, Yukihiko Hiroshima3, Fuminari Uehara3, Mako Yamamoto3, Atsushi Suetsugu3, Hiroyuki Kishimoto4, Hiroshi Tazawa5, Ming Zhao2, Michael Bouvet6, Toshiyoshi Fujiwara4, Robert M Hoffman3.
Abstract
The phase of the cell cycle can determine whether a cancer cell can respond to a given drug. We report here on the results of monitoring of real-time cell cycle dynamics of cancer cells throughout a live tumor intravitally using a fluorescence ubiquitination cell cycle indicator (FUCCI) before, during, and after chemotherapy. In nascent tumors in nude mice, approximately 30% of the cells in the center of the tumor are in G₀/G₁ and 70% in S/G₂/M. In contrast, approximately 90% of cancer cells in the center and 80% of total cells of an established tumor are in G₀/G₁ phase. Similarly, approximately 75% of cancer cells far from (> 100 µm) tumor blood vessels of an established tumor are in G₀/G₁. Longitudinal real-time imaging demonstrated that cytotoxic agents killed only proliferating cancer cells at the surface and, in contrast, had little effect on quiescent cancer cells, which are the vast majority of an established tumor. Moreover, resistant quiescent cancer cells restarted cycling after the cessation of chemotherapy. Our results suggest why most drugs currently in clinical use, which target cancer cells in S/G₂/M, are mostly ineffective on solid tumors. The results also suggest that drugs that target quiescent cancer cells are urgently needed.Entities:
Keywords: FUCCI; cell cycle; confocal laser microscopy; dormancy; drug resistance; fluorescent proteins; tumor; tumor blood vessels
Mesh:
Substances:
Year: 2014 PMID: 24811200 PMCID: PMC4111702 DOI: 10.4161/cc.29156
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534