| Literature DB >> 25483077 |
Shuya Yano1, Yong Zhang, Ming Zhao, Yukihiko Hiroshima, Shinji Miwa, Fuminari Uehara, Hiroyuki Kishimoto, Hiroshi Tazawa, Michael Bouvet, Toshiyoshi Fujiwara, Robert M Hoffman.
Abstract
Quiescent cancer cells are resistant to cytotoxic agents which target only proliferating cancer cells. Time-lapse imaging demonstrated that tumor-targeting Salmonella typhimurium A1-R (A1-R) decoyed cancer cells in monolayer culture and in tumor spheres to cycle from G0/G1 to S/G2/M, as demonstrated by fluorescence ubiquitination-based cell cycle indicator (FUCCI) imaging. A1-R infection of FUCCI-expressing subcutaneous tumors growing in nude mice also decoyed quiescent cancer cells, which were the majority of the cells in the tumors, to cycle from G0/G1 to S/G2/M, thereby making them sensitive to cytotoxic agents. The combination of A1-R and cisplatinum or paclitaxel reduced tumor size compared with A1-R monotherapy or cisplatinum or paclitaxel alone. The results of this study demonstrate that A1-R can decoy quiescent cancer cells to cycle to S/G2/M and sensitize them to cytotoxic chemotherapy. These results suggest a new paradigm of bacterial-decoy chemotherapy of cancer.Entities:
Keywords: FUCCI; GFP, RFP, imaging; S. typhimurium A1-R; Salmonella typhimurium; cell cycle; chemotherapy; decoy; fluorescence ubiquitination-based cell cycle indicator; S. typhimurium; tumor-targeting bacteria
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Year: 2014 PMID: 25483077 PMCID: PMC4615054 DOI: 10.4161/15384101.2014.964115
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534