| Literature DB >> 28246701 |
Ho-Chang Jeong1, Seung-Ju Cho1, Mi-Ok Lee2, Hyuk-Jin Cha3.
Abstract
Despite the recent promising results of clinical trials using human pluripotent stem cell (hPSC)-based cell therapies for age-related macular degeneration (AMD), the risk of teratoma formation resulting from residual undifferentiated hPSCs remains a serious and critical hurdle for broader clinical implementation. To mitigate the tumorigenic risk of hPSC-based cell therapy, a variety of approaches have been examined to ablate the undifferentiated hPSCs based on the unique molecular properties of hPSCs. In the present review, we offer a brief overview of recent attempts at selective elimination of undifferentiated hPSCs to decrease the risk of teratoma formation in hPSC-based cell therapy.Entities:
Keywords: Apoptosis; Human pluripotent stem cells; Safe stem cell therapy; Selective cell death; Teratoma
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Year: 2017 PMID: 28246701 DOI: 10.1007/s00018-017-2486-0
Source DB: PubMed Journal: Cell Mol Life Sci ISSN: 1420-682X Impact factor: 9.261