2010
DOI: 10.1016/j.addr.2010.01.002
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Genetically modified cells in regenerative medicine and tissue engineering☆

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Cited by 71 publications
(40 citation statements)
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“…The current treatments are based on transplantation of autologous chondrocytes and osteochondral allografts (Bartlett et al 2005; Sheyn et al 2010; Augustyniak et al 2015). In this regard, pluripotent stem cells have arisen as an attractive cell source for repairing large cartilage defects after the primary surgery of the laryngeal cancer.…”
Section: Cartilagementioning
confidence: 99%
“…The current treatments are based on transplantation of autologous chondrocytes and osteochondral allografts (Bartlett et al 2005; Sheyn et al 2010; Augustyniak et al 2015). In this regard, pluripotent stem cells have arisen as an attractive cell source for repairing large cartilage defects after the primary surgery of the laryngeal cancer.…”
Section: Cartilagementioning
confidence: 99%
“…One possible route to overcome this issue is through the use of genetically engineered cell therapy, which has become a cutting-edge approach for tissue regeneration, and it has been under intensive experimental evaluation. 196,197 Cell-based gene delivery approaches to induce bone formation through the transfection of cells with BMP-2, 4, 6, 7, and 9 genes have led to superior bone formation in several animal models. [198][199][200][201][202][203] Gene therapy approaches for cartilage regeneration have also been explored with transfection of cells with BMP-2, BMP-7, TGF-b1, IGF-1, among others, acting individually or in synergy.…”
Section: From Single To Multiple Bioactive Factor Delivery For Skeletmentioning
confidence: 99%
“…Moreover, due to the extensive process of isolation of growth factors in their purified form for tissue development, subsequently increases its cost. Thus, genetic manipulations of cells to increase the expression of target gene for the high degree of function is becoming an important focus by researchers to establish genetically modified cells with overexpressed gene function for tissue regeneration [115]. For this purpose, the most common approach for enhancing electrostatic interactions between target cells and gene vectors is by means of cationic agents such as cationic liposomes [116,117] and polymers [118].…”
Section: Magnetofectionmentioning
confidence: 99%