From: Cancer cell reprogramming: a promising therapy converting malignancy to benignity
Cancer type | Cell line | Reprogramming approach | Delivery method | Cell fate | Efficiency | Effects | Publication year | References |
---|---|---|---|---|---|---|---|---|
Melanoma | R545 | In vitro introduction of KLF4, Oct-3/4, c-Myc | Retrovirus | Pluripotent cancer cells | 0.05%–0.1% | Demethylation of the Oct-4 and NANOG promoter regions and loss of in vivo tumorigenicity in chimeras | 2009 | Utikal et al. [59] |
Pancreatic cancer | MIAPaCa-2 | In vitro introduction of KLF4, Oct-3/4, SOX2, c-Myc | Retrovirus and lentivirus | Pluripotent cancer cells | Not determined | Stable differentiation into varied lineages and loss of in vivo tumorigenicity in NOD/SCID mice | 2010 | Miyoshi et al. [60] |
Hepatocellular carcinoma | PLC | |||||||
Colorectal carcinoma | DLD-1, HCT116 | |||||||
B cell lymphoma and leukemia | RCH-ACV, CEMO-1, Val, MUTZ5, NALM-20 | In vitro introduction of C/EBPα | Retrovirus and lentivirus | Macrophage-like cells | 80% partially or entirely reprogrammed | Up-regulation of macrophage-associated markers and loss of in vivo tumorigenicity in immunodeficient mice | 2013 | Rapino et al. [70] |
Hepatocellular carcinoma | HCCLM3 and Huh7 | In vitro introduction of HNF1A, HNF4A, and FOXA3 | Adenovirus | Hepatocyte-like cells | 100% infection efficiency, reprogramming efficiency not determined | Recover of hepatocyte functions and capability of in vivo liver regeneration | 2018 | Cheng et al. [76] |
BCR-ABL1 + precursor B-cell acute lymphoblastic leukemia | Human B-ALL clinical samples | In vitro delivery of FLT3L, IL-7, IL-3, GM-CSF, MCSF | Culture medium | Macrophage-like cells | 53% initially reprogrammed; After sorting, > 98% yield | Recover of phagocytic ability and loss of in vivo tumorigenicity | 2015 | McClellan et al. [88] |
In vitro introduction of C/EBPα or PU.1 | Nucleofection | |||||||
Breast cancer | Py2T | In vitro delivery of TGF- β or Trametinib, in vivo EMT induction using Cre mice | Culture medium, animal model | Adipocytes | 60% reprogrammed | Recover of in vitro adipocyte functions and loss of in vivo metastatic potential | 2019 | Ishay-Ronen et al. [89] |
Skin cancer | Colo and PC3 | in vitro introduction of MicroRNA-302s | Retrovirus | Pluripotent embryonic stem-like cells | 100% transfection efficiency, 2%–5% reprogramming efficiency | Stable differentiation into varied lineages and loss of in vivo tumorigenicity | 2008 | Lin et al. [102] |
Breast cancer | MCF-7 and MDA-MB-231 | in vitro delivery human embryonic stem cells-derived exosomes | Culture medium | Pluripotent embryonic stem-like cells | 90% of breast cancer cells lost Vimentin expression | Recover of benign differentiation pathways and reduction of in vivo tumor-forming potential | 2017 | Zhou et al. [112] |
Colorectal carcinoma | Colo-320 and HT-29 |