Copyright
©The Author(s) 2015.
World J Gastroenterol. Nov 14, 2015; 21(42): 12042-12058
Published online Nov 14, 2015. doi: 10.3748/wjg.v21.i42.12042
Published online Nov 14, 2015. doi: 10.3748/wjg.v21.i42.12042
Expression systems | Advantages | Disadvantages |
Constitutive | Well established, commercially available; in vitro and in vivo, successful methodology for expression of transgene | Expression of oncogenes may cause advanced/highly aggressive tumors and early lethality |
Heat-shock | Expression of transgene can be induced on a single cell level | Adverse effects that may arise from the heat shock |
Cre-loxP | Well established; commercially available; in vivo, successful methodology for expression of transgene | Not all tissue specific promoters are perfectly specific; leaky gene expression; two plasmid system |
GAL4/UAS | Well established; in vivo, successful methodology for expression of transgene | In vivo expression of GAL4 can have side effects, probably related to immune and stress responses; two plasmid system |
Mifepristone | Well established; in vivo, successful methodology for expression of transgene | Opening and closing of the switch is slow (hours to days); cell permeability of the RU-486 can be restricted |
Tet-on/off-inducible | Well established; commercially available; in vitro and in vivo, successful methodology for expression of transgene | Opening and closing of the switch is slow (hours to days); cell permeability of the doxycycline can be restricted; two plasmid system |
Nucleases | ZFN | TALEN | CRISPR/Cas |
DNA binding domain | Multiple zinc finger peptides | Transcription-activator like effectors | CRISPR-derived RNA/Single-guide RNA |
Endonuclease | Fok1 | Fok1 | Cas9 |
Binding specificity of each repeat | 3 bp | 2 bp | 1 bp |
Target site length | 18 to 36 bp | 30 to 40 bp | 23 bp |
Off-target | High probability | Low probability | Variable |
Libraries generation | No | Feasible, depend on technology | Yes, cloning 20 bp, oligos targeting each gene into a plasmid |
Transgene name | Expression system | Liver pathology | Ref. |
cnr1 (Zebrafish) | Tet-off-inducible | Steatosis | [132] |
edn1 (Zebrafish) | Constitutive | Steatosis, bile duct dilation, hyperplasia and HCC | [69] |
gankyrin (Zebrafish) | Constitutive | Atrophy, hypoplasia and steatosis | [123] |
HBx (Human) | Constitutive | Hypoplasia and steatosis | [120] |
HBx + AFB1 (Human) | Constitutive | Hepatitis, steatosis and hyperplasia | [134] |
HBx + HCV (Human) | Tet-off-inducible | Intrahepatic cholangiocarcinoma | [81] |
HBx + p53M214 (Human) | Constitutive | Chronic inflammation, steatosis, bile duct dilation, dysplasia and HCC | [70] |
HBx + src (Human/Zebrafish) | Constitutive | Chronic inflammation, steatosis, bile duct dilation, dysplasia and HCC | [70] |
HCV (Human) | Constitutive | Steatosis | [29] |
HCV + TAA (Human) | Constitutive | Steatosis and HCC | [29] |
kras-G12V (Zebrafish) | Mifepristone | Hyperplasia and HCC | [82] |
kras-G12V (Zebrafish) | Constitutive | Hyperplasia and hepatocellular adenoma | [82] |
kras-G12V (Zebrafish) | Tet-on-inducible | Hyperplasia, hepatocellular adenoma and HCC | [137] |
kras-G12V + p53M214 (Zebrafish) | Constitutive | Hyperplasia and hepatocellular adenoma | [82] |
kras-G12V + RhoA (Zebrafish) | Tet-on-inducible | Hyperplasia, hepatocellular adenoma and HCC | [137] |
kras-G12V + RhoAG14V (Zebrafish) | Tet-on-inducible | Hyperplasia, hepatocellular adenoma and HCC | [137] |
kras-G12V + RhoAT19N (Zebrafish) | Tet-on-inducible | HCC | [137] |
Lc3 (Rat) | Constitutive | Investigation of liver autophagy | [141] |
mdm2 (Zebrafish) | Constitutive | Atrophy, contraction and hypoplasia | [121] |
MYC (Mouse) | Tet-on-inducible | Hyperplasia and hepatocellular adenoma | [83] |
myca (Zebrafish) | Mifepristone | Small, typical, hypervascular and ascites of liver tumor | [143] |
myca + p53M214 (Zebrafish) | Mifepristone | Small, typical, hypervascular and ascites of liver tumor | [143] |
mycb (Zebrafish) | Mifepristone | Small, typical, hypervascular and ascites of liver tumor | [143] |
orf A (Human) | GAL4/UAS | Delayed onset of liver tumor | [79] |
src (Zebrafish) | Constitutive | Chronic inflammation, steatosis, bile duct dilation, hyperplasia, dysplasia and HCC | [70] |
src + p53M214 (Zebrafish) | Constitutive | Steatosis, hyperplasia, dysplasia and HCC | [70] |
UHRF1 (Human) | Constitutive | Atypical cells, dysplastic foci and HCC | [124] |
UHRF1 + p53M214 (Human) | Constitutive | Atypical cells, dysplastic foci and HCC | [124] |
xmrk (Xiphophorus) | Tet-on-inducible | Hyperplasia, hepatocellular adenoma and HCC | [80] |
yy1 (Zebrafish) | Constitutive | Steatosis | [131] |
zfBLP1 (Zebrafish) | Constitutive | Hyperplasia | [133] |
zfMcl-1α (Zebrafish) | Constitutive | Hyperplasia | [133] |
- Citation: Lu JW, Ho YJ, Yang YJ, Liao HA, Ciou SC, Lin LI, Ou DL. Zebrafish as a disease model for studying human hepatocellular carcinoma. World J Gastroenterol 2015; 21(42): 12042-12058
- URL: https://www.wjgnet.com/1007-9327/full/v21/i42/12042.htm
- DOI: https://dx.doi.org/10.3748/wjg.v21.i42.12042