From: Influencing factors and mechanism of hepatocyte regeneration
Literature | Time | Result | |
---|---|---|---|
[75] | 1982.11 | Int1 | Int1 gene was cloned from mouse breast cancer cells, and it was found that Int1 could promote the development of cancer. |
[76] | 1987.08 | Dint-1 | Dint-1, a homologue of int-1, was isolated from Drosophila melanogaster by cross hybridization. And Dint-1/wingless plays an important role as a signal of intercellular communication. |
[77] | 1989.06 | catenin | The catenin α, β and γ are named. |
[78] | 1991.11 | β- catenin | β -catenin was found in all the embryonic stages of Xenopus laevis, and was related to C- cadherin. |
[79] | 1996.05 | GSK3β | GSK3β can bind to β -catenin and Drosophila adenomatous polyposis coli gene (APC). |
[80] | 1996.08 | TCF-1/Lef-1 | TCF-1/Lef-1 can bind to β -catenin and can bind to target DNA as a complex. |
[81] | 1997.02 | Frizzled | The curled protein was identified as Wnt receptor and the function of Dishevelled was discussed. |
[82] | 1998.06 | GBP | GBP (a parent Xgsk-3 binding protein) inhibits the phosphorylation of Xgsk-3 in vivo and is an inhibitor of GSK-3. |
[83] | 1998.07 | Dsh | Dsh activates JNK pathway; Wnt/Frizzled signaling pathway uses multiple intracellular signal cascades. |
[84] | 1998.1 | TCF | CBP inhibits TCF. |
[85] | 1999.03 | Axin | Axin protein family is very important in Wnt/Wingless signal of Drosophila. |
[86] | 2000.09 | LRP6 | LRP6 plays a wide role in the transduction of several Wnt signals in mammals. |
[87] | 2002.05 | Wnt/Ca2+ | Wnt/Ca2 + pathway activates NF-AT and mediates ventral signals of Xenopus laevis embryos. |
[88] | 2002.04 | Notch | Wnt and Notch cascade |
[89] | 2002.04 | Hedgehog | Shaggy/GSK3 is also a negative regulator in Hedgehog (Hh) pathway. |
[90] | 2005.09 | c-Jun、 TCF4 | Phosphorylation-dependent interaction between c-Jun and TCF4 regulates intestinal tumorigenesis by integrating JNK and APC/β-catenin. |
[91] | 2007.05 | WTX | WTX promotes ubiquitination and degradation of β-catenin, thus antagonizing Wnt/β- catenin signal transduction. |
[92] | 2009.12 | Wnt | The axial mode of Wnt signal transduction is earlier than the evolution of bilaterally symmetrical animals. |
[93] | 2012.12 | TAZ | A large part of Wnt transcription reaction is mediated by TAZ. |
[94] | 2013.01 | YAP | YAP inhibits Wnt signal by limiting DVL nuclear translocation during regenerative growth. |
[95] | 2014.07 | YAP/TAZ | The release of YAP/TAZ in the complex contributes to Wnt/β-catenin signal transduction. |
[96] | 2015.06 | DVL | As a WNT signaling pathway, DVL promotes complex assembly and downstream signal transduction, and also serves as a linker to recruit ZNRF3 and RNF43 to WNT co-receptors to promote their degradation and down-regulation. |
[97] | 2020.12 | Lgr5 | Wnt/β-catenin signaling realizes bile duct regeneration by regulating the expression of Lgr5 gene in ductal response cells (DRCs) located near peribiliary glands. |
[72] | 2021.02 | TMEM9 | Transmembrane protein 9 (TMEM9) is a Wnt signal amplifier, and Tmem9 knockout will damage liver regeneration. |
[98] | 2022.02 | Wnt2 | C-kit + SECs promotes liver partition and regeneration through Wnt2, and is regulated by Notch signal transduction. |
[99] | 2022.03 | TCF1 、LEF1 | TCF1 and its homologue LEF1 have historically been called effective transcription factors downstream of wnt signaling pathway, which are essential for early T cell development. |
[100] | 2023.04 | Wnt/β-catenin | Wnt/β-catenin pathway is activated in the early stage of LR, and the conditional loss of β-catenin liver cells will delay LR. |
[101] | 2023.10 | Wnt/β-catenin | Activation of Wnt/β-catenin signal transduction is the main mitogenic clue of adult primary human hepatocytes. |
[102] | 2023.12 | Wnt | Cell maturation is mediated by the activation of NF-κ в and the inhibition of Wnt signal respectively. |
[103] | 2024.05 | Cachd1 | Cachd1 can bind to both Lrp6 and Wnt co-receptors of Frizzled family. |