Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Chenci Wang"'
Autor:
Tao Chen, Jiayi Zhou, Jiangang Liu, Jianwei Wang, Zhuohao Liu, Jie Mao, Dinglan Wu, Xiaosheng He, Chenci Wang, Zhengwei Wang, Jiani Lin, Tingzheng Pan, Hongchao Xu
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 12, Iss 8 (2024)
Background Oxylipin metabolism plays an essential role in glioma progression and immune modulation in the tumor microenvironment. Lipid metabolic reprogramming has been linked to macrophage remodeling, while the understanding of oxylipins and their c
Externí odkaz:
https://doaj.org/article/ea377cbc6837404f9d90a6ff7f17f66b
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-23 (2024)
Abstract Coagulation factor 2 thrombin receptor (F2R), a member of the G protein-coupled receptor family, plays an important role in regulating blood clotting through protein hydrolytic cleavage mediated receptor activation. However, the underlying b
Externí odkaz:
https://doaj.org/article/8a7720f46fbc4b6c9d3cc5fe987a1d90
Autor:
Xinzhi Yang, Jiangang Liu, Chenci Wang, Kenneth King-yip Cheng, Hongchao Xu, Qingzhong Li, Tian Hua, Xue Jiang, Lili Sheng, Jie Mao, Zhuohao Liu
Publikováno v:
Oncogenesis, Vol 10, Iss 2, Pp 1-13 (2021)
Abstract The development of glioblastoma (GBM) is typically accompanied by marked changes in lipid metabolism. Oxylipins and their catalyzed enzymes lipoxygenases (LOXs) have been shown to participate in the development of cancers via multiple pathwa
Externí odkaz:
https://doaj.org/article/ccdca560a3b24a50b54f7ed60998185d
Publikováno v:
Archivos Españoles de Urología; 2024, Vol. 77 Issue 3, p242-248, 7p
Publikováno v:
Molecular Cancer Research. 21:189-198
Our previous study illustrated that nuclear factor IX (NFIX) promotes glioblastoma (GBM) progression by inducing migration and proliferation of GBM cells. However, the underlying mechanism of how NFIX regulates GBM cell proliferation remains obscure.
Table S1. Primer sequences for mRNA expression analysis. Table S2. Sequences of shRNA. Table S3. Antibodies for immunoblotting.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9099c29552de9e2a59e22debd006b6d
https://doi.org/10.1158/1541-7786.22527980
https://doi.org/10.1158/1541-7786.22527980
S1. Full images of immunoblotting. S2. NFIX knockdown has no effect on p53 and p21 expression. S3. Knockdown of GINS1 by shRNAs in U87 cells. S4. Knockdown of GINS1 represses proliferation of GL261 cells S5. GINS1 rescues the delayed growth of NFIX-n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb59487ce31ba5af09f6121de22727fa
https://doi.org/10.1158/1541-7786.22527983.v1
https://doi.org/10.1158/1541-7786.22527983.v1
Autor:
Tian Hua, Lili Sheng, Zhuohao Liu, Xue Jiang, Qingzhong Li, Chenci Wang, Jie Mao, Jiangang Liu, Kenneth K.Y. Cheng, Xinzhi Yang, Hongchao Xu
Publikováno v:
Oncogenesis
Oncogenesis, Vol 10, Iss 2, Pp 1-13 (2021)
Oncogenesis, Vol 10, Iss 2, Pp 1-13 (2021)
The development of glioblastoma (GBM) is typically accompanied by marked changes in lipid metabolism. Oxylipins and their catalyzed enzymes lipoxygenases (LOXs) have been shown to participate in the development of cancers via multiple pathways, while