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ABSTRACT: Background
The tumor suppressor FBW7 is the substrate recognition component of the SCF E3-ubiquitin ligase complex that mediates proteolytic degradation of various oncogenic proteins. However, the role of FBW7 in ovarian cancer progression remains inadequately understood.Methods
IP-MASS, co-IP, immunohistochemistry, and western blotting were used to identify the potential substrate of FBW7 in ovarian cancer. The biological effects of FBW7 were investigated using in vitro and in vivo models. LC/MS was used to detect the m6A levels in ovarian cancer tissues. MeRIP-Seq and RNA-Seq were used to assess the downstream targets of YTHDF2.Results
We unveil that FBW7 is markedly down-regulated in ovarian cancer tissues and its high expression is associated with fav
SUBMITTER: Xu F
PROVIDER: S-EPMC7927415 | biostudies-literature | 2021 Mar
REPOSITORIES: biostudies-literature