YAP1-CPNE3 positive feedback pathway promotes gastric cancer cell progression.
Xuan LiHongguang ZhongQianqian ShiRuiwen RuanChunye HuangQin WenShaocheng ZengYang XiaQinru ZengJianping XiongShanshan WangJun ChenWan LeiJun DengPublished in: Cellular and molecular life sciences : CMLS (2024)
Hippo-Yes-associated protein 1 (YAP1) plays an important role in gastric cancer (GC) progression; however, its regulatory network remains unclear. In this study, we identified Copine III (CPNE3) was identified as a novel direct target gene regulated by the YAP1/TEADs transcription factor complex. The downregulation of CPNE3 inhibited proliferation and invasion, and increased the chemosensitivity of GC cells, whereas the overexpression of CPNE3 had the opposite biological effects. Mechanistically, CPNE3 binds to the YAP1 protein in the cytoplasm, inhibiting YAP1 ubiquitination and degradation mediated by the E3 ubiquitination ligase β-transducin repeat-containing protein (β-TRCP). Thereby activating the transcription of YAP1 downstream target genes, which creates a positive feedback cycle to facilitate GC progression. Immunohistochemical analysis demonstrated significant upregulation of CPNE3 in GC tissues. Survival and Cox regression analyses indicated that high CPNE3 expression was an independent prognostic marker for GC. This study elucidated the pivotal involvement of an aberrantly activated CPNE3/YAP1 positive feedback loop in the malignant progression of GC, thereby uncovering novel prognostic factors and therapeutic targets in GC.
Keyphrases
- transcription factor
- gas chromatography
- signaling pathway
- prognostic factors
- cell proliferation
- poor prognosis
- genome wide identification
- induced apoptosis
- gene expression
- genome wide
- binding protein
- cell death
- dna binding
- oxidative stress
- small molecule
- pi k akt
- copy number
- long non coding rna
- endoplasmic reticulum stress
- liquid chromatography
- solid phase extraction