The Role of CPNE7 (Copine-7) in Colorectal Cancer Prognosis and Metastasis.
Hye-Jeong KongDong-Hyun KangTae-Sung AhnKwang-Seock KimTae-Wan KimSoo-Hyeon LeeDong-Woo LeeJae-Sung RyuMoo-Jun BeakPublished in: International journal of molecular sciences (2023)
Colorectal cancer (CRC) is one of the most common and deadly cancers in the world. However, no effective treatment for the disease has yet been found. For this reason, several studies are being carried out on the treatment of CRC. Currently, there is limited understanding of the role of CPNE7 (copine-7) in CRC progression and metastasis. The results of this study show that CPNE7 exerts an oncogenic effect in CRC. First, CPNE7 was shown to be significantly up-regulated in CRC patient tissues and CRC cell lines compared to normal tissues according to IHC staining, qRT-PCR, and western blotting. Next, this study used both systems of siRNA and shRNA to suppress CPNE 7 gene expression to check the CPNE7 mechanism in CRC. The suppressed CPNE7 significantly inhibited the growth of CRC cells in in vitro experiments, including migration, invasion, and semisolid agar colony-forming assay. Moreover, the modified expression of CPNE7 led to a decrease in the levels of genes associated with epithelial-mesenchymal transition (EMT). The epithelial genes E-cadherin ( CDH1 ) and Collagen A1 were upregulated, and the levels of mesenchymal genes such as N-cadherin (CDH2) , ZEB1 , ZEB2 , and SNAIL ( SNAL1 ) were downregulated after CPNE7 inhibition. This study suggests that CPNE7 may serve as a potential diagnostic biomarker for CRC patients.
Keyphrases
- epithelial mesenchymal transition
- gene expression
- stem cells
- induced apoptosis
- signaling pathway
- end stage renal disease
- transforming growth factor
- transcription factor
- dna methylation
- genome wide
- south africa
- bone marrow
- chronic kidney disease
- poor prognosis
- cell migration
- oxidative stress
- combination therapy
- cell death
- climate change
- cell proliferation
- cancer therapy
- cell cycle arrest
- genome wide identification
- cell adhesion