Yao TANG, Debing XIANG, Jie WANG, et al. Proline-rich protein 11 is highly expressed in colorectal cancer to promote cancer cell invasion and metastasis[J]. Journal of Third Military Medical University, 2019, 41(22): 2181-2189.
DOI:
Yao TANG, Debing XIANG, Jie WANG, et al. Proline-rich protein 11 is highly expressed in colorectal cancer to promote cancer cell invasion and metastasis[J]. Journal of Third Military Medical University, 2019, 41(22): 2181-2189. DOI: 10.16016/j.1000-5404.201907034.
Proline-rich protein 11 is highly expressed in colorectal cancer to promote cancer cell invasion and metastasis
To investigate the expression of proline-rich protein 11 (PRR11) in colorectal cancer and its role in regulating the invasion and metastasis of colorectal cancer.
Methods
2
The expression of PRR11 was detected using immunohistochemical SP method in 136 specimens of colorectal cancer tissues and 68 adjacent tissues collected from Jiangjin District Central Hospital between January
2015 and March
2018. We also examined the expression of PRR11 and epithelial-mesenchymal transition (EMT)-related signal molecules in 3 colorectal cancer cell lines (SW480
HT29 and HCT116) and normal human rectal epithelial cells (HCoEpiC) using Western blotting
RT-PCR and immunofluorescence assay; cell scratch assay and Transwell assay were used to compare the migration and invasion abilities of the colorectal cancer cells.
Results
2
The positive expression rate of PRR11 was significantly higher in colorectal cancer tissue than in the adjacent tissues (60.29%
vs
1.47%
P
<
0.01). PRR11 expression was significantly correlated with tumor differentiation
distant metastasis
tumor size and tumor staging (
P
<
0.05). Compared with normal colorectal epithelial cells
the colorectal cancer cell lines expressed high levels of PRR11. Overexpression of PRR11 in HT29 cells significantly enhanced the cell migration and invasion ability
caused obvious β-catenin nuclear translocation
significantly up-regulated the expression of β-catenin and vimentin
and decreased the expression of E-cadherin (
P
<
0.05). Silencing PRR11 significantly lowered the migration and invasion ability of HT29 cells
decreased the expression of β-catenin and vimentin
and increased the expression of E-cadherin (
P
<
0.05).
Conclusion
2
PRR11 is highly expressed in colorectal cancer to promote tumor invasion and metastasis possibly by promoting the nuclear translocation of β-catenin
via
activating the Wnt/β-catenin signaling pathway.
关键词
Keywords
references
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