Overexpression of Nrf2 promotes colon cancer progression via ERK and AKT signaling pathways

被引:27
|
作者
Lee, Yoon Jin [1 ]
Kim, Woo Il [1 ]
Bae, Jin Ho [1 ]
Cho, Moon Kyun [1 ]
Lee, Sang Han [1 ]
Nam, Hae Seon [1 ]
Choi, In Ho [1 ]
Cho, Sung Woo [2 ]
机构
[1] Soonchunhyang Univ, Coll Med, Mol Canc Res, Cheonan, South Korea
[2] Soonchunhyang Univ, Dept Surg, Seoul Hosp, 59 Daesahwan Ro, Seoul 04401, South Korea
关键词
Colorectal neoplasms; NF-E2-related factor 2; Reactive oxygen species; PROTEASOME ACTIVITY; COLORECTAL-CANCER; FACTOR-2; NRF2; ACTIVATION; EXPRESSION; CELLS; CARCINOGENESIS; MUTATIONS; SURVIVAL; FEATURES;
D O I
10.4174/astr.2020.98.4.159
中图分类号
R61 [外科手术学];
学科分类号
摘要
Purpose: We investigated the expression of Nrf2 in colorectal cancer and its correlation with clinicopathological characteristics as well as mechanisms and roles of Nrf2 expression including cell signaling pathway, survival, proliferation, and migration. Methods: Nrf2 expression was measured in 12 and 30 different colorectal cancer (CRC) tissues by western blot (WB) and immunohistochemistry (IHC), respectively. SW480 cells were used for cell proliferation and cell migration tests. The correlation between the expression of Nrf2 and clinicopathologic parameters were evaluated using the chi-square or Fisher exact test. Data are expressed as the mean +/- standard deviation for 3 independent experiments. P < 0.05 was considered statistically significant. Results: Analysis of WB demonstrated that Nrf2 proteins were increased in CRC tissues, and decreased in normal tissues. IHC staining showed that the Nrf2 expression was elevated in CRC tissues, compared to matched normal tissues. When SW480 cells were suppressed with small interfering RNA of Nrf2, cell viability was inhibited, and cell apoptosis was increased. These results were found along with suppression of the phosphorylated form of extracellular signal-regulated kinase 1/2 and AKT. Conclusion: This study suggests that overexpression of Nrf2 may be related to carcinogenesis and progression of CRC.
引用
收藏
页码:159 / 167
页数:9
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