Euonymus sachalinensis Induces Apoptosis by Inhibiting the Expression of c-Myc in Colon Cancer Cells

被引:0
|
作者
Park, So-Mi [1 ,2 ]
Jee, Wona [1 ,2 ]
Park, Ye-Rin [1 ,2 ]
Kim, Hyungsuk [3 ]
Na, Yun-Cheol [4 ]
Jung, Ji Hoon [1 ,2 ]
Jang, Hyeung-Jin [1 ,2 ]
机构
[1] Kyung Hee Univ, Coll Korean Med, 26 Kyungheedae Ro, Seoul 02447, South Korea
[2] Kyung Hee Univ, Grad Sch, Dept Sci Korean Med, Seoul 02447, South Korea
[3] Kyung Hee Univ, Dept Korean Rehabil Med, Med Ctr, Seoul 02447, South Korea
[4] Korea Basic Sci Inst, Western Seoul Ctr, 150 Bugahyeon Ro, Seoul 03759, South Korea
来源
MOLECULES | 2023年 / 28卷 / 08期
基金
新加坡国家研究基金会;
关键词
Euonymus sachalinensis; colon cancer; c-Myc; apoptosis; oncogene; anti-cancer; AMPLIFICATION; ALKALOIDS; ONCOGENE; EXTRACTS; STEMS;
D O I
10.3390/molecules28083473
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We hypothesized that Euonymus sachalinensis (ES) induces apoptosis by inhibiting the expression of c-Myc in colon cancer cells, and this study proved that the methanol extract of ES has anticancer effects in colon cancer cells. ES belongs to the Celastraceae family and is well known for its medicinal properties. Extracts of species belonging to this family have been used to treat diverse diseases, including rheumatoid arthritis, chronic nephritis, allergic conjunctivitis, rhinitis, and asthma. However, ES has been targeted because there are currently few studies on the efficacy of ES for various diseases, including cancer. ES lowers cell viability in colon cancer cells and reduces the expression of c-Myc protein. We confirm that the protein level of apoptotic factors such as PARP and Caspase 3 decrease when ES is treated with Western blot, and confirm that DNA fragments occur through TUNEL assay. In addition, it is confirmed that the protein level of oncogenes CNOT2 and MID1IP1 decrease when ES is treated. We have also found that ES enhances the chemo-sensitivity of 5-FU in 5-FU-resistant cells. Therefore, we confirm that ES has anticancer effects by inducing apoptotic cell death and regulating the oncogenes CNOT2 and MID1IP1, suggesting its potential for use in the treatment of colon cancer.
引用
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页数:13
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