Novel ent-Kaurane Diterpenoid from Rubus corchorifolius L. f. Inhibits Human Colon Cancer Cell Growth via Inducing Cell Cycle Arrest and Apoptosis

被引:28
作者
Chen, Xuexiang [1 ,2 ,3 ]
Wu, Xian [2 ]
Ouyang, Wen [5 ]
Gu, Min [2 ]
Gao, Zili [2 ]
Song, Mingyue [2 ]
Chen, Yunjiao [1 ,4 ]
Lin, Yanyin [1 ,4 ]
Cao, Yong [1 ,4 ]
Xiao, Hang [2 ]
机构
[1] South China Agr Univ, Coll Food Sci, Guangzhou 510642, Guangdong, Peoples R China
[2] Univ Massachusetts, Dept Food Sci, Amherst, MA 01003 USA
[3] Guangzhou Med Univ, Coll Publ Hlth, Guangzhou 511436, Guangdong, Peoples R China
[4] Guangdong Prov Engn Res Ctr Bioact Nat Prod, Guangzhou 510642, Guangdong, Peoples R China
[5] Hunan Univ Tradit Chinese Med, Coll Pharm, Changsha 410007, Hunan, Peoples R China
关键词
Rubus corchorifolius L.f; ent-kaur-2-one-16; beta; 17-dihydroxy-acetone-ketal; colon cancer; cell cycle; apoptosis; COLORECTAL-CANCER; PATHWAYS; DIFFERENTIATION; IDENTIFICATION; PROLIFERATION; CHEMOTHERAPY; CLEAVAGE;
D O I
10.1021/acs.jafc.6b05376
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The tender leaves of Rubus corchorifolius L. f. have been consumed as tea for drinking in China since ancient times. In this study, a novel ent-kaurane diterpenoid was isolated and identified from R corchorifolius L. f. leaves as ent-kaur-2-one16 beta,17-dihydroxy-acetone-ketal (DEK). DEK suppressed the growth of HCT116 human colon cancer cells with an IC50 value of 40 +/- 0.21 yM, while it did not cause significant growth inhibition on CCD-18Co human colonic myofibroblasts at up to100 mu M. Moreover, DEK induced extensive apoptosis and S phase cell cycle arrest in the colon cancer cells. Accordingly, DEK caused profound effects on multiple signaling proteins associated with cell proliferation, cell death, and inflammation. DEK significantly upregulated the expression levels of pro-apoptotic proteins such as cleaved caspase-3, cleaved caspase-9, cleaved PARP, p53, Bax, and tumor suppressor p21(ciPl/Waf1), downregulated the levels of cell cycle regulating proteins such as cyclinD1, CDK2, and CDK4 and carcinogenic proteins such as EGFR and COX-2, and suppressed the activation of Akt. Overall, our results provide a basis for using DEK as a potential chemopreventive agent against colon carcinogenesis.
引用
收藏
页码:1566 / 1573
页数:8
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