Garcinia Benzophenones Inhibit the Growth of Human Colon Cancer Cells and Synergize with Sulindac Sulfide and Turmeric

被引:12
作者
Einbond, Linda Saxe [1 ,2 ,3 ,4 ]
Mighty, Jason [2 ,3 ]
Kashiwazaki, Ryota [1 ]
Figueroa, Mario [2 ,3 ,5 ]
Jalees, Filza [2 ,3 ]
Acuna, Ulyana Munoz [2 ,3 ]
LeGendre, Onica [6 ,7 ]
Foster, David A. [6 ,7 ]
Kennelly, Edward J. [2 ,3 ]
机构
[1] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
[2] CUNY Herbert H Lehman Coll, Bronx, NY 10468 USA
[3] CUNY, Grad Ctr, Bronx, NY 10468 USA
[4] New York Bot Garden, New York, NY 10458 USA
[5] Univ Nacl Autonoma Mexico, Fac Quim, Mexico City 04510, DF, Mexico
[6] CUNY Hunter Coll, New York, NY 10065 USA
[7] CUNY, Grad Ctr, New York, NY 10065 USA
关键词
Benzophenone; celecoxib; endoplasmic reticulum; Garcinia; rapamycin; sulindac sulfide; and turmeric; synergy; POLYISOPRENYLATED BENZOPHENONES; ENDOPLASMIC-RETICULUM; SIGNAL-TRANSDUCTION; PREVENTION; RAPAMYCIN; RATS; CARCINOGENESIS; POLYPHENOLS; COUMARINS; APOPTOSIS;
D O I
10.2174/18715206113139990095
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Previous studies indicate that extracts and purified components from Garcinia species inhibit the growth of human colon cancer cells. Garcinia benzophenones activate the expression of genes in the endoplasmic reticulum and cellular energy stress (mTOR) pathways. This study examines the growth inhibitory and synergistic effects of Garcinia benzophenones, alone or combined with chemopreventive agents, on human colon cancer cells. To find optimal combination treatments, HT29 colon cancer cells were treated with benzophenones alone, or combined with chemopreventive agents, and cell growth measured using the MTT assay. To reveal effects on signaling pathways, we assessed effects of the MEK inhibitor U0126 and the ER IP3 receptor antagonist heparin, as well as effects on the phosphorylation of 4E-BP-1 (mTOR pathway), using Western blot analysis. New and known benzophenones from Garcinia intermedia inhibited the growth of human colon cancer cells; an alcohol extract of Garcinia xanthochymus, as well as purified guttiferones (guttiferone E and xanthochymol), preferentially inhibited the growth of colon cancer versus nonmalignant intestinal epithelial cells. Guttiferone E exhibited synergy with the NSAID sulindac sulfide and xanthochymol, with the spice turmeric. Guttiferone A did not alter phosphorylation of 4E-BP-1, indicating that the mTORC1 pathway is not involved in its action. The effects of xanthochymol were enhanced by U0126, at low doses, and were blocked by heparin, indicating that the MEK pathway is involved, while the ER IP3 receptor is critical for its action. These studies indicate the potential of benzophenones, alone or combined with sulindac sulfide or turmeric, to prevent and treat colon cancer.
引用
收藏
页码:1540 / 1550
页数:11
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