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result sql = Apoptotic effect of quercetin on HT-29 colon cancer cells via the AMPK signaling pathway.
Apoptotic effect of quercetin on HT-29 colon cancer cells via the AMPK signaling pathway.
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result sql = Activation of AMP-activated protein kinase (AMPK), a physiological cellular energy sensor, strongly suppresses cell proliferation in both nonmalignant and tumor cells. This study demonstrates the mechanism of quercetin-induced apoptosis in HT-29 colon cancer cells. Treatment of cells with quercetin significantly decreased cell viability in a dose-dependent manner. Notably, quercetin increased cell cycle arrest in the G1 phase and up-regulated apoptosis-related proteins, such as AMPK, p53, and p21, within 48 h. Furthermore, in vivo experiments showed that quercetin treatment resulted in a significant reduction in tumor volume over 6 weeks, and apoptosis-related protein induction by quercetin was significantly higher in the 100 mg/kg treated group compared to the control group. All of these results indicate that quercetin induces apoptosis via AMPK activation and p53-dependent apoptotic cell death in HT-29 colon cancer cells and that it may be a potential chemopreventive or therapeutic agent against HT-29 colon cancer.

Publication: J. Agric. Food Chem. 2010 Aug 11 ;58(15)::8643-50. :doi: 10.1021/jf101510z.
Publication Date: 2010 Aug 11
Study Author(s): Kim, Hyeong-Jin;Kim, Sang-Ki;Kim, Byeong-Soo;Lee, Seung-Ho;Park, Young-Seok;Park, Byung-Kwon;Kim, So-Jung;Kim, Jin;Choi, Changsun;Kim, Jong-Suk;Cho, Sung-Dae;Jung, Ji-Won;Roh, Kyong-Hwan;Kang, Kyung-Sun;Jung, Ji-Youn;
Institution: Department of Companion and Laboratory Animal Science, Kongju National University, 340-702 Yesan, Republic of Korea.
Shortcut link to this study:
Activation of AMP-activated protein kinase (AMPK), a physiological cellular energy sensor, strongly suppresses cell proliferation in both nonmalignant and tumor cells. This study demonstrates the mechanism of quercetin-induced apoptosis in HT-29 colon cancer cells. Treatment of cells with quercetin significantly decreased cell viability in a dose-dependent manner. Notably, quercetin increased cell cycle arrest in the G1 phase and up-regulated apoptosis-related proteins, such as AMPK, p53, and p21, within 48 h. Furthermore, in vivo experiments showed that quercetin treatment resulted in a significant reduction in tumor volume over 6 weeks, and apoptosis-related protein induction by quercetin was significantly higher in the 100 mg/kg treated group compared to the control group. All of these results indicate that quercetin induces apoptosis via AMPK activation and p53-dependent apoptotic cell death in HT-29 colon cancer cells and that it may be a potential chemopreventive or therapeutic agent against HT-29 colon cancer.
PMID: 20681654

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