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2,3,6-Tribromo-4,5-dihydroxybenzyl Methyl Ether Induces Growth Inhibition and Apoptosis in MCF-7 Human Breast Cancer Cells
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  • 2,3,6-Tribromo-4,5-dihydroxybenzyl Methyl Ether Induces Growth Inhibition and Apoptosis in MCF-7 Human Breast Cancer Cells
  • 2,3,6-Tribromo-4,5-dihydroxybenzyl Methyl Ether Induces Growth Inhibition and Apoptosis in MCF-7 Human Breast Cancer Cells
저자명
Lee. Ji-Hyeon,Park. Sang-Eun,Hossain. Mohammad Akbar,Kim. Min-Young,Kim. Mi-Na,Chung. Hae-Young,Choi. Jae-Sue,Yoo. Young-Hyun,Ki
간행물명
Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea
권/호정보
2007년|30권 9호|pp.1132-1137 (6 pages)
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대한약학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

In this study, we investigated the effects of 2,3,6-tribromo-4,5-dihydroxybenzyl methyl ether (TDB), isolated from Symphyocladia latiuscula (marine red algae), on the proliferation of MCF-7 human breast cancer cells. TDB treatment for 48 h inhibited cancer cell growth and induced DNA fragmentation. Furthermore, morphological characterizations such as apoptotic bodies and membrane blebs were shown by electronic microscopy. TDB-induced apoptosis in the MCF-7 cells was closely linked with the down-regulation of Bcl-2 protein expression and the cleavage of caspase-3 substrates, with poly(ADP-ribose) polymerase cleavage occurring by TDB treatment. TDB treatment also caused a marked increase in the level of $p21^{WAF1/CIP1}$ protein in a p53-dependent manner. In addition, the upregulation of$p21^{WAF1/CIP1}$ in the MCF-7 cells was related to a decrease in c-Myc protein in a dose-dependent manner. Based on our data, TDB is a good candidate for further evaluation as an effective chemotherapeutic agent, acting through the induction of apoptosis.