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Oncogenic microRNA-27a is a target for anticancer agent methyl 2-cyano-3,11-dioxo-18β-olean-1,12-dien-30-oate in colon cancer cells

Cited 109 time in Web of Science Cited 115 time in Scopus
Authors

Chintharlapalli, Sudhakar; Papineni, Sabitha; Abdelrahim, Maen; Abudayyeh, Ala; Jutooru, Indira; Chadalapaka, Gayathri; Wu, Fei; Mertens-Talcott, Susanne; Vanderlaag, Kathy; Cho, Sung Dae; Smith, Roger, III; Safe, Stephen

Issue Date
2009-10
Publisher
John Wiley & Sons Inc.
Citation
International Journal of Cancer, Vol.125 No.8, pp.1965-1974
Abstract
Methyl 2-cyano-3,11-dioxo-18 beta-olean-1,12-dien-30-oate (CDODA-Me) is a synthetic derivative of glycyrrhetinic acid, a triterpenoid phytochemical found in licorice extracts. CDODA-Me inhibited growth of RKO and SW480 colon cancer cells and this was accompanied by decreased expression of Sp1, Sp3 and Sp4 protein and mRNA and several Sp-dependent genes including survivin, vascular endothelial growth factor (VEGF), and VEGF receptor 1 (VEGFR1 or Flt-1). CDODA-Me also induced apoptosis, arrested RKO and SW480 cells at G(2)/M, and inhibited tumor growth in athymic nude mice bearing RKO cells as xenografts. CDODA-Me decreased expression of microRNA-27a (miR-27a), and this was accompanied by increased expression of 2 miR-27a-regulated mRNAs, namely ZBTB10 (an Sp repressor) and Myt-1 which catalyzes phosphorylation of cdc2 to inhibit progression of cells through G(2)/M. Both CDODA-Me and antisense miR-27a induced comparable responses in RKO and SW480 cells, suggesting that the potent anticarcinogenic activity of CDODA-Me is due to repression of oncogenic miR-27a. (C) 2009 UICC
ISSN
0020-7136
URI
https://hdl.handle.net/10371/208975
DOI
https://doi.org/10.1002/ijc.24530
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  • School of Dentistry
  • Department of Dentistry
Research Area Discovery of molecular targets related to oral cancer metastasis and identification of signal transduction system, Identifying the role of immunological tolerance in oral cancer, Presenting a new concept oral cancer prevention and treatment strategy through identification of major molecular targets and mechanisms related to oral cancer development, 구강암 발병관련 주요 분자표적 및 기전 규명을 통한 신개념 구강암 예방 및 치료전략 제시, 구강암 전이관련 분자표적 발굴 및 신호전달체계 규명, 구강암에서 면연관용의 역할 규명

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