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Role of transcription factor Sp1 in the quercetin-mediated inhibitory effect on human malignant pleural mesothelioma

Authors
Chae, Jung-IlCho, Jin HyoungLee, Kyung-AeChoi, Nag-JinSeo, Kang SeokKim, Sang-BumLee, Sang-HanShim, Jung-Hyun
Issue Date
Oct-2012
Publisher
Demetrios A. Spandidos Ed. & Pub.
Keywords
quercetin; apoptosis; specificity protein 1; human malignant pleural mesothelioma; anticancer
Citation
International Journal of Molecular Medicine, v.30, no.4, pp 835 - 841
Pages
7
Journal Title
International Journal of Molecular Medicine
Volume
30
Number
4
Start Page
835
End Page
841
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/14818
DOI
10.3892/ijmm.2012.1075
ISSN
1107-3756
1791-244X
Abstract
Quercetin (Qu) is found in plants, including red onions and in the skins of red apples, and induces the apoptosis of certain malignant cells. However, no report has been issued on the apoptotic effect of Qu on human malignant pleural mesothelioma. In the present study, it was found that MSTO-211H mesothelioma cell viability was reduced and apoptotic cell death was increased by Qu (20-80 mu M), which was found to have an IC50 of 58 mu M. In addition, Qu increased the sub-G, cell population, and was found to interact with specificity protein 1 (Sp1) and significantly suppressed its expression at the protein and mRNA levels. Furthermore, Qu modulated the levels of Sp1 regulatory genes, such as cycl in D1, myeloid cell leukemia (Mcl)-1 and survivin in MSTO-211H cells. Apoptotic signaling cascades were activated by the cleavage of Bid, caspase-3 and PARP, and by the downregulation of Bcl-xL and the upregulation of Bax in MSTO-211H cells. Our results strongly suggest that Sp1 be considered as a novel molecular target of Qu in human malignant pleural mesothelioma.
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