Esculetin exerts anti-proliferative effects against non-small-cell lung carcinoma by suppressing specificity protein 1 in vitro

Esculetin, a coumarin derivative, is a phenolic compound isolated from Artemisia capillaris, Citrus limonia, and Euphorbia lathyris. Although it has been reported to have anti-inflammatory, anti-oxidant, and anti-proliferative activities in several human cancers, its anti-proliferative activity agai...

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Veröffentlicht in:General physiology and biophysics 2017-01, Vol.36 (1), p.31-39
Hauptverfasser: Lee, Ra H, Jeon, Young-Joo, Cho, Jin H, Jang, Jeong-Yun, Kong, Il-Keun, Kim, Seok-Ho, Kim, MinSeok S, Chung, Hak-Jae, Oh, Keon B, Park, Seon-Min, Shin, Jae-Cheon, Seo, Jae-Min, Ko, Sungho, Shim, Jung-Hyun, Chae, Jung-Il
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container_end_page 39
container_issue 1
container_start_page 31
container_title General physiology and biophysics
container_volume 36
creator Lee, Ra H
Jeon, Young-Joo
Cho, Jin H
Jang, Jeong-Yun
Kong, Il-Keun
Kim, Seok-Ho
Kim, MinSeok S
Chung, Hak-Jae
Oh, Keon B
Park, Seon-Min
Shin, Jae-Cheon
Seo, Jae-Min
Ko, Sungho
Shim, Jung-Hyun
Chae, Jung-Il
description Esculetin, a coumarin derivative, is a phenolic compound isolated from Artemisia capillaris, Citrus limonia, and Euphorbia lathyris. Although it has been reported to have anti-inflammatory, anti-oxidant, and anti-proliferative activities in several human cancers, its anti-proliferative activity against non-small-cell lung carcinoma (NSCLC) and the molecular mechanisms involved have not been adequately elucidated. In this study, we used two NSCLC cell lines (NCI-H358 and NCI-H1299) to investigate the anti-proliferative activity and apoptotic effect of esculetin. Our data showed that esculetin-treated cells exhibited reduced proliferation and apoptotic cell morphologies. Intriguingly, the transcription factor specificity protein 1 (Sp1) was significantly suppressed by esculetin in a dose- and time-dependent manner. Furthermore, the levels of p27 and p21, two key regulators of the cell cycle, were up-regulated by the esculetin-mediated down-regulation of Sp1; the level of a third cell-cycle regulator, survivin, was decreased, resulting in caspase-dependent apoptosis. Therefore, we conclude that esculetin could be a potent anti-proliferative agent in patients with NSCLC.
doi_str_mv 10.4149/gpb_2016024
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Although it has been reported to have anti-inflammatory, anti-oxidant, and anti-proliferative activities in several human cancers, its anti-proliferative activity against non-small-cell lung carcinoma (NSCLC) and the molecular mechanisms involved have not been adequately elucidated. In this study, we used two NSCLC cell lines (NCI-H358 and NCI-H1299) to investigate the anti-proliferative activity and apoptotic effect of esculetin. Our data showed that esculetin-treated cells exhibited reduced proliferation and apoptotic cell morphologies. Intriguingly, the transcription factor specificity protein 1 (Sp1) was significantly suppressed by esculetin in a dose- and time-dependent manner. Furthermore, the levels of p27 and p21, two key regulators of the cell cycle, were up-regulated by the esculetin-mediated down-regulation of Sp1; the level of a third cell-cycle regulator, survivin, was decreased, resulting in caspase-dependent apoptosis. Therefore, we conclude that esculetin could be a potent anti-proliferative agent in patients with NSCLC.</abstract><cop>Slovakia</cop><pmid>27901471</pmid><doi>10.4149/gpb_2016024</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Antineoplastic Agents - pharmacology
Antioxidants - pharmacology
Carcinoma, Non-Small-Cell Lung - drug therapy
Carcinoma, Non-Small-Cell Lung - metabolism
Carcinoma, Non-Small-Cell Lung - pathology
Cell Proliferation - drug effects
Dose-Response Relationship, Drug
Down-Regulation - drug effects
Lung Neoplasms - drug therapy
Lung Neoplasms - metabolism
Lung Neoplasms - pathology
Sp1 Transcription Factor - metabolism
Umbelliferones - pharmacology
title Esculetin exerts anti-proliferative effects against non-small-cell lung carcinoma by suppressing specificity protein 1 in vitro
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