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咖啡豆醇通过ERK信号通路抑制非小细胞肺癌细胞中的BTF3表达来诱导细胞凋亡。

Kahweol induces apoptosis by suppressing BTF3 expression through the ERK signaling pathway in non-small cell lung cancer cells.

作者信息

Jeon Young-Joo, Bang Woong, Cho Jin Hyoung, Lee Ra Ham, Kim Seok-Ho, Kim Minseok S, Park Seon-Min, Shin Jae-Cheon, Chung Hak-Jae, Oh Keon Bong, Seo Jae-Min, Ko Sungho, Shim Jung-Hyun, Chae Jung-Il

机构信息

Department of Dental Pharmacology, School of Dentistry, BK21 Plus, Chonbuk National University, Jeonju, Jeolla 561‑756, Republic of Korea.

Aging Research Institute, Korea Research Institute of Bioscience and Biotechnology, Yuseong, Daejeon, Republic of Korea.

出版信息

Int J Oncol. 2016 Dec;49(6):2294-2302. doi: 10.3892/ijo.2016.3727. Epub 2016 Oct 12.

DOI:10.3892/ijo.2016.3727
PMID:27748804
Abstract

Kahweol, a diterpene molecule, has antiproliferative effects on several types of human cancer cells, but whether it has apoptotic effect in non-small cell lung cancer (NSCLC) is not known. To explore this possibility, we incubated cells from two NSCLC cell lines, NCI-H358 and NCI‑H1299, with different concentrations of kahweol and used the MTS assay, DAPI staining, propidium iodide staining, Annexin V staining, immunocytochemical test, and western blot analysis to characterize this molecule and the signaling pathway underlying its effects. The kahweol-treated cells showed significantly decreased cell viability, increased nuclear condensation, and an increased number of Annexin V-positive NSCLC cells. Suppression of basic transcription factor 3 (BTF3) was followed by apoptosis induced by kahweol via the ERK-mediated signaling pathway in a dose- and time-dependent manner. In addition, kahweol modulated the protein expression of BTF3 genes involved in cell-cycle regulation and apoptosis-related proteins, resulting in apoptotic cell death. Our results collectively indicated that kahweol inhibited the proliferation of NSCLC cells through ERK-mediated signaling pathways and the downregulation of BTF3.

摘要

咖啡豆醇是一种二萜类分子,对多种人类癌细胞具有抗增殖作用,但它在非小细胞肺癌(NSCLC)中是否具有凋亡作用尚不清楚。为了探究这种可能性,我们用不同浓度的咖啡豆醇处理了两种NSCLC细胞系NCI-H358和NCI-H1299的细胞,并使用MTS检测、DAPI染色、碘化丙啶染色、膜联蛋白V染色、免疫细胞化学检测和蛋白质印迹分析来表征该分子及其作用背后的信号通路。经咖啡豆醇处理的细胞显示出细胞活力显著降低、核浓缩增加以及膜联蛋白V阳性NSCLC细胞数量增加。在咖啡豆醇通过ERK介导的信号通路以剂量和时间依赖性方式诱导凋亡后,基础转录因子3(BTF3)受到抑制。此外,咖啡豆醇调节了参与细胞周期调控的BTF3基因以及凋亡相关蛋白的表达,导致细胞凋亡死亡。我们的结果共同表明,咖啡豆醇通过ERK介导的信号通路和BTF3的下调抑制了NSCLC细胞的增殖。

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