Literature DB >> 17303010

Mechanisms of antiprostate cancer by gum mastic: NF-kappaB signal as target.

Mei-Lan He1, Ang Li, Chun-Su Xu, Shun-Li Wang, Meng-Jie Zhang, Hua Gu, Yao-Qin Yang, Hui-Hong Tao.   

Abstract

AIM: To study the effect of gum mastic, a natural resin, on the proliferation of androgen-independent prostate cancer PC-3 cells, and further investigate the mechanisms involved in this regulatory system, taking nuclear factor kappaB (NF-kappaB) signal as the target.
METHODS: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and a flow cytometer were used to detect the effect of gum mastic on the proliferation of PC-3 cells. Then, reporter gene assay, RT-PCR, and Western blotting were carried out to study the effects of gum mastic on the NF-kappaB protein level and the NF-kappaB signal pathway. The expression of genes involved in the NF-kappaB signal pathway, including cyclin D1, inhibitors of kappaBs (I kappaB alpha), and phosphorylated Akt (p-AKT), were measured. In addition, transient transfection assays with the 5X NF-kappaB consensus sequence promoter was also used to test the effects of gum mastic.
RESULTS: Gum mastic inhibited PC-3 cell growth and blocked the PC-3 cell cycle in the G1 phase. Gum mastic also suppressed NF-kappaB activity in the PC-3 cells. The expression of cyclin D1, a crucial cell cycle regulator and an NF-kappaB downstream target gene, was reduced as well. Moreover, gum mastic decreased the p-AKT protein level and increased the I kappa B alpha protein level.
CONCLUSION: Gum mastic inhibited the proliferation and blocked the cell cycle progression in PC-3 cells by suppressing NF-kappaB activity and the NF-kappaB signal pathway.

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Year:  2007        PMID: 17303010     DOI: 10.1111/j.1745-7254.2007.00536.x

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


  19 in total

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Authors:  Xin-yu Huang; Hong-cheng Wang; Zhou Yuan; Ang Li; Mei-lan He; Kai-xing Ai; Qi Zheng; Huan-long Qin
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7.  A transcriptomic computational analysis of mastic oil-treated Lewis lung carcinomas reveals molecular mechanisms targeting tumor cell growth and survival.

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8.  Induction of G1 cell cycle arrest and cyclin D1 down-regulation in response to pericarp extract of Baneh in human breast cancer T47D cells.

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9.  Mastic oil inhibits the metastatic phenotype of mouse lung adenocarcinoma cells.

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Journal:  Cancers (Basel)       Date:  2011-02-23       Impact factor: 6.639

10.  Evaluation of the genotoxic and antigenotoxic effects of Chios mastic water by the in vitro micronucleus test on human lymphocytes and the in vivo wing somatic test on Drosophila.

Authors:  Dimitris Vlastos; Despoina Mademtzoglou; Elena Drosopoulou; Ioanna Efthimiou; Tatiana Chartomatsidou; Christina Pandelidou; Melina Astyrakaki; Eleftheria Chalatsi; Penelope Mavragani-Tsipidou
Journal:  PLoS One       Date:  2013-07-23       Impact factor: 3.240

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