Literature DB >> 16691616

Gum mastic inhibits the expression and function of the androgen receptor in prostate cancer cells.

Mei-Lan He1, Hui-Qing Yuan, An-Li Jiang, Ai Yu Gong, Wei-Wen Chen, Peng-Ju Zhang, Charles Y F Young, Jian-Ye Zhang.   

Abstract

Accumulating evidence suggests that the androgen receptor (AR) may play an important role in the development and progression of prostate cancer. To find new, useful compounds that effectively may attenuate the function of AR in prostate cancer cells, the authors investigated the effect of gum mastic, a natural resin, on AR activity. An androgen-responsive prostate cancer cell line LNCaP was used as a model for this study. Gene transfer, reverse transcriptase-polymerase chain reaction analysis, electrophoretic mobility shift assay, and Western blot analysis were used to test the effect of gum mastic on the expression and function of the AR. To demonstrate the inhibitory effect of gum mastic on the function of the AR, the expression of androgen-regulated genes, including prostate-specific antigen (PSA), human kallikrein 2 (hK2), and NKX3.1 were measured. In addition, transient transfection assays with the PSA promoter and the AR promoter also were used to test the effects of mastic. The results showed that gum mastic inhibited the expression of the AR at the transcriptional level, resulting in the down-regulation of both AR messenger RNA and protein levels. Therefore, the function of the AR was inhibited, as reflected by the reduced expression of NKX3.1 and PSA and by androgen-stimulated growth. Because gum mastic exhibited a strong in vitro potency to attenuate the expression and function of the AR, further investigation will be required to determine whether this naturally occurring substance has in vivo potency to inhibit prostate cancer development. Copyright 2006 American Cancer Society.

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Year:  2006        PMID: 16691616     DOI: 10.1002/cncr.21935

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  18 in total

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2.  Comparative cellular and molecular analysis of cytotoxicity and apoptosis induction by doxorubicin and Baneh in human breast cancer T47D cells.

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3.  Gemcitabine combined with gum mastic causes potent growth inhibition and apoptosis of pancreatic cancer cells.

Authors:  Xin-yu Huang; Hong-cheng Wang; Zhou Yuan; Ang Li; Mei-lan He; Kai-xing Ai; Qi Zheng; Huan-long Qin
Journal:  Acta Pharmacol Sin       Date:  2010-06       Impact factor: 6.150

4.  Anti-inflammatory activity of Chios mastic gum is associated with inhibition of TNF-alpha induced oxidative stress.

Authors:  Angelike Triantafyllou; Alfiya Bikineyeva; Anna Dikalova; Rafal Nazarewicz; Stamatios Lerakis; Sergey Dikalov
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5.  Camphene, a plant-derived monoterpene, reduces plasma cholesterol and triglycerides in hyperlipidemic rats independently of HMG-CoA reductase activity.

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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.

Authors:  Heleni Loutrari; Sophia Magkouta; Andreas Papapetropoulos; Charis Roussos
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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