Ethanol Extracts of Cornus alba Improve Benign Prostatic Hyperplasia by Inhibiting Prostate Cell Proliferation through Modulating 5 Alpha-Reductase/Androgen Receptor Axis-Mediated Signaling

被引:0
作者
Hwang, Byungdoo [1 ]
Kim, Jongyeob [1 ]
Park, Solbi [1 ]
Chung, Hyun Joo [2 ,3 ]
Kim, Hoon [1 ]
Choi, Yung Hyun [4 ]
Kim, Wun-Jae [5 ]
Myung, Soon Chul [2 ,3 ]
Jeong, Tae-Bin [6 ]
Kim, Kyung-Mi [6 ]
Jung, Jae-Chul [6 ]
Lee, Min-Won [7 ]
Kim, Jin Wook [8 ,9 ]
Moon, Sung-Kwon [1 ,3 ]
机构
[1] Chung Ang Univ, Dept Food & Nutr, 4726 Seodong Daero, Anseong 17546, South Korea
[2] Chung Ang Univ, Dept Urol, Coll Med, Seoul, South Korea
[3] Chung Ang Univ, Mol Biodesign Res Ctr, Coll Med, Seoul, South Korea
[4] Dong Eui Univ, Dept Biochem, Coll Oriental Med, Busan, South Korea
[5] Novarex Co Ltd, Inst Urotech, Cheongju, South Korea
[6] Novarex Co Ltd, Life Sci Res Inst, Cheongju, South Korea
[7] Chung Ang Univ, Coll Pharm, Lab Pharmacognosy & Nat Prod Derived Med, Seoul, South Korea
[8] Chung Ang Univ, Dept Med Informat, Coll Med, Seoul, South Korea
[9] Chung Ang Univ, Dept Urol, Gwangmyeong Hosp, 110 Deokan Ro, Gwangmyeong 14353, South Korea
基金
新加坡国家研究基金会;
关键词
Benign prostatic hyperplasia; BPH rat model; Ethanol extracts of Cornus alba; RWPE-1; WPMY-1; NF-KAPPA-B; ANDROGEN RECEPTOR; TRANSURETHRAL RESECTION; IN-VITRO; EXPRESSION; ANTHOCYANINS; DUTASTERIDE; GROWTH; CANCER; L;
D O I
暂无
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Purpose: The aim of this study was to investigate the efficacy of ethanol extracts of Cornus alba (ECA) against benign prostatic hyperplasia (BPH) in vitro and in vivo. Materials and Methods: The prostate stromal cells (WPMY-1) and epithelial cells (RWPE-1) were used to examine the action mechanism of ECA in BPH in vitro. ECA efficacy was evaluated in vivo using a testosterone propionate (TP)-induced BPH rat model. Results: Treatment with ECA inhibited the proliferation of prostate cells by inducing G1-phase cell cycle arrest through the regulation of positive and negative proteins. Treatment of prostate cells with ECA resulted in alterations in the mitogen-activated protein kinases and protein kinase B signaling pathways. The transcriptional binding activity of the NF-kappa B motif was suppressed in both ECA-treated prostate cells. In addition, treatment with ECA altered the level of BPH-associated axis markers (5 alpha-reductase, fibroblast growth factor-2, androgen receptor, epidermal growth factor, Bcl-2, and Bax) in both cell lines. Finally, the administration of ECA attenuated the enlargement of prostatic tissues in the TP-induced BPH rat model, accompanied by histology, immunoblot, and serum dihydrotestosterone levels. Conclusions: These results demonstrated that ECA exerted beneficial effects on BPH both in vitro and in vivo and might provide valuable information in the development of preventive or therapeutic agents for improving BPH.
引用
收藏
页码:830 / 841
页数:12
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