» Articles » PMID: 22198631

Biological Effect of Human Serum Collected Before and After Oral Intake of Pygeum Africanum on Various Benign Prostate Cell Cultures

Overview
Journal Asian J Androl
Specialty Urology
Date 2011 Dec 27
PMID 22198631
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Pygeum africanum (Tadenan) is a popular phytotherapeutic agent used in the treatment of symptomatic benign prostatic hyperplasia. The active compounds of the drug have not been identified, and determining the plasma concentration of the drug is, therefore, not possible. Because there are conflicting results on the efficacy of this drug, we aimed to investigate its effect on prostate cell growth in vitro using human serum collected before and after Pygeum africanum intake. We used primary and organotypic cultures of human prostatic stromal myofibroblast cell line WPMY and prostatic epithelial cell line PNT2. We also used fresh benign prostatic tissue. The serum of a treated man induced decreases in the proliferation of primary cells, organotypic cells and WPMY cells but not PNT2 cells. We also analysed the effect of treated serum on the gene expression profile of WPMY cells. The transcriptome analysis revealed an upregulation of genes involved in multiple tumour suppression pathways and a downregulation of genes involved in inflammation and oxidative-stress pathways. The oral intake of Pygeum africanum resulted in serum levels of active substances that were sufficient to inhibit the proliferation of cultured myofibroblasts prostatic cells. This inhibition was associated with changes in the transcriptome.

Citing Articles

Treatment of Benign Prostatic Hyperplasia by Natural Drugs.

Csikos E, Horvath A, Acs K, Papp N, Balazs V, Dolenc M Molecules. 2021; 26(23).

PMID: 34885733 PMC: 8659259. DOI: 10.3390/molecules26237141.


Effects of different natural extracts in an experimental model of benign prostatic hyperplasia (BPH).

Paterniti I, Campolo M, Cordaro M, Siracusa R, Filippone A, Esposito E Inflamm Res. 2018; 67(7):617-626.

PMID: 29679313 DOI: 10.1007/s00011-018-1152-9.


Ethanol Extract of Root of Inhibited the Growth of Liver Cancer Cell HepG2 by Inducing Cell Cycle Arrest and Migration Suppression.

Shen H, Wang H, Wang L, Wang L, Zhu M, Ming Y Evid Based Complement Alternat Med. 2017; 2017:8231936.

PMID: 29234432 PMC: 5660787. DOI: 10.1155/2017/8231936.


Effects of flavocoxid, a dual inhibitor of COX and 5-lipoxygenase enzymes, on benign prostatic hyperplasia.

Altavilla D, Minutoli L, Polito F, Irrera N, Arena S, Magno C Br J Pharmacol. 2012; 167(1):95-108.

PMID: 22471974 PMC: 3448916. DOI: 10.1111/j.1476-5381.2012.01969.x.

References
1.
Buck A . Is there a scientific basis for the therapeutic effects of serenoa repens in benign prostatic hyperplasia? Mechanisms of action. J Urol. 2004; 172(5 Pt 1):1792-9. DOI: 10.1097/01.ju.0000140503.11467.8e. View

2.
Boulbes D, Soustelle L, Costa P, Haddoum M, Bali J, Hollande F . Pygeum africanum extract inhibits proliferation of human cultured prostatic fibroblasts and myofibroblasts. BJU Int. 2006; 98(5):1106-13. DOI: 10.1111/j.1464-410X.2006.06483.x. View

3.
Takikawa M, Akiyama Y, Maruyama K, Suzuki A, Liu F, Tai S . Proteomic analysis of a highly metastatic gastric cancer cell line using two-dimensional differential gel electrophoresis. Oncol Rep. 2006; 16(4):705-11. View

4.
Madersbacher S, Alivizatos G, Nordling J, Rioja Sanz C, Emberton M, de la Rosette J . EAU 2004 guidelines on assessment, therapy and follow-up of men with lower urinary tract symptoms suggestive of benign prostatic obstruction (BPH guidelines). Eur Urol. 2004; 46(5):547-54. DOI: 10.1016/j.eururo.2004.07.016. View

5.
Cui H, Darmanin S, Natsuisaka M, Kondo T, Asaka M, Shindoh M . Enhanced expression of asparagine synthetase under glucose-deprived conditions protects pancreatic cancer cells from apoptosis induced by glucose deprivation and cisplatin. Cancer Res. 2007; 67(7):3345-55. DOI: 10.1158/0008-5472.CAN-06-2519. View