
Vol. 16, No. 1, 2009
Free Abstract
Article (PDF 380 KB)
Original Article · Originalarbeit
Phyllanthus urinaria Increases Apoptosis and Reduces Telomerase Activity in Human Nasopharyngeal Carcinoma Cells
Sheng-Teng Huanga, Chen-Yu Wangb, Rong-Chi Yangc, Chih-Ju Chua, Hsiao-Ting Wua, Jong-Hwei S. Pangd
a Department of Chinese Medicine, Chang Gung Memorial Hospital – Kaohsiung Medical Center, Chang Gung Institute of Technology, Taiwan, Republic of China b School of Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan, Republic of China c Chinese Herbal Pharmacy, Chang Gung Memorial Hospital, Tao-Yuan, Taiwan, Republic of China d Graduate Institute of Clinical Medical Sciences, Chang Gung University, Tao-Yuan, Taiwan, Republic of China
Address of Corresponding Author
Forsch Komplementmed 2009;16:34-40 (DOI: 10.1159/000194154)
Key Words
- Phyllanthus urinaria
- Apoptosis
- Bax/Bcl-2
- Telomerase activity
Summary
Background: This study was designed to obtain the chemical fingerprint and to investigate the effect of Phyllanthus urinaria on telomerase activity and apoptotic pathways in the human nasopharyngeal carcinoma cell line (NPC-BM1). Materials and Methods: The polyphenol compounds in P. urinaria were investigated by HPLC/MS. Cell viability with the treatment of P. urinaria, gallic acid, ellagic acid, quercetin and cisplatin was detected by MTT assay. TUNEL assay, DNA fragmentation analysis and caspase3 activity were used to confirm apoptotic changes. Telomerase activity was determined using the TRAP assay. RNA isolation and RT-PCR were used to analyze the related genes expression. All experiments on treatments with P. urinaria from 0–3 mg/ml were carried out for 24 h. Results: 5 major compounds including gallic acid, brevifolin carboxylic acid, corilagin, phyllanthusiin C and ellagic acid were identified as a plant fingerprint by HPLC/MS. With the MTT assay, we demonstrated that P. urinaria, gallic acid and ellagic acid reduce cell viability. The apoptosis features showed DNA fragmentation and increased caspase-3 activity associated with the down-regulation of Bcl-2, but not of Bax, p53, and PCNA (proliferating cell nuclear antigen) in P. urinaria-treated NPC-BM1 cells. Furthermore, treatment of NPC-BM1 cells led to an inhibition of hTERT (human telomerase reverse transcriptase), hTP1 (human telomerase-associated protein 1) and c-myc mRNA expression and to decreased telomerase activity. Conclusion: This study suggests that P. urinaria induces the death of NPC-BM1 cells in vitro through the induction of apoptosis and inhibited telomerase activity. Copyright © 2009 S. Karger AG, Basel
Author Contacts Dr. Sheng-Teng Huang, Department of Chinese Medicine, Chang Gung Memorial Hospital – Kaohsiung Medical Center, Chang Gung Institute of Technology, Taiwan, Republic of China, Tel. +886 7 7317123 ext. 2334, Fax 2335, sheng.teng@yahoo.com
Article Information
Published_online: February 6, 2009
Number of Print Pages : 7
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